Human/Mouse VAMP-2 Antibody Summary
Ser2-Lys94
Accession # P63027
Applications
Please Note: Optimal dilutions should be determined by each laboratory for each application. General Protocols are available in the Technical Information section on our website.
Scientific Data
Detection of Human and Mouse VAMP‑2 by Western Blot. Western blot shows lysates of Daudi human Burkitt's lymphoma cell line, Jurkat human acute T cell leukemia cell line, and mouse brain tissue. PVDF Membrane was probed with 0.1 µg/mL of Mouse Anti-Human/Mouse VAMP-2 Monoclonal Antibody (Catalog # MAB5136) followed by HRP-conjugated Anti-Mouse IgG Secondary Antibody (Catalog # HAF007). A specific band was detected for VAMP-2 at approximately 13 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 1.
Reconstitution Calculator
Preparation and Storage
- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 6 months, -20 to -70 °C under sterile conditions after reconstitution.
Background: VAMP-2
VAMP-2 (vesicle associated membrane protein 2; also Synaptobrevin-2) is a 13 kDa member of the Synaptobrevin family of proteins. It is a type IV transmembrane (TM) protein (i.e.- a type II TM protein whose C-terminus is almost completely transmembrane) that is found in the presynaptic terminals of neurons. VAMP-2 is targeted to presynaptic vesicles following binding to Synaptophysin I. Dissociation allows for synaptic vesicle fusion at the synaptic cleft with subsequent granule release. Human VAMP-2 is 116 amino acids (aa) in length. It contains one acetylation site at Ser2, a vSNARE coiled-coil homology region (aa 31‑91), and a membrane-anchor domain (aa 95‑114). Over aa 1‑94, human VAMP-2 shares 100% and 99% aa identity with canine and mouse VAMP-2, respectively.
Product Datasheets
Citations for Human/Mouse VAMP-2 Antibody
R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.
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Citations: Showing 1 - 4
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Organelle tethering, pore formation and SNARE compensation in the late endocytic pathway
Authors: LJ Davis, NA Bright, JR Edgar, MDJ Parkinson, L Wartosch, J Mantell, AA Peden, JP Luzio
Journal of Cell Science, 2021-05-27;134(10):.
Species: Human
Sample Types: Cell Lysates
Applications: Western Blot -
Prior exercise in humans redistributes intramuscular GLUT4 and enhances insulin-stimulated sarcolemmal and endosomal GLUT4 translocation
Authors: JR Knudsen, DE Steenberg, JR Hingst, LR Hodgson, C Henriquez-, Z Li, B Kiens, EA Richter, JFP Wojtaszews, P Verkade, TE Jensen
Mol Metab, 2020-04-17;0(0):100998.
Species: Mouse
Sample Types: Whole Tissue
Applications: IHC -
Ca(2+)-dependent Focal Exocytosis of Golgi-derived Vesicles Helps Phagocytic Uptake in Macrophages
Authors: N Vashi, SB Andrabi, S Ghanwat, M Suar, D Kumar
J. Biol. Chem, 2017-02-07;292(13):5144-5165.
Species: Human
Sample Types: Whole Cells
Applications: ICC -
Shiga toxin stimulates clathrin-independent endocytosis of the VAMP2, VAMP3 and VAMP8 SNARE proteins
Authors: Henri-François Renard, Maria Daniela Garcia-Castillo, Valérie Chambon, Christophe Lamaze, Ludger Johannes
Journal of Cell Science
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