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Read our guarantee »Products:Neuroscience >> Neurotransmission >> Secretory Vesicles >> SNAPs & SNAREs
Anti-VAMP1 antibody
See all VAMP1 products (8) ...
Rabbit polyclonal to VAMP1
ICC/IF, IP, WB, IHC-Pmore details
Reacts with
Mouse, Rat, Dog, Human
Synthetic peptide: MSAPAQPPAEGTEGAAPG-C, corresponding to amino acids 1-18 of Rat VAMP1.
MSAPAQPPAE GTEGAAPG-C
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
PBS, 1 mg/ml BSA, 0.05% sodium azide
Concentration information loading...
Immunogen affinity purified
Polyclonal
IgG
Neuroscience >> Cell Type Marker >> Neuron marker >> Synapse marker
Signal Transduction >> Protein Trafficking >> Vesicle Transport >> SNAPs & SNAREs
Neuroscience >> Neurotransmission >> Secretory Vesicles >> Other
Neuroscience >> Neurotransmission >> Secretory Vesicles >> SNAPs & SNAREs
Our Abpromise guarantee covers the use of ab3346 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
ICC/IF: Use at an assay dependent dilution. (Used at a dilution of 1/1000 for 48 hrs incubation on mouse adult retina cells (see Abreview for further information).)
IP: Use at an assay dependent dilution.
WB: Use a concentration of 0.3 µg/ml(By Western blot, this antibody detects a 15 kDa protein representing VAMP 1 from rat brain whole protein extract.)
IHC-P: Use a concentration of 2 µg/mlPerform heat mediated antigen retrieval before commencing with IHC staining protocol.
Involved in the targeting and/or fusion of transport vesicles to their target membrane.
Nervous system, skeletal muscle and adipose tissue.
Belongs to the synaptobrevin family.
Contains 1 v-SNARE coiled-coil homology domain.
Mitochondrion outer membrane; Cytoplasmic vesicle > secretory vesicle > synaptic vesicle membrane. Cell junction > synapse > synaptosome and Cytoplasmic vesicle membrane. Cell junction > synapse > synaptosome.
Target information above from: UniProt accessionP23763
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Immunocytochemistry/ Immunofluorescence - VAMP1 antibody (ab3346)

ab3346 at a 1/1000 dilution staining mouse adult retina cells by ICC/IF. The cells were paraformaldehyde fixed and blocked with 5% serum prior to incubation with the antibody for 48 hours. Bound antibody was detected using an Alexa Fluor ® 488 conjugated donkey anti rabbit antibody. Dilutions of 1/1000 through to 1/5000 were found to work.
Staining in the outer plexiform layer was fainter than in the ganglion cell layer
This image is courtesy of an anonymous Abreview
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - VAMP1 antibody (ab3346)

ab3346 (2µg/ml) staining VAMP1 in human cerebral cortex using an automated system (DAKO Autostainer Plus). Using this protocol there is strong cytoplasmic and some membrane staining.
Sections were rehydrated and antigen retrieved with the Dako 3 in 1 AR buffer EDTA pH 9.0 in a DAKO PT link. Slides were peroxidase blocked in 3% H2O2 in methanol for 10 mins. They were then blocked with Dako Protein block for 10 minutes (containing casein 0.25% in PBS) then incubated with primary antibody for 20 min and detected with Dako envision flex amplification kit for 30 minutes. Colorimetric detection was completed with Diaminobenzidine for 5 minutes. Slides were counterstained with Haematoxylin and coverslipped under DePeX. Please note that, for manual staining, optimization of primary antibody concentration and incubation time is recommended. Signal amplification may be required.
This product has been referenced in:
See all 4 publications for this product
Publishing research using ab3346? Please let us know so that we can cite the reference in this datasheet
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ab3346 at a 1/1000 dilution staining mouse adult retina cells by ICC/IF. The cells were paraformaldehyde fixed and blocked with 5% serum prior to incubation with the antibody for 48 hours. Bound antibody was detected using an Alexa Fluor ® 488 conjugated donkey anti rabbit antibody. Dilutions of 1/1000 through to 1/5000 were found to work.
Staining in the outer plexiform layer was fainter than in the ganglion cell layer
This image is courtesy of an anonymous Abreview

ab3346 (2µg/ml) staining VAMP1 in human cerebral cortex using an automated system (DAKO Autostainer Plus). Using this protocol there is strong cytoplasmic and some membrane staining.
Sections were rehydrated and antigen retrieved with the Dako 3 in 1 AR buffer EDTA pH 9.0 in a DAKO PT link. Slides were peroxidase blocked in 3% H2O2 in methanol for 10 mins. They were then blocked with Dako Protein block for 10 minutes (containing casein 0.25% in PBS) then incubated with primary antibody for 20 min and detected with Dako envision flex amplification kit for 30 minutes. Colorimetric detection was completed with Diaminobenzidine for 5 minutes. Slides were counterstained with Haematoxylin and coverslipped under DePeX. Please note that, for manual staining, optimization of primary antibody concentration and incubation time is recommended. Signal amplification may be required.
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