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Syntaxin 1B antibody

The Rabbit Monoclonal anti-Syntaxin 1B antibody has been validated for WB, IHC and IF. It is suitable to detect Syntaxin 1B in samples from Human.
Catalog No. ABIN7270685

Quick Overview for Syntaxin 1B antibody (ABIN7270685)

Target

See all Syntaxin 1B (STX1B) Antibodies
Syntaxin 1B (STX1B)

Reactivity

  • 8
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 7
  • 1
  • 1
Rabbit

Clonality

  • 6
  • 3
Monoclonal

Conjugate

  • 9
This Syntaxin 1B antibody is un-conjugated

Application

  • 9
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Purpose

    Syntaxin Rabbit mAb

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    A synthesized peptide derived from human Syntaxin

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000,IHC,1:50 - 1:200,IF,1:50 - 1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.

    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

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    Syntaxin 1B (STX1B)

    Alternative Name

    STX1B

    Background

    The protein encoded by this gene belongs to a family of proteins thought to play a role in the exocytosis of synaptic vesicles. Vesicle exocytosis releases vesicular contents and is important to various cellular functions. For instance, the secretion of transmitters from neurons plays an important role in synaptic transmission. After exocytosis, the membrane and proteins from the vesicle are retrieved from the plasma membrane through the process of endocytosis. Mutations in this gene have been identified as one cause of fever-associated epilepsy syndromes. A possible link between this gene and Parkinson's disease has also been suggested. [provided by RefSeq, Jan 2015],GEFSP9, STX1B1, STX1B2,STX1B

    Molecular Weight

    33kDa

    Gene ID

    112755

    UniProt

    P61266
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