Assay Kits

This product constitutes a ready-to-use microwell and strip plate ELISA (enzyme-linked immunosorbent assay) Kit designed for the assessment of the Telomerase Reverse Transcriptase (TERT) ELISA Kit target analytes within biological samples. The concentration gradients of the Kit standards or positive controls render a theoretical Kit detection range in biological research samples containing TERT. The ELISA analytical biochemical technique of the Kit is based on TERT antibody-TERT antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect TERT antigen targets in samples. It's important to note that this ELISA Kit is specifically tailored for detecting native, not recombinant TERT.

This product constitutes a ready-to-use microwell and strip plate ELISA (enzyme-linked immunosorbent assay) Kit designed for the assessment of the Telomerase Protein Component 1 (TEP1) ELISA Kit target analytes within biological samples. The concentration gradients of the Kit standards or positive controls render a theoretical Kit detection range in biological research samples containing TEP1. The ELISA analytical biochemical technique of the Kit is based on TEP1 antibody-TEP1 antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect TEP1 antigen targets in samples. It's important to note that this ELISA Kit is specifically tailored for detecting native, not recombinant TEP1.

This product constitutes a ready-to-use microwell and strip plate ELISA (enzyme-linked immunosorbent assay) Kit designed for the assessment of the TEL2, telomere maintenance 2, homolog (TELO2) ELISA Kit target analytes within biological samples. The concentration gradients of the Kit standards or positive controls render a theoretical Kit detection range in biological research samples containing TELO2. The ELISA analytical biochemical technique of the Kit is based on TELO2 antibody-TELO2 antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect TELO2 antigen targets in samples. It's important to note that this ELISA Kit is specifically tailored for detecting native, not recombinant TELO2.

This product constitutes a ready-to-use microwell and strip plate ELISA (enzyme-linked immunosorbent assay) Kit designed for the assessment of the Telomerase Protein Component 1 (TEP1) ELISA Kit target analytes within biological samples. The concentration gradients of the Kit standards or positive controls render a theoretical Kit detection range in biological research samples containing TEP1. The ELISA analytical biochemical technique of the Kit is based on TEP1 antibody-TEP1 antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect TEP1 antigen targets in samples. It's important to note that this ELISA Kit is specifically tailored for detecting native, not recombinant TEP1.

This product constitutes a ready-to-use microwell and strip plate ELISA (enzyme-linked immunosorbent assay) Kit designed for the assessment of the Telomerase Reverse Transcriptase (TERT) ELISA Kit target analytes within biological samples. The concentration gradients of the Kit standards or positive controls render a theoretical Kit detection range in biological research samples containing TERT. The ELISA analytical biochemical technique of the Kit is based on TERT antibody-TERT antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect TERT antigen targets in samples. It's important to note that this ELISA Kit is specifically tailored for detecting native, not recombinant TERT.

This ELISA Kit is designed for the quantitative assessment of Porcine TEP1 concentrations in serum, plasma, and other biological fluids through in vitro analysis. It employs the Sandwich-ELISA method. The micro ELISA plate provided in this Kit has been pre-coated with an antibody specific to TEP1. To conduct the assay, standards or samples are introduced into the respective micro ELISA plate wells and mixed with the specific antibody. Then a biotinylated detection antibody specific for TEP1 and Avidin-Horseradish Peroxidase (HRP) conjugate is added to each micro plate well successively and incubated. Unbound components are then thoroughly washed away. Following this, a substrate solution is introduced to each well. Only those wells that contain TEP1, biotinylated detection antibody and Avidin-HRP conjugate will appear blue in color. The enzymatic reaction with the substrate is halted by adding a sulfuric acid solution, causing the color to change to yellow. The optical density (OD) is quantitatively measured using a spectrophotometer at a wavelength of 450 nm +/- 2 nm. The OD value is proportional to the concentration of TEP1. You can determine the TEP1 concentration in the samples by comparing their OD to the standard curve provided.

This sandwich kit is designed for the precise quantitative detection of Rabbit Telomerase (also known as TE) in serum, plasma, cell culture supernates, cell lysates, tissue homogenates. This kit utilizes the Enzyme-Linked Immunosorbent Assay (ELISA) method. The plate has been pre-coated with Rabbit TE antibody. TE present in the sample is added and binds to antibodies coated on the wells. And then biotinylated Rabbit TE Antibody is added and binds to TE in the sample. Following this, Streptavidin-HRP is introduced and binds to the Biotinylated TE antibody. During a washing step, any unbound Streptavidin-HRP is removed. A substrate solution is then added, and color development occurs in proportion to the quantity of Rabbit TE. The reaction is halted by adding an acidic stop solution, and the absorbance is measured at 450 nm.

This product constitutes a ready-to-use microwell and strip plate ELISA (enzyme-linked immunosorbent assay) Kit designed for the assessment of the Telomerase Protein Component 1 (TEP1) ELISA Kit target analytes within biological samples. The concentration gradients of the Kit standards or positive controls render a theoretical Kit detection range in biological research samples containing TEP1. The ELISA analytical biochemical technique of the Kit is based on TEP1 antibody-TEP1 antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect TEP1 antigen targets in samples. It's important to note that this ELISA Kit is specifically tailored for detecting native, not recombinant TEP1.

This ELISA Kit is designed for the quantitative assessment of Rabbit TERT concentrations in serum, plasma, and other biological fluids through in vitro analysis. It employs the Sandwich-ELISA method. The micro ELISA plate provided in this Kit has been pre-coated with an antibody specific to TERT. To conduct the assay, standards or samples are introduced into the respective micro ELISA plate wells and mixed with the specific antibody. Then a biotinylated detection antibody specific for TERT and Avidin-Horseradish Peroxidase (HRP) conjugate is added to each micro plate well successively and incubated. Unbound components are then thoroughly washed away. Following this, a substrate solution is introduced to each well. Only those wells that contain TERT, biotinylated detection antibody and Avidin-HRP conjugate will appear blue in color. The enzymatic reaction with the substrate is halted by adding a sulfuric acid solution, causing the color to change to yellow. The optical density (OD) is quantitatively measured using a spectrophotometer at a wavelength of 450 nm +/- 2 nm. The OD value is proportional to the concentration of TERT. You can determine the TERT concentration in the samples by comparing their OD to the standard curve provided.

This Kit employs the Double Antibody Sandwich ELISA technique. The plate comes pre-coated with an anti-Rat TE monoclonal antibody, while the detection antibody is a biotinylated polyclonal antibody. Samples and biotinylated antibodies are added to ELISA plate wells and subsequently washed with PBS or TBS following their respective additions. Avidin-peroxidase conjugates are then introduced to the wells. Following a thorough wash with PBS or TBS, TMB substrate is utilized for color development. TMB reacts with peroxidase activity, resulting in the formation of a blue product, which ultimately turns yellow upon the addition of the stop solution (Color Reagent C). The intensity of the color and the quantity of the target analyte in the sample exhibit a positive correlation.

This product constitutes a ready-to-use microwell and strip plate ELISA (enzyme-linked immunosorbent assay) Kit designed for the assessment of the WD repeat containing, antisense to TP53 (WRAP53) ELISA Kit target analytes within biological samples. The concentration gradients of the Kit standards or positive controls render a theoretical Kit detection range in biological research samples containing WRAP53. The ELISA analytical biochemical technique of the Kit is based on WRAP53 antibody-WRAP53 antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect WRAP53 antigen targets in samples. It's important to note that this ELISA Kit is specifically tailored for detecting native, not recombinant WRAP53.

This product constitutes a ready-to-use microwell and strip plate ELISA (enzyme-linked immunosorbent assay) kit designed for the assessment of the Telomerase protein component 1 (Tep1) ELISA kit target analytes within biological samples. The concentration gradients of the kit standards or positive controls render a theoretical kit detection range in biological research samples containing Tep1. The ELISA analytical biochemical technique of the kit is based on Tep1 antibody-Tep1 antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect Tep1 antigen targets in samples. It's important to note that this ELISA kit is specifically tailored for detecting native, not recombinant Tep1.

This Kit is based on the sandwich enzyme-linked immunosorbent assay (ELISA) technology. Initially, anti-TCF7L2 antibody is pre-coated onto 96-well plates. Subsequently, biotin-conjugated anti-TCF7L2 antibody is employed as the detection antibody. The process involves adding standards, test samples, and the biotin-conjugated detection antibody to the wells, followed by a wash with a wash buffer. Next, HRP-Streptavidin is introduced, and any unbound conjugates are thoroughly washed away using the wash buffer. To visualize the HRP enzymatic reaction, TMB substrates are utilized. TMB undergoes catalysis by HRP, resulting in the generation of a blue-colored product that transitions to yellow upon the addition of an acidic stop solution. The intensity of the yellow color is directly proportional to the amount of TCF7L2 captured from the sample within the plate. The optical density (O.D.) absorbance at 450nm is then measured using a microplate reader, allowing for the calculation of the concentration of TCF7L2.

This TERT ELISA Kit is designed for the quantitative determination of Rat TERT and follows a solid-phase ELISA format. The TERT ELISA Kit employs a competitive enzyme immunoassay technique, utilizing a polyclonal anti-TERT antibody and a TERT-HRP conjugate. During the assay, the sample and buffer are incubated together with the TERT-HRP conjugate on a pre-coated plate for one hour. Following this incubation period, the wells are emptied and washed five times to remove any unbound substances. Next, the wells are incubated with a substrate for the HRP enzyme. The resulting enzyme-substrate reaction generates a blue-colored complex. To terminate the reaction, a stop solution is added, which subsequently changes the solution's color to yellow. The intensity of this yellow color is quantitatively measured spectrophotometrically at 450nm using a microplate reader. This color intensity is inversely proportional to the concentration of TERT, as TERT from the samples and TERT-HRP conjugate compete for binding sites on the anti-TERT antibody. Given the limited number of binding sites, as more sites are occupied by TERT from the sample, fewer sites are available to bind TERT-HRP conjugate. To determine the TERT concentration in each sample, a standard curve is constructed, correlating the intensity of the color (O.D.) to the concentration of standards. The TERT concentration in each sample can then be determined by interpolation from this standard curve.

This product constitutes a ready-to-use microwell and strip plate ELISA (enzyme-linked immunosorbent assay) Kit designed for the assessment of the Telomerase Protein Component 1 (TEP1) ELISA Kit target analytes within biological samples. The concentration gradients of the Kit standards or positive controls render a theoretical Kit detection range in biological research samples containing TEP1. The ELISA analytical biochemical technique of the Kit is based on TEP1 antibody-TEP1 antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect TEP1 antigen targets in samples. It's important to note that this ELISA Kit is specifically tailored for detecting native, not recombinant TEP1.

This product constitutes a ready-to-use microwell and strip plate ELISA (enzyme-linked immunosorbent assay) Kit designed for the assessment of the Telomerase Reverse Transcriptase (TERT) ELISA Kit target analytes within biological samples. The concentration gradients of the Kit standards or positive controls render a theoretical Kit detection range in biological research samples containing TERT. The ELISA analytical biochemical technique of the Kit is based on TERT antibody-TERT antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect TERT antigen targets in samples. It's important to note that this ELISA Kit is specifically tailored for detecting native, not recombinant TERT.

This product constitutes a ready-to-use microwell and strip plate ELISA (enzyme-linked immunosorbent assay) Kit designed for the assessment of the Telomerase (TERT) ELISA Kit target analytes within biological samples. The concentration gradients of the Kit standards or positive controls render a theoretical Kit detection range in biological research samples containing TERT. The ELISA analytical biochemical technique of the Kit is based on TERT antibody-TERT antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect TERT antigen targets in samples. It's important to note that this ELISA Kit is specifically tailored for detecting native, not recombinant TERT.

This product constitutes a ready-to-use microwell and strip plate ELISA (enzyme-linked immunosorbent assay) Kit designed for the assessment of the CST complex subunit CTC1 (C17orf68) ELISA Kit target analytes within biological samples. The concentration gradients of the Kit standards or positive controls render a theoretical Kit detection range in biological research samples containing C17orf68. The ELISA analytical biochemical technique of the Kit is based on C17orf68 antibody-C17orf68 antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect C17orf68 antigen targets in samples. It's important to note that this ELISA Kit is specifically tailored for detecting native, not recombinant C17orf68.

This product constitutes a ready-to-use microwell and strip plate ELISA (enzyme-linked immunosorbent assay) Kit designed for the assessment of the Protection of Telomeres 1 Homolog (POT1) ELISA Kit target analytes within biological samples. The concentration gradients of the Kit standards or positive controls render a theoretical Kit detection range in biological research samples containing POT1. The ELISA analytical biochemical technique of the Kit is based on POT1 antibody-POT1 antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect POT1 antigen targets in samples. It's important to note that this ELISA Kit is specifically tailored for detecting native, not recombinant POT1.

This product constitutes a ready-to-use microwell and strip plate ELISA (enzyme-linked immunosorbent assay) Kit designed for the assessment of the regulator of telomere elongation helicase 1 (RTEL1) ELISA Kit target analytes within biological samples. The concentration gradients of the Kit standards or positive controls render a theoretical Kit detection range in biological research samples containing RTEL1. The ELISA analytical biochemical technique of the Kit is based on RTEL1 antibody-RTEL1 antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect RTEL1 antigen targets in samples. It's important to note that this ELISA Kit is specifically tailored for detecting native, not recombinant RTEL1.