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BIN1 antibody (AA 543-593)

This anti-BIN1 antibody is a Rabbit Polyclonal antibody detecting BIN1 in WB, IP and IHC (fp). Suitable for Human.
Catalog No. ABIN7454858

Quick Overview for BIN1 antibody (AA 543-593) (ABIN7454858)

Target

See all BIN1 Antibodies
BIN1 (Bridging Integrator 1 (BIN1))

Reactivity

  • 51
  • 28
  • 19
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Human

Host

  • 35
  • 17
  • 1
Rabbit

Clonality

  • 32
  • 21
Polyclonal

Conjugate

  • 44
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This BIN1 antibody is un-conjugated

Application

  • 41
  • 24
  • 19
  • 14
  • 13
  • 11
  • 8
  • 5
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunoprecipitation (IP), Immunohistochemistry (Formalin-fixed Paraffin-embedded Sections) (IHC (fp))
  • Binding Specificity

    • 7
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 543-593

    Purpose

    Rabbit anti-Bin1 Antibody, Affinity Purified

    Purification

    Affinity Purified

    Immunogen

    between AA 543 and 593

    Isotype

    IgG
  • Application Notes

    IHC: 1:500 - 1:2,000. Epitope retrieval with citrate buffer pH 6.0 is recommended for FFPE tissue sections.

    IP: 2 - 10 μg/mg lysate

    WB: 1:500 - 1:2,500

    Restrictions

    For Research Use only
  • Concentration

    1000 μg/mL

    Buffer

    Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % Sodium Azide

    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

    4 °C

    Expiry Date

    12 months
  • Target

    BIN1 (Bridging Integrator 1 (BIN1))

    Alternative Name

    Bin1

    Background

    Background: Bin1 (bridging integrator 1) may be involved in the regulation of synaptic vesicle endocytosis. It may act as a tumor suppressor and inhibits malignant cell transformation. Defects in BIN1 are the cause of centronuclear myopathy autosomal recessive (ARCNM) [taken from the Universal Protein Resource (UniProt) ww.uniprot.org/uniprot/O00499].

    Gene ID

    274

    NCBI Accession

    NP_647593

    UniProt

    O00499
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