| Code | CSB-RA843784A0HU |
| Size | US$210 |
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| Application | Recommended Dilution |
|---|---|
| WB | 1:500-1:2000 |
| FC | 1:50-1:200 |
VAMP8, also known as endobrevin, is a SNARE protein that plays essential roles in membrane fusion events critical to vesicular trafficking, autophagy, and regulated secretion. As a key mediator of endosomal and lysosomal fusion processes, VAMP8 has become an important target for researchers investigating autophagy pathways, platelet degranulation, mast cell exocytosis, and intracellular trafficking mechanisms.
This recombinant monoclonal antibody, generated from clone 2B8, offers the reproducibility and consistency that demanding experimental workflows require. Because the antibody sequence is defined and produced recombinantly in rabbit host cells, researchers benefit from lot-to-lot uniformity that eliminates the variability often encountered with traditional hybridoma-derived antibodies. Affinity chromatography purification ensures high specificity for your VAMP8 detection needs.
Validation studies demonstrate reliable performance across multiple applications and sample types. In western blot experiments, this antibody detects VAMP8 in a diverse panel of human cell lines including HL-60, MCF-7, SW620, K562, and HeLa cells, with cross-species reactivity confirmed in mouse NIH/3T3 cells as well as mouse liver and kidney tissue lysates. The observed band at approximately 15 kDa runs slightly higher than the predicted 11 kDa molecular weight, a shift commonly attributed to post-translational modifications such as glycosylation. Flow cytometry validation in HeLa cells confirms utility for intracellular protein detection in fixed and permeabilized samples, providing flexibility for researchers studying VAMP8 expression at the single-cell level.
Whether investigating autophagosome-lysosome fusion, secretory pathway dynamics, or immune cell degranulation, this antibody provides a dependable tool for advancing your understanding of VAMP8 biology.
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