Mouse Monoclonal Antibody to VAMP8 (N-term)
货号：
P32781
别名：
Vesicle-associated membrane protein 8, VAMP-8, Endobrevin, EDB, VAMP8
应用：
WB,IHC
反应种属：
Human
抗体类型：
Primary antibody
Swissprot：
Q9BV40
规格：
目录价
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Description |
|---|
SNAREs, Soluble N-ethylmaleimide-sensitive factor- attachment protein receptors, are essential proteins for fusion of cellular membranes. SNAREs localized on opposing membranes assemble to form a trans-SNARE complex, an extended, parallel four alpha-helical bundle that drives membrane fusion. VAMP8 is a SNARE involved in autophagy through the direct control of autophagosome membrane fusion with the lysososome membrane. Also required for dense-granule secretion in platelets. Plays also a role in regulated enzyme secretion in pancreatic acinar cells. Involved in the abscission of the midbody during cell division, which leads to completely separate daughter cells. Involved in the homotypic fusion of early and late endosomes. |
Specification |
|
|---|---|
| Aliases | Vesicle-associated membrane protein 8, VAMP-8, Endobrevin, EDB, VAMP8 |
| Entrez GeneID | 8673 |
| Swissprot | Q9BV40 |
| WB Predicted band size | 11.4kDa |
| Host/Isotype | Mouse IgG1 |
| Antibody Type | Primary antibody |
| Storage | Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles. |
| Species Reactivity | Human |
| Immunogen | This VAMP8 antibody is generated from a mouse immunized with a KLH conjugated synthetic peptide between 2~24 amino acids from the N-terminal region of human VAMP8. |
Application |
|
|---|---|
| WB | 1/1000-1/2000 |
| IHC | 1/100-1/500 |
Product Image
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Western blot analysis of lysates from Hela, THP-1, A431 cell line (from left to right), using VAMP8 Antibody (N-term)(Cat. #P32781). P32781 was diluted at 1:1000 at each lane. A goat anti-mouse IgG H&L(HRP) at 1:10000 dilution was used as the secondary antibody. Lysates at 20μg per lane.
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Immunohistochemical analysis of paraffin-embedded H. brain section using VAMP8 Antibody (N-term)(Cat#P32781). P32781 was diluted at 1:25 dilution. A undiluted biotinylated goat polyvalent antibody was used as the secondary, followed by DAB staining.
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