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Anti-GAP43 Antibody (phospho-Ser41) LS-C214

Note: This antibody replaces LS-C7313, LS-C7314, LS-C7317, LS-C43076, LS-C49231, LS-C54363

Ordering

Wt. Vol. Conc. Price
- 100 µl - $355
Inquire for larger quantities

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Rabbit Polyclonal to Rat GAP43
Rat, Human, Mouse, Bovine, Dog, Chicken, Xenopus
Western blot
Unconjugated

Details

Rat GAP43
Rabbit
Rat, Human, Mouse, Bovine, Dog, Chicken, Xenopus (tested or 100% immunogen sequence identity)
Polyclonal
Immunoaffinity purified

Applications

Western blot (1:1000)

Specificity and Use

GAP43 antibody was raised against phosphopeptide corresponding to amino acid residues surrounding the phosphoSer4 of Gap-43.
pSer41
Specific for the ~50k Gap-43 protein phosphorylated at Ser41. In some tissues the antibody also recognizes a higher molecular weight protein that is also recognized by the pan Gap-43 antibody, that may be a Gap-43 aggregate or oligomer. Immunolabeling is blocked by the phosphopeptide used as antigen but not by the corresponding

Packaging

50 uL of 10 mM HEPES, pH 7.5, 150 mM sodium chloride, 0.1 mg/mL BSA, 50% glycerol.
Long term: -20°C; Short term: -20°C
For research use only.

About GAP43

P17677 NM_002045 NP_002036.1

GAP43 Antibody, Axonal membrane protein GAP-43 Antibody, B-50 Antibody, Growth associated protein 43 Antibody, Growth-associated protein 43 Antibody, Neural phosphoprotein B-50 Antibody, Neuromodulin Antibody, PP46 Antibody, GAP-43 Antibody, Protein F1 Antibody

This protein is associated with nerve growth. It is a major component of the motile "growth cones" that form the tips of elongating axons. Plays a role in axonal and dendritic filopodia induction.

Western blot

Western blot
Western blot of rat cortex lysate showing specific immunolabeling of the ~50k Gap-43 protein phosphorylated at Ser41 (Control). The phosphospecificity of this labeling is shown in the second lane (lambda-phosphatase: lambda phosphatase).

Western blot

Western blot
Western blot of rat cortex lysate showing specific immunolabeling of the ~50k Gap-43 protein phosphorylated at Ser41 (Control). The phosphospecificity of this labeling is shown in the second lane (lambda-phosphatase: l-Ptase). The blot is identical to the control except that it was incubated in l-Ptase (1200 units for 30 min) before being exposed to the Anti-Ser41 GAP-43. The immunolabeling is completely eliminated by treatment with l-Ptase.

Requested From: United States
Date Requested: 9/27/2016

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