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          • Primary Antibodies ›
          • RAB3GAP2 Antibodies
          The product (cat # {{productObj.productId}}) that you're looking for has been discontinued and replaced with {{productObj.replacementProductId}}. The product (cat # {{productObj.productId}}) that you're looking for has been discontinued. Please contact Technical Support with any questions.

          Invitrogen

          RAB3GAP2 Polyclonal Antibody

          View all (7) RAB3GAP2 antibodies
          Datasheet
          Protocols
          Datasheet
          Protocols

          Cite RAB3GAP2 Polyclonal Antibody

          Product Details

          PA5-55296

          Applications
          Tested Dilution
          Publications

          Immunohistochemistry (IHC)

          1:50-1:200
          -

          Immunocytochemistry (ICC/IF)

          0.25-2 µg/mL
          -
          Product Specifications

          Host/Isotype

          Rabbit / IgG

          Class

          Polyclonal

          Type

          Antibody

          Immunogen

          Recombinant protein corresponding to Human RAB3GAP2

          Conjugate

          Unconjugated Unconjugated Unconjugated

          Form

          Liquid

          Concentration

          0.1 mg/mL

          Storage conditions

          Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.

          Shipping conditions

          Wet ice

          RRID

          AB_2646245

          Product Specific Information

          Immunogen sequence: TYEIPRHPGV TEQNEELSIL YPAAIVTIDG FSLFQSLRAC RNQVAKAAAS GNENIQPPPL AYKKWGLQDI DTIIDHASVG IMTLSPFDQM KTA

          Highest antigen sequence identity to the following orthologs: Mouse - 99%, Rat - 99%.

          Target Information

          The protein encoded by this gene belongs to the RAB3 protein family, members of which are involved in regulated exocytosis of neurotransmitters and hormones. This protein forms the Rab3 GTPase-activating complex with RAB3GAP1, where it constitutes the regulatory subunit, whereas the latter functions as the catalytic subunit. This gene has the highest level of expression in the brain, consistent with it having a key role in neurodevelopment. Mutations in this gene are associated with Martsolf syndrome.

          For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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