Rabbit Anti-VAMP2 Recombinant Antibody (BA0117) (CBMAB-0937CQ)

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Basic Information

Host Animal
Rabbit
Clone
BA0117
Application
FC, IF, IP, WB
Immunogen
Human VAMP2 aa 1-100
Specificity
Human, Mouse, Rat
Antibody Isotype
IgG
Clonality
Monoclonal
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

Formulations & Storage [For reference only, actual COA shall prevail!]

Purity
>95% as determined by analysis by SDS-PAGE
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.
More Infomation

Target

Full Name
Vesicle Associated Membrane Protein 2
Introduction
The protein encoded by this gene is a member of the vesicle-associated membrane protein (VAMP)/synaptobrevin family. Involved in the targeting and/or fusion of transport vesicles to their target membrane. Modulates the gating characteristics of the delayed rectifier voltage-dependent potassium channel KCNB1.
Entrez Gene ID
Human6844
Mouse22318
Rat24803
UniProt ID
HumanP63027
MouseP63044
RatP63045
Alternative Names
SYB2; VAMP-2
Function
Involved in the targeting and/or fusion of transport vesicles to their target membrane (By similarity).
Major SNARE protein of synaptic vesicles which mediates fusion of synaptic vesicles to release neurotransmitters. Essential for fast vesicular exocytosis and activity-dependent neurotransmitter release as well as fast endocytosis that mediates rapid reuse of synaptic vesicles (By similarity) (PubMed:30929742).
Modulates the gating characteristics of the delayed rectifier voltage-dependent potassium channel KCNB1.
Biological Process
Biological Process calcium-ion regulated exocytosis Source:ParkinsonsUK-UCL
Biological Process cellular response to insulin stimulus Source:ParkinsonsUK-UCL
Biological Process eosinophil degranulation Source:UniProtKB1 Publication
Biological Process exocytosis Source:ParkinsonsUK-UCL1 Publication
Biological Process Golgi to plasma membrane protein transport Source:ParkinsonsUK-UCL
Biological Process long-term synaptic potentiation Source:ParkinsonsUK-UCL
Biological Process membrane fusion Source:ParkinsonsUK-UCL
Biological Process positive regulation of intracellular protein transport Source:ParkinsonsUK-UCL
Biological Process protein transport Source:ParkinsonsUK-UCL
Biological Process protein-containing complex assembly Source:ParkinsonsUK-UCL
Biological Process regulation of delayed rectifier potassium channel activity Source:UniProtKB
Biological Process regulation of exocytosis Source:ParkinsonsUK-UCL
Biological Process regulation of vesicle-mediated transport Source:ParkinsonsUK-UCL
Biological Process response to glucose Source:ParkinsonsUK-UCL
Biological Process SNARE complex assembly Source:GO_Central1 Publication
Biological Process synaptic vesicle endocytosis Source:UniProtKB
Biological Process synaptic vesicle exocytosis Source:ParkinsonsUK-UCL
Biological Process vesicle fusion Source:UniProtKB1 Publication
Biological Process vesicle-mediated transport Source:ParkinsonsUK-UCL
Cellular Location
Cytoplasmic vesicle, secretory vesicle, synaptic vesicle membrane
Cell membrane
Colocalizes with PRKCZ and WDFY2 in intracellular vesicles (PubMed:17313651).
Involvement in disease
Neurodevelopmental disorder with hypotonia and autistic features with or without hyperkinetic movements (NEDHAHM):
An autosomal dominant disorder characterized by axial hypotonia apparent at birth, global developmental delay, intellectual disability, seizures, and autistic features. Involuntary hyperkinetic movements are present in some patients.
Topology
Cytoplasmic: 2-94
Helical: 95-114
Vesicular: 115-116
PTM
Phosphorylated by PRKCZ in vitro and this phosphorylation is increased in the presence of WDFY2.
(Microbial infection) Targeted and hydrolyzed by C.botulinum neurotoxin type B (BoNT/B, botB) which hydrolyzes the 76-Gln-|-Phe-77 bond and probably inhibits neurotransmitter release (PubMed:7803399).
(Microbial infection) Targeted and hydrolyzed by C.botulinum neurotoxin type D (BoNT/D, botD) which probably hydrolyzes the 59-Lys-|-Leu-60 bond and inhibits neurotransmitter release (PubMed:22289120).
Note that humans are not known to be infected by C.botulinum type D.
(Microbial infection) Targeted and hydrolyzed by C.botulinum neurotoxin type F (BoNT/F, botF) which hydrolyzes the 58-Gln-|-Lys-59 bond and probably inhibits neurotransmitter release (PubMed:19543288).
(Microbial infection) Targeted and hydrolyzed by C.tetani tetanus toxin (tetX) which hydrolyzes the 76-Gln-|-Phe-77 bond and probably inhibits neurotransmitter release (PubMed:7803399).
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For research use only. Not intended for any clinical use.

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