GAPDH ELISA Kit
Quick Overview for GAPDH ELISA Kit (ABIN8068970)
Target
See all GAPDH ELISA KitsBinding Specificity
Reactivity
Detection Method
Method Type
Application
Sample Type
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Purpose
- S-Nitrosylated GAPDH ELISA Kit uses a modified 'biotin-switch' method to allow for the direct visualization of human, rat, and mouse S-Nitrosylated GAPDH by ELISA application.
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Analytical Method
- Quantitative
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Components
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- Size / Qty
- Anti-Pan-GAPDH Microplate
- 96 wells
- Positive Control
- HRP-Streptavidin
- 200 μL
- Wash Buffer
- Assay Diluent B
- Lysis Buffer
- TMB One-Step Substrate Reagent
- Stop Solution
- S-Nitrosylation Buffer A
- S-Nitrosylation Buffer B
- S-Nitrosylation Buffer C
- S-Nitrosylation Buffer D
- S-Nitrosylation Buffer E
- S-Nitrosylation Blocking Reagent
- S-Nitrosylation Reduction Reagent I
- S-Nitrosylation Reduction Reagent II
- S-Nitrosylation Labeling Reagent
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Material not included
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- Acetone (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
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Application Notes
- Optimal working dilution should be determined by the investigator.
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Plate
- Pre-coated
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Protocol
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- Prepare 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 Buffer containing 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-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.
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Restrictions
- For Research Use only
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Storage
- -20 °C
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Storage Comment
- The 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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- GAPDH (Glyceraldehyde-3-Phosphate Dehydrogenase (GAPDH))
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Alternative Name
- GAPDH
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Background
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Gene Symbols: GAPDH, GAPD, CDABP0047, OK/SW-cl.12
Background: The S-Nitrosylated GAPDH ELISA Kit uses a modified "biotin-switch" method to allow for the direct visualization of human and mouse S-Nitrosylated GAPDH 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 GAPDH antibody has been coated onto a 96-well plate. Biotinylated samples are pipetted into the wells and GAPDH 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 GAPDH. 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 GAPDH bound. The Stop Solution changes the color from blue to yellow, and the intensity of the color is measured at 450 nm.
Protein Name (Synonyms): Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) (EC 1.2.1.12) (Peptidyl-cysteine S-nitrosylase GAPDH) (EC 2.6.99.-)
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Gene ID
- 2597
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UniProt
- P04406
Target See all GAPDH ELISA Kits
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