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GAPDH Rabbit Polyclonal Antibody (HRP)
Description
Research Area
Images & Validation
−| Tested Applications | WB |
|---|---|
| Dilution Range | Western blot, 0.02-0.1 μg/ml |
| Reactivity | Gallus, Human, Monkey, Mouse, Rat, Zebrafish |
Key Properties
−| Antibody Type | Primary Antibody |
|---|---|
| Host | Rabbit |
| Clonality | Polyclonal |
| Isotype | IgG |
| Immunogen | HRP-GAPDH antibody was raised against a synthetic peptide containing 16 amino acids near the carboxy terminus of GAPDH. |
| Target | 40S ribosomal protein S4, X isoform/Y isoform 1/Yisoform 2 |
| Molecular Weight | 36 kDa |
| Purification | HRP-GAPDH antibody is affinity chromatography purified via peptide column. |
| Conjugation | HRP |
Storage & Handling
−| Storage | HRP-GAPDH antibody can be stored at 4°C for three months and -20°C, stable for up to one year. |
|---|---|
| Form/Appearance | Liquid |
| Buffer/Preservatives | Each vial contains 50% glycerol, 0.9% NaCl, 0.2% Na2HPO4. |
| Concentration | 0.5 mg/mL |
| Disclaimer | For research use only |
Alternative Names
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Western blot analysis of GAPDH using anti-GAPDH antibody. Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: chicken heart tissue lysates, Lane 2: chicken liver tissue lysates, Lane 3: chicken brain tissue lysates, Lane 4: monkey heart tissue lysates, Lane 5: monkey lung tissue lysates, Lane 6: monkey kidney tissue lysates, Lane 7: monkey liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GAPDH antigen affinity purified polyclonal antibody at 0.1 µg/mL overnight at 4°C, then washed with TBS-0.1% Tween 3 times with 5 minutes each. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit with Tanon 5200 system. A specific band was detected for GAPDH at approximately 36 kDa. The expected band size for GAPDH is at 36 kDa.

Western blot analysis of GAPDH using anti-GAPDH antibody. Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human A562 whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat liver tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GAPDH antigen affinity purified polyclonal antibody at 0.1 µg/mL overnight at 4°C, then washed with TBS-0.1% Tween 3 times with 5 minutes each. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit with Tanon 5200 system. A specific band was detected for GAPDH at approximately 36 kDa. The expected band size for GAPDH is at 36 kDa.
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GAPDH Rabbit Polyclonal Antibody (HRP) (orb1804652)
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