SKU: WT144E Category:

U-Blot® S-Nitrosylated Fas and Total Fas ELISA Kit

$999.00

SKU: WT144E
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Product details

The S-Nitrosylated-Fas ELISA Kit uses a modified “biotin-switch” method to allow for the direct visualization of human S-Nitrosylated Fas by ELISA. In this S-Nitrosylation biotin switch assay, unmodified free cysteines are first blocked. S-Nitrosylated cysteines are then selectively reduced for specific labeling with biotin-maleimide reagents, which irreversibly bind to the cysteine thiol that was S-Nitrosylated. Biotinylation of the newly formed thiol groups can then be detected by ELISA. An anti-pan Fas antibody has been coated onto a 96-well plate. Biotinylated samples are pipetted into the wells and Fas present in a sample is bound to the wells by the immobilized antibody. The wells are washed and HRP-conjugated streptavidin is used to detect S-Nitrosylated Fas. The wells are again washed, a TMB substrate solution is added to the wells and color develops in proportion to the amount of S-Nitrosylated Fas bound. The Stop Solution changes the color from blue to yellow, and the intensity of the color is measured at 450 nm.This assay enables quick and easy quantification of target proteins and allows high-throughput screening of numerous different lysates without the need for traditional Western Blot analysis. It features minimal hands-on operation time, simple workflow, and completely non-radioactive detection system, ensuring safe and convenient experimental operation.

Specifications

Size1 Plate Kit, 2 Plate Kit, 5 Plate Kit
SpeciesHuman
Compatible Sample TypesTissue Lysates, Cell Lysates
Accession NumberP25445
Gene Id355
Gene SymbolsFAS, APT1, FAS1, TNFRSF6
Protein Name / SynonymsTumor necrosis factor receptor superfamily member 6; Apo-1 antigen; Apoptosis-mediating surface antigen FAS; FASLG receptor
Solid Support96-well Microplate
Design PrincipleSandwich-based
Method Of DetectionColorimetric
Research AreaPost-Translational Modifications, Nitrosylation, Epigenetics
ModificationS-Nitrosylation
Shipping Type2‑8 ℃
Storage-20°C
Kit ComponentsMicroplate Coated With Anti-Pan-Fas Antibody:1 plate;Positive Control:1 vial;HRP-Conjugated Streptavidin:200 μL;Wash Buffer:25 mL;Assay Diluent:15 mL;Lysis Buffer:5 mL;TMB One-Step Substrate Reagent:12 mL;Stop Solution:8 mL;S-Nitrosylation Buffer A:12 mL;S-Nitrosylation Buffer B:3 mL;S-Nitrosylation Buffer C:5 mL;S-Nitrosylation Buffer D:3 mL;S-Nitrosylation Buffer E:12 mL;S-Nitrosylation Blocking Reagent:2 vials;S-Nitrosylation Reduction Reagent I:2 vials;S-Nitrosylation Reduction Reagent II:2 vials;S-Nitrosylation Labeling Reagent:2 vials;
Additional Materials RequiredAcetone (pre-chilled (-20°C));Microplate reader capable of measuring absorbance at 450 nm;Protease and Phosphatase inhibitors;Precision pipettes to deliver 2 μL to 1 mL volumes;Adjustable 1-25 mL pipettes for reagent preparation;100 mL and 1 liter graduated cylinders;Log-log graph paper or computer and software for ELISA data analysis;Absorbent paper;Tubes to prepare positive control or sample dilutions;Distilled or deionized water;Shaker
Assay Procedure SummaryPrepare all reagents, samples and Positive Control as instructed; Block unmodified free cysteines using prepared S-Nitrosylation Blocking Buffer at 50°C with gentle rocking; Precipitate proteins with ice-cold acetone; Wash protein pellet twice with cold acetone/water mixture; Resuspend protein pellets in Buffers and adding Reducing and Labeling Reagents; Precipitate proteins with ice-cold acetone; Resuspend protein pellets; Add 100 μL sample and Positive Control to each well. Incubate 2.5 hours at room temperature or overnight at 4°C with gentle shaking; Add 100 μL prepared HRP-Conjugated Streptavidin solution. Incubate for 1 hour at room temperature with gentle shaking; Add 100 μL TMB One-Step Substrate Reagent to each well. Incubate 30 minutes at room temperature; Add 50 μL Stop Solution to each well. Read at 450 nm immediately.
Storage/StabilityThe entire kit may be stored at -20°C for up to 6 months from the date of shipment. Avoid repeated freeze-thaw cycles.
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