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Synaptotagmin antibody (AA 72-223)

This anti-Synaptotagmin antibody is a Mouse Monoclonal antibody detecting Synaptotagmin in WB. Suitable for Rat. This Primary Antibody has been cited in 5+ publications.
Catalog No. ABIN967965

Quick Overview for Synaptotagmin antibody (AA 72-223) (ABIN967965)

Target

See all Synaptotagmin (SYT) Antibodies
Synaptotagmin (SYT)

Reactivity

  • 38
  • 38
  • 23
  • 2
  • 1
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  • 1
Rat

Host

  • 38
  • 2
Mouse

Clonality

  • 38
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Monoclonal

Conjugate

  • 19
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  • 1
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  • 1
  • 1
  • 1
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  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Synaptotagmin antibody is un-conjugated

Application

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  • 6
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  • 2
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Western Blotting (WB)

Clone

BC17
  • Binding Specificity

    • 15
    • 10
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 72-223

    Cross-Reactivity

    Human

    Characteristics

    1. Since applications vary, each investigator should titrate the reagent to obtain optimal results.
    2. Please refer to us for technical protocols.
    3. Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before discarding to avoid accumulation of potentially explosive deposits in plumbing.
    4. Source of all serum proteins is from USDA inspected abattoirs located in the United States.

    Purification

    Purified from tissue culture supernatant or ascites by affinity chromatography.

    Immunogen

    Rat Synaptotagmin

    Isotype

    IgG1
  • Comment

    Related Products: ABIN968545, ABIN967389

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    250 µg/ml

    Buffer

    Aqueous buffered solution containing BSA, glycerol.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C
  • Liu, Fallon, Lashuel, Liu, Lansbury: "The UCH-L1 gene encodes two opposing enzymatic activities that affect alpha-synuclein degradation and Parkinson's disease susceptibility." in: Cell, Vol. 111, Issue 2, pp. 209-18, (2002) (PubMed).

    Ramalho-Santos, Moreno, Sutovsky, Chan, Hewitson, Wessel, Simerly, Schatten: "SNAREs in mammalian sperm: possible implications for fertilization." in: Developmental biology, Vol. 223, Issue 1, pp. 54-69, (2000) (PubMed).

    Duncan, Don-Wauchope, Tapechum, Shipston, Chow, Estibeiro: "High-efficiency Semliki Forest virus-mediated transduction in bovine adrenal chromaffin cells." in: The Biochemical journal, Vol. 342 Pt 3, pp. 497-501, (1999) (PubMed).

    Scheller: "Membrane trafficking in the presynaptic nerve terminal." in: Neuron, Vol. 14, Issue 5, pp. 893-7, (1995) (PubMed).

    Perin, Johnston, Ozcelik, Jahn, Francke, Südhof: "Structural and functional conservation of synaptotagmin (p65) in Drosophila and humans." in: The Journal of biological chemistry, Vol. 266, Issue 1, pp. 615-22, (1991) (PubMed).

  • Target

    Synaptotagmin (SYT)

    Alternative Name

    Synaptotagmin

    Background

    Synaptotagmin (p65) is an abundant synaptic vesicle protein that contains a single transmembrane region and two copies of an internal repeat that is homologous to the regulatory region of Protein Kinase C. It appears that synaptotagmin has a regulatory role in the synaptic vesicle pathway, particularly in vesicle docking and/or fusion with the plasmalemma. A model has been proposed to explain docking, activation, and fusion of synaptic vesicles with donor membranes. This model suggests that VAMP/synaptobrevin and synaptotagmin (vSNARE) on the synaptic vesicle, and SNAP-25 and syntaxin (tSNAREs) on the plasma membrane, interact to form a 7S complex. Two additional soluble proteins, alphaSNAP and NSF, are later added to the 7S complex, accompanied by the loss of synaptotagmin. The resulting 20S complex contains syntaxin, SNAP-25, VAMP, alphaSNAP, and NSF. Genetic studies in several species demonstrate that mutation or deletion of synaptotagmin results in a large decrease in Ca2+ triggered transmitter release. Mammalian synapses that lack synaptotagmin show a selective decrease in a fast component of release, suggesting that synaptotagmin is the Ca2+ sensor triggering exocytosis.

    Molecular Weight

    65 kDa
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