S R Group

The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human HbA1c. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human HbA1c. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Human HbA1c, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Human HbA1c in the samples is then determined by comparing the OD of the samples to the standard curve.

The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Mouse PDGFD. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Mouse PDGFD. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Mouse PDGFD, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Mouse PDGFD in the samples is then determined by comparing the OD of the samples to the standard curve.

The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human THRB. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human THRB. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Human THRB, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Human THRB in the samples is then determined by comparing the OD of the samples to the standard curve.

The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Mouse HMGCR. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Mouse HMGCR. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Mouse HMGCR, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Mouse HMGCR in the samples is then determined by comparing the OD of the samples to the standard curve.

This assay uses the quantitative enzyme immunoassay method. The provided microtiter plate in the kit is pre-coated with CSDE1 (Cold Shock Domain Containing Protein E1, RNA Binding). Standards or samples are added to the appropriate wells of the microtiter plate, along with a biotin-conjugated antibody specific to CSDE1 (Cold Shock Domain Containing Protein E1, RNA Binding). Then, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each well and incubated. Following this, TMB substrate solution is added. Only the wells that contain CSDE1 (Cold Shock Domain Containing Protein E1, RNA Binding), biotin-conjugated antibody, and enzyme-conjugated Avidin will show a color change. The enzyme-substrate reaction is stopped by adding a sulfuric acid solution, and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of CSDE1 (Cold Shock Domain Containing Protein E1, RNA Binding) in the samples is determined by comparing the optical density (OD) of the samples to the standard curve.

This ELISA kit uses quantitative-ELISA as the method. The Micro-elisa strip plate provided in this kit has been pre-coated with an antibody specific to a prolifeion inducing ligand (APRIL). Standards or samples are added to the appropriate Micro-elisa strip plate wells and combined to the specific antibody. Then a Horseradish Peroxidase (HRP)-conjugated antibody specific for a prolifeion inducing ligand (APRIL) is added to each Micro-elisa strip plate well and incubated. Free components are washed away. The TMB substrate solution is added to each well. Only those wells that contain a prolifeion inducing ligand (APRIL) and HRP conjugated a prolifeion inducing ligand (APRIL) antibody will appear blue in color and then turn yellow after the addition of the stop solution. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm. The OD value is proportional to the concentration of a prolifeion inducing ligand (APRIL). You can calculate the concentration of a prolifeion inducing ligand (APRIL) in the samples by comparing the OD of the samples to the standard curve.

This assay uses the quantitative enzyme immunoassay method. The provided microtiter plate in the kit is pre-coated with a1AT (Alpha-1-Antitrypsin). Standards or samples are added to the appropriate wells of the microtiter plate, along with a biotin-conjugated antibody specific to a1AT (Alpha-1-Antitrypsin). Then, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each well and incubated. Following this, TMB substrate solution is added. Only the wells that contain a1AT (Alpha-1-Antitrypsin), biotin-conjugated antibody, and enzyme-conjugated Avidin will show a color change. The enzyme-substrate reaction is stopped by adding a sulfuric acid solution, and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of a1AT (Alpha-1-Antitrypsin) in the samples is determined by comparing the optical density (OD) of the samples to the standard curve.

This assay uses the quantitative enzyme immunoassay method. The provided microtiter plate in the kit is pre-coated with a2M (Alpha-2-Macroglobulin). Standards or samples are added to the appropriate wells of the microtiter plate, along with a biotin-conjugated antibody specific to a2M (Alpha-2-Macroglobulin). Then, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each well and incubated. Following this, TMB substrate solution is added. Only the wells that contain a2M (Alpha-2-Macroglobulin), biotin-conjugated antibody, and enzyme-conjugated Avidin will show a color change. The enzyme-substrate reaction is stopped by adding a sulfuric acid solution, and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of a2M (Alpha-2-Macroglobulin) in the samples is determined by comparing the optical density (OD) of the samples to the standard curve.

This ELISA kit uses quantitative-ELISA as the method. The Micro-elisa strip plate provided in this kit has been pre-coated with an antibody specific to Acetyl Coenzyme A (A-CoA). Standards or samples are added to the appropriate Micro-elisa strip plate wells and combined to the specific antibody. Then a Horseradish Peroxidase (HRP)-conjugated antibody specific for Acetyl Coenzyme A (A-CoA) is added to each Micro-elisa strip plate well and incubated. Free components are washed away. The TMB substrate solution is added to each well. Only those wells that contain Acetyl Coenzyme A (A-CoA) and HRP conjugated Acetyl Coenzyme A (A-CoA) antibody will appear blue in color and then turn yellow after the addition of the stop solution. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm. The OD value is proportional to the concentration of Acetyl Coenzyme A (A-CoA). You can calculate the concentration of Acetyl Coenzyme A (A-CoA) in the samples by comparing the OD of the samples to the standard curve.

This ELISA kit uses quantitative-ELISA as the method. The Micro-elisa strip plate provided in this kit has been pre-coated with an antibody specific to Acetylcholine (ACH). Standards or samples are added to the appropriate Micro-elisa strip plate wells and combined to the specific antibody. Then a Horseradish Peroxidase (HRP)-conjugated antibody specific for Acetylcholine (ACH) is added to each Micro-elisa strip plate well and incubated. Free components are washed away. The TMB substrate solution is added to each well. Only those wells that contain Acetylcholine (ACH) and HRP conjugated Acetylcholine (ACH) antibody will appear blue in color and then turn yellow after the addition of the stop solution. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm. The OD value is proportional to the concentration of Acetylcholine (ACH). You can calculate the concentration of Acetylcholine (ACH) in the samples by comparing the OD of the samples to the standard curve.

This assay uses the quantitative enzyme immunoassay method. The provided microtiter plate in the kit is pre-coated with Anti-MBP (Anti-Myelin Basic Protein Antibody). Standards or samples are added to the appropriate wells of the microtiter plate, along with a biotin-conjugated antibody specific to Anti-MBP (Anti-Myelin Basic Protein Antibody) Then, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each well and incubated. Following this, TMB substrate solution is added. The enzyme-substrate reaction is stopped by adding a sulfuric acid solution, and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Anti-MBP (Anti-Myelin Basic Protein Antibody) in the samples is determined by comparing the optical density (OD) of the samples to the standard curve.

This ELISA kit uses quantitative-ELISA as the method. The Micro-elisa strip plate provided in this kit has been pre-coated with an antibody specific to Anti-Muellerian hormone type-2 receptor (AMHR2). Standards or samples are added to the appropriate Micro-elisa strip plate wells and combined to the specific antibody. Then a Horseradish Peroxidase (HRP)-conjugated antibody specific for Anti-Muellerian hormone type-2 receptor (AMHR2) is added to each Micro-elisa strip plate well and incubated. Free components are washed away. The TMB substrate solution is added to each well. Only those wells that contain Anti-Muellerian hormone type-2 receptor (AMHR2) and HRP conjugated Anti-Muellerian hormone type-2 receptor (AMHR2) antibody will appear blue in color and then turn yellow after the addition of the stop solution. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm. The OD value is proportional to the concentration of Anti-Muellerian hormone type-2 receptor (AMHR2). You can calculate the concentration of Anti-Muellerian hormone type-2 receptor (AMHR2) in the samples by comparing the OD of the samples to the standard curve.

The ELISA is based on the the qualitative immunoassay technique. The Microplate provided in this kit has been pre-coated with an Antibody specific to anti-muscarinic cholinergic receptor 3 (M3)-antibody, make it to solid-phase antibody. Samples are added to the Microplate wells and combined to the specific antibody. Then a Horseradish Peroxidase (HRP)-conjugated antibody specific for anti-muscarinic cholinergic receptor 3 (M3)-antibody is added to each Microplate well and incubated, so the antibody-antigen-Enzyme labeled antibody complex is formed. Following a wash to remove any unbound reagent, then the TMB substrate solution is added to each well. Only those wells that contain anti-muscarinic cholinergic receptor 3 (M3)-antibody and HRP-conjugated anti-muscarinic cholinergic receptor 3 (M3)-antibody antibody will appear blue in color and then turn yellow after the addition of the stop solution. The optical density (OD) is measured spectrophotometrically at a wave length of 450 nm. The qualitative determination of anti-muscarinic cholinergic receptor 3 (M3)-antibody is determined by comparing with the CUTOFF value.

This ELISA kit uses quantitative-ELISA as the method. The Micro-elisa strip plate provided in this kit has been pre-coated with an antibody specific to anti-mutated citrullinated vimentin (MCV) antibody. Standards or samples are added to the appropriate Micro-elisa strip plate wells and combined to the specific antibody. Then a Horseradish Peroxidase (HRP)-conjugated antibody specific for anti-mutated citrullinated vimentin (MCV) antibody is added to each Micro-elisa strip plate well and incubated. Free components are washed away. The TMB substrate solution is added to each well. Only those wells that contain anti-mutated citrullinated vimentin (MCV) antibody and HRP conjugated anti-mutated citrullinated vimentin (MCV) antibody antibody will appear blue in color and then turn yellow after the addition of the stop solution. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm. The OD value is proportional to the concentration of anti-mutated citrullinated vimentin (MCV) antibody. You can calculate the concentration of anti-mutated citrullinated vimentin (MCV) antibody in the samples by comparing the OD of the samples to the standard curve.

The ELISA is based on the the qualitative immunoassay technique. The Microplate provided in this kit has been pre-coated with an Antibody specific to Anti-nuclear Antibody (ANA), make it to solid-phase antibody. Samples are added to the Microplate wells and combined to the specific antibody. Then a Horseradish Peroxidase (HRP)-conjugated antibody specific for Anti-nuclear Antibody (ANA) is added to each Microplate well and incubated, so the antibody-antigen-Enzyme labeled antibody complex is formed. Following a wash to remove any unbound reagent, then the TMB substrate solution is added to each well. Only those wells that contain Anti-nuclear Antibody (ANA) and HRP-conjugated Anti-nuclear Antibody (ANA) antibody will appear blue in color and then turn yellow after the addition of the stop solution. The optical density (OD) is measured spectrophotometrically at a wave length of 450 nm. The qualitative determination of Anti-nuclear Antibody (ANA) is determined by comparing with the CUTOFF value.

The ELISA is based on the the qualitative immunoassay technique. The Microplate provided in this kit has been pre-coated with an Antibody specific to anti-ryanodine receptor calcium release channel antibodies, make it to solid-phase antibody. Samples are added to the Microplate wells and combined to the specific antibody. Then a Horseradish Peroxidase (HRP)-conjugated antibody specific for anti-ryanodine receptor calcium release channel antibodies is added to each Microplate well and incubated, so the antibody-antigen-Enzyme labeled antibody complex is formed. Following a wash to remove any unbound reagent, then the TMB substrate solution is added to each well. Only those wells that contain anti-ryanodine receptor calcium release channel antibodies and HRP-conjugated anti-ryanodine receptor calcium release channel antibodies antibody will appear blue in color and then turn yellow after the addition of the stop solution. The optical density (OD) is measured spectrophotometrically at a wave length of 450 nm. The qualitative determination of anti-ryanodine receptor calcium release channel antibodies is determined by comparing with the CUTOFF value.

The ELISA is based on the the qualitative immunoassay technique. The Microplate provided in this kit has been pre-coated with an Antibody specific to anti-ryanodine antibody, make it to solid-phase antibody. Samples are added to the Microplate wells and combined to the specific antibody. Then a Horseradish Peroxidase (HRP)-conjugated antibody specific for anti-ryanodine antibody is added to each Microplate well and incubated, so the antibody-antigen-Enzyme labeled antibody complex is formed. Following a wash to remove any unbound reagent, then the TMB substrate solution is added to each well. Only those wells that contain anti-ryanodine antibody and HRP-conjugated anti-ryanodine antibody antibody will appear blue in color and then turn yellow after the addition of the stop solution. The optical density (OD) is measured spectrophotometrically at a wave length of 450 nm. The qualitative determination of anti-ryanodine antibody is determined by comparing with the CUTOFF value.

The ELISA is based on the the qualitative immunoassay technique. The Microplate provided in this kit has been pre-coated with an Antibody specific to anti-Survivin antibody (Surv), make it to solid-phase antibody. Samples are added to the Microplate wells and combined to the specific antibody. Then a Horseradish Peroxidase (HRP)-conjugated antibody specific for anti-Survivin antibody (Surv) is added to each Microplate well and incubated, so the antibody-antigen-Enzyme labeled antibody complex is formed. Following a wash to remove any unbound reagent, then the TMB substrate solution is added to each well. Only those wells that contain anti-Survivin antibody (Surv) and HRP-conjugated anti-Survivin antibody (Surv) antibody will appear blue in color and then turn yellow after the addition of the stop solution. The optical density (OD) is measured spectrophotometrically at a wave length of 450 nm. The qualitative determination of anti-Survivin antibody (Surv) is determined by comparing with the CUTOFF value.

The ELISA is based on the the qualitative immunoassay technique. The Microplate provided in this kit has been pre-coated with an Antibody specific to anti-thrombin receptor (ATR), make it to solid-phase antibody. Samples are added to the Microplate wells and combined to the specific antibody. Then a Horseradish Peroxidase (HRP)-conjugated antibody specific for anti-thrombin receptor (ATR) is added to each Microplate well and incubated, so the antibody-antigen-Enzyme labeled antibody complex is formed. Following a wash to remove any unbound reagent, then the TMB substrate solution is added to each well. Only those wells that contain anti-thrombin receptor (ATR) and HRP-conjugated anti-thrombin receptor (ATR) antibody will appear blue in color and then turn yellow after the addition of the stop solution. The optical density (OD) is measured spectrophotometrically at a wave length of 450 nm. The qualitative determination of anti-thrombin receptor (ATR) is determined by comparing with the CUTOFF value.

The ELISA is based on the the qualitative immunoassay technique. The Microplate provided in this kit has been pre-coated with an Antibody specific to anti-thrombopoietin autoantibody (IgG), make it to solid-phase antibody. Samples are added to the Microplate wells and combined to the specific antibody. Then a Horseradish Peroxidase (HRP)-conjugated antibody specific for anti-thrombopoietin autoantibody (IgG) is added to each Microplate well and incubated, so the antibody-antigen-Enzyme labeled antibody complex is formed. Following a wash to remove any unbound reagent, then the TMB substrate solution is added to each well. Only those wells that contain anti-thrombopoietin autoantibody (IgG) and HRP-conjugated anti-thrombopoietin autoantibody (IgG) antibody will appear blue in color and then turn yellow after the addition of the stop solution. The optical density (OD) is measured spectrophotometrically at a wave length of 450 nm. The qualitative determination of anti-thrombopoietin autoantibody (IgG) is determined by comparing with the CUTOFF value.

This ELISA kit uses quantitative-ELISA as the method. The Micro-elisa strip plate provided in this kit has been pre-coated with an antibody specific to APOH (Apolipoprotein H). Standards or samples are added to the appropriate Micro-elisa strip plate wells and combined to the specific antibody. Then a Horseradish Peroxidase (HRP)-conjugated antibody specific for APOH (Apolipoprotein H) is added to each Micro-elisa strip plate well and incubated. Free components are washed away. The TMB substrate solution is added to each well. Only those wells that contain APOH (Apolipoprotein H) and HRP conjugated APOH (Apolipoprotein H) antibody will appear blue in color and then turn yellow after the addition of the stop solution. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm. The OD value is proportional to the concentration of APOH (Apolipoprotein H). You can calculate the concentration of APOH (Apolipoprotein H) in the samples by comparing the OD of the samples to the standard curve.

This assay uses the quantitative enzyme immunoassay method. The provided microtiter plate in the kit is pre-coated with APOL1 (Apolipoprotein L). Standards or samples are added to the appropriate wells of the microtiter plate, along with a biotin-conjugated antibody specific to APOL1 (Apolipoprotein L). Then, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each well and incubated. Following this, TMB substrate solution is added. Only the wells that contain APOL1 (Apolipoprotein L), biotin-conjugated antibody, and enzyme-conjugated Avidin will show a color change. The enzyme-substrate reaction is stopped by adding a sulfuric acid solution, and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of APOL1 (Apolipoprotein L) in the samples is determined by comparing the optical density (OD) of the samples to the standard curve.

This ELISA kit uses quantitative-ELISA as the method. The Micro-elisa strip plate provided in this kit has been pre-coated with an antibody specific to Apolipoprotein M (APO-M). Standards or samples are added to the appropriate Micro-elisa strip plate wells and combined to the specific antibody. Then a Horseradish Peroxidase (HRP)-conjugated antibody specific for Apolipoprotein M (APO-M) is added to each Micro-elisa strip plate well and incubated. Free components are washed away. The TMB substrate solution is added to each well. Only those wells that contain Apolipoprotein M (APO-M) and HRP conjugated Apolipoprotein M (APO-M) antibody will appear blue in color and then turn yellow after the addition of the stop solution. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm. The OD value is proportional to the concentration of Apolipoprotein M (APO-M). You can calculate the concentration of Apolipoprotein M (APO-M) in the samples by comparing the OD of the samples to the standard curve.

This ELISA kit uses quantitative-ELISA as the method. The Micro-elisa strip plate provided in this kit has been pre-coated with an antibody specific to Apoptosis-associated speck-like protein containing a CARD (PYCARD). Standards or samples are added to the appropriate Micro-elisa strip plate wells and combined to the specific antibody. Then a Horseradish Peroxidase (HRP)-conjugated antibody specific for Apoptosis-associated speck-like protein containing a CARD (PYCARD) is added to each Micro-elisa strip plate well and incubated. Free components are washed away. The TMB substrate solution is added to each well. Only those wells that contain Apoptosis-associated speck-like protein containing a CARD (PYCARD) and HRP conjugated Apoptosis-associated speck-like protein containing a CARD (PYCARD) antibody will appear blue in color and then turn yellow after the addition of the stop solution. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm. The OD value is proportional to the concentration of Apoptosis-associated speck-like protein containing a CARD (PYCARD). You can calculate the concentration of Apoptosis-associated speck-like protein containing a CARD (PYCARD) in the samples by comparing the OD of the samples to the standard curve.

This ELISA kit uses quantitative-ELISA as the method. The Micro-elisa strip plate provided in this kit has been pre-coated with an antibody specific to Arylacetamide deacetylase-like 2 (AADACL2). Standards or samples are added to the appropriate Micro-elisa strip plate wells and combined to the specific antibody. Then a Horseradish Peroxidase (HRP)-conjugated antibody specific for Arylacetamide deacetylase-like 2 (AADACL2) is added to each Micro-elisa strip plate well and incubated. Free components are washed away. The TMB substrate solution is added to each well. Only those wells that contain Arylacetamide deacetylase-like 2 (AADACL2) and HRP conjugated Arylacetamide deacetylase-like 2 (AADACL2) antibody will appear blue in color and then turn yellow after the addition of the stop solution. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm. The OD value is proportional to the concentration of Arylacetamide deacetylase-like 2 (AADACL2). You can calculate the concentration of Arylacetamide deacetylase-like 2 (AADACL2) in the samples by comparing the OD of the samples to the standard curve.

This ELISA kit uses quantitative-ELISA as the method. The Micro-elisa strip plate provided in this kit has been pre-coated with an antibody specific to Arylesterase (ARY). Standards or samples are added to the appropriate Micro-elisa strip plate wells and combined to the specific antibody. Then a Horseradish Peroxidase (HRP)-conjugated antibody specific for Arylesterase (ARY) is added to each Micro-elisa strip plate well and incubated. Free components are washed away. The TMB substrate solution is added to each well. Only those wells that contain Arylesterase (ARY) and HRP conjugated Arylesterase (ARY) antibody will appear blue in color and then turn yellow after the addition of the stop solution. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm. The OD value is proportional to the concentration of Arylesterase (ARY). You can calculate the concentration of Arylesterase (ARY) in the samples by comparing the OD of the samples to the standard curve.

This ELISA kit uses quantitative-ELISA as the method. The Micro-elisa strip plate provided in this kit has been pre-coated with an antibody specific to Ascorbate Peroxidase (APX). Standards or samples are added to the appropriate Micro-elisa strip plate wells and combined to the specific antibody. Then a Horseradish Peroxidase (HRP)-conjugated antibody specific for Ascorbate Peroxidase (APX) is added to each Micro-elisa strip plate well and incubated. Free components are washed away. The TMB substrate solution is added to each well. Only those wells that contain Ascorbate Peroxidase (APX) and HRP conjugated Ascorbate Peroxidase (APX) antibody will appear blue in color and then turn yellow after the addition of the stop solution. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm. The OD value is proportional to the concentration of Ascorbate Peroxidase (APX). You can calculate the concentration of Ascorbate Peroxidase (APX) in the samples by comparing the OD of the samples to the standard curve.

This assay uses the quantitative enzyme immunoassay method. The provided microtiter plate in the kit is pre-coated with ATM (Ataxia Telangiectasia Mutated). Standards or samples are added to the appropriate wells of the microtiter plate, along with a biotin-conjugated antibody specific to ATM (Ataxia Telangiectasia Mutated). Then, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each well and incubated. Following this, TMB substrate solution is added. Only the wells that contain ATM (Ataxia Telangiectasia Mutated), biotin-conjugated antibody, and enzyme-conjugated Avidin will show a color change. The enzyme-substrate reaction is stopped by adding a sulfuric acid solution, and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of ATM (Ataxia Telangiectasia Mutated) in the samples is determined by comparing the optical density (OD) of the samples to the standard curve.

The ELISA is based on the the qualitative immunoassay technique. The Microplate provided in this kit has been pre-coated with an Antibody specific to Atopic Dermatitis (AD), make it to solid-phase antibody. Samples are added to the Microplate wells and combined to the specific antibody. Then a Horseradish Peroxidase (HRP)-conjugated antibody specific for Atopic Dermatitis (AD) is added to each Microplate well and incubated, so the antibody-antigen-Enzyme labeled antibody complex is formed. Following a wash to remove any unbound reagent, then the TMB substrate solution is added to each well. Only those wells that contain Atopic Dermatitis (AD) and HRP-conjugated Atopic Dermatitis (AD) antibody will appear blue in color and then turn yellow after the addition of the stop solution. The optical density (OD) is measured spectrophotometrically at a wave length of 450 nm. The qualitative determination of Atopic Dermatitis (AD) is determined by comparing with the CUTOFF value.

This ELISA kit uses quantitative-ELISA as the method. The Micro-elisa strip plate provided in this kit has been pre-coated with an antibody specific to ATP synthase lipid-binding protein, mitochondrial (ATP5G1). Standards or samples are added to the appropriate Micro-elisa strip plate wells and combined to the specific antibody. Then a Horseradish Peroxidase (HRP)-conjugated antibody specific for ATP synthase lipid-binding protein, mitochondrial (ATP5G1) is added to each Micro-elisa strip plate well and incubated. Free components are washed away. The TMB substrate solution is added to each well. Only those wells that contain ATP synthase lipid-binding protein, mitochondrial (ATP5G1) and HRP conjugated ATP synthase lipid-binding protein, mitochondrial (ATP5G1) antibody will appear blue in color and then turn yellow after the addition of the stop solution. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm. The OD value is proportional to the concentration of ATP synthase lipid-binding protein, mitochondrial (ATP5G1). You can calculate the concentration of ATP synthase lipid-binding protein, mitochondrial (ATP5G1) in the samples by comparing the OD of the samples to the standard curve.

This assay uses the quantitative enzyme immunoassay method. The provided microtiter plate in the kit is pre-coated with ATRN (Attractin). Standards or samples are added to the appropriate wells of the microtiter plate, along with a biotin-conjugated antibody specific to ATRN (Attractin). Then, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each well and incubated. Following this, TMB substrate solution is added. Only the wells that contain ATRN (Attractin), biotin-conjugated antibody, and enzyme-conjugated Avidin will show a color change. The enzyme-substrate reaction is stopped by adding a sulfuric acid solution, and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of ATRN (Attractin) in the samples is determined by comparing the optical density (OD) of the samples to the standard curve.

This ELISA kit uses quantitative-ELISA as the method. The Micro-elisa strip plate provided in this kit has been pre-coated with an antibody specific to B-and T-lymphocyte attenuator (BTLA). Standards or samples are added to the appropriate Micro-elisa strip plate wells and combined to the specific antibody. Then a Horseradish Peroxidase (HRP)-conjugated antibody specific for B-and T-lymphocyte attenuator (BTLA) is added to each Micro-elisa strip plate well and incubated. Free components are washed away. The TMB substrate solution is added to each well. Only those wells that contain B-and T-lymphocyte attenuator (BTLA) and HRP conjugated B-and T-lymphocyte attenuator (BTLA) antibody will appear blue in color and then turn yellow after the addition of the stop solution. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm. The OD value is proportional to the concentration of B-and T-lymphocyte attenuator (BTLA). You can calculate the concentration of B-and T-lymphocyte attenuator (BTLA) in the samples by comparing the OD of the samples to the standard curve.

This ELISA kit uses quantitative-ELISA as the method. The Micro-elisa strip plate provided in this kit has been pre-coated with an antibody specific to bactericidal/permeabilityincreasingprotein (BPI). Standards or samples are added to the appropriate Micro-elisa strip plate wells and combined to the specific antibody. Then a Horseradish Peroxidase (HRP)-conjugated antibody specific for bactericidal/permeabilityincreasingprotein (BPI) is added to each Micro-elisa strip plate well and incubated. Free components are washed away. The TMB substrate solution is added to each well. Only those wells that contain bactericidal/permeabilityincreasingprotein (BPI) and HRP conjugated bactericidal/permeabilityincreasingprotein (BPI) antibody will appear blue in color and then turn yellow after the addition of the stop solution. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm. The OD value is proportional to the concentration of bactericidal/permeabilityincreasingprotein (BPI). You can calculate the concentration of bactericidal/permeabilityincreasingprotein (BPI) in the samples by comparing the OD of the samples to the standard curve.

This ELISA kit uses quantitative-ELISA as the method. The Micro-elisa strip plate provided in this kit has been pre-coated with an antibody specific to Beta-1 adrenergic receptor (ADRB1). Standards or samples are added to the appropriate Micro-elisa strip plate wells and combined to the specific antibody. Then a Horseradish Peroxidase (HRP)-conjugated antibody specific for Beta-1 adrenergic receptor (ADRB1) is added to each Micro-elisa strip plate well and incubated. Free components are washed away. The TMB substrate solution is added to each well. Only those wells that contain Beta-1 adrenergic receptor (ADRB1) and HRP conjugated Beta-1 adrenergic receptor (ADRB1) antibody will appear blue in color and then turn yellow after the addition of the stop solution. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm. The OD value is proportional to the concentration of Beta-1 adrenergic receptor (ADRB1). You can calculate the concentration of Beta-1 adrenergic receptor (ADRB1) in the samples by comparing the OD of the samples to the standard curve.

This ELISA kit uses quantitative-ELISA as the method. The Micro-elisa strip plate provided in this kit has been pre-coated with an antibody specific to Brain-specific serine protease 4 (PRSS22). Standards or samples are added to the appropriate Micro-elisa strip plate wells and combined to the specific antibody. Then a Horseradish Peroxidase (HRP)-conjugated antibody specific for Brain-specific serine protease 4 (PRSS22) is added to each Micro-elisa strip plate well and incubated. Free components are washed away. The TMB substrate solution is added to each well. Only those wells that contain Brain-specific serine protease 4 (PRSS22) and HRP conjugated Brain-specific serine protease 4 (PRSS22) antibody will appear blue in color and then turn yellow after the addition of the stop solution. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm. The OD value is proportional to the concentration of Brain-specific serine protease 4 (PRSS22). You can calculate the concentration of Brain-specific serine protease 4 (PRSS22) in the samples by comparing the OD of the samples to the standard curve.

This ELISA kit uses quantitative-ELISA as the method. The Micro-elisa strip plate provided in this kit has been pre-coated with an antibody specific to Bromodeoxyuridine (BrdU). Standards or samples are added to the appropriate Micro-elisa strip plate wells and combined to the specific antibody. Then a Horseradish Peroxidase (HRP)-conjugated antibody specific for Bromodeoxyuridine (BrdU) is added to each Micro-elisa strip plate well and incubated. Free components are washed away. The TMB substrate solution is added to each well. Only those wells that contain Bromodeoxyuridine (BrdU) and HRP conjugated Bromodeoxyuridine (BrdU) antibody will appear blue in color and then turn yellow after the addition of the stop solution. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm. The OD value is proportional to the concentration of Bromodeoxyuridine (BrdU). You can calculate the concentration of Bromodeoxyuridine (BrdU) in the samples by comparing the OD of the samples to the standard curve.

This assay uses the quantitative enzyme immunoassay method. The provided microtiter plate in the kit is pre-coated with BSDL (Lipase, Bile Salt Dependent). Standards or samples are added to the appropriate wells of the microtiter plate, along with a biotin-conjugated antibody specific to BSDL (Lipase, Bile Salt Dependent). Then, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each well and incubated. Following this, TMB substrate solution is added. Only the wells that contain BSDL (Lipase, Bile Salt Dependent), biotin-conjugated antibody, and enzyme-conjugated Avidin will show a color change. The enzyme-substrate reaction is stopped by adding a sulfuric acid solution, and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of BSDL (Lipase, Bile Salt Dependent) in the samples is determined by comparing the optical density (OD) of the samples to the standard curve.

This assay uses the quantitative enzyme immunoassay method. The provided microtiter plate in the kit is pre-coated with BTN1A1 (Butyrophilin Subfamily 1, Member A1). Standards or samples are added to the appropriate wells of the microtiter plate, along with a biotin-conjugated antibody specific to BTN1A1 (Butyrophilin Subfamily 1, Member A1). Then, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each well and incubated. Following this, TMB substrate solution is added. Only the wells that contain BTN1A1 (Butyrophilin Subfamily 1, Member A1), biotin-conjugated antibody, and enzyme-conjugated Avidin will show a color change. The enzyme-substrate reaction is stopped by adding a sulfuric acid solution, and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of BTN1A1 (Butyrophilin Subfamily 1, Member A1) in the samples is determined by comparing the optical density (OD) of the samples to the standard curve.

This ELISA kit uses quantitative-ELISA as the method. The Micro-elisa strip plate provided in this kit has been pre-coated with an antibody specific to Carboxypeptidase B (CPB1). Standards or samples are added to the appropriate Micro-elisa strip plate wells and combined to the specific antibody. Then a Horseradish Peroxidase (HRP)-conjugated antibody specific for Carboxypeptidase B (CPB1) is added to each Micro-elisa strip plate well and incubated. Free components are washed away. The TMB substrate solution is added to each well. Only those wells that contain Carboxypeptidase B (CPB1) and HRP conjugated Carboxypeptidase B (CPB1) antibody will appear blue in color and then turn yellow after the addition of the stop solution. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm. The OD value is proportional to the concentration of Carboxypeptidase B (CPB1). You can calculate the concentration of Carboxypeptidase B (CPB1) in the samples by comparing the OD of the samples to the standard curve.