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ITGA7 antibody

The Rabbit Polyclonal anti-ITGA7 antibody is suitable to detect ITGA7 in samples from Human, Mouse and Rat. It has been validated for ELISA and IHC.
Catalog No. ABIN7244507
-15% Promotion 2026
$457.98
$538.80
save $80.82 (-15 %)
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Quick Overview for ITGA7 antibody (ABIN7244507)

Target

See all ITGA7 Antibodies
ITGA7 (Integrin, alpha 7 (ITGA7))

Reactivity

  • 45
  • 18
  • 5
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 37
  • 12
  • 1
Rabbit

Clonality

  • 38
  • 12
Polyclonal

Conjugate

  • 27
  • 4
  • 4
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This ITGA7 antibody is un-conjugated

Application

  • 33
  • 21
  • 10
  • 6
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
ELISA, Immunohistochemistry (IHC)
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Synthetic peptide of human ITGA7

    Isotype

    IgG
  • Application Notes

    IHC 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.7 mg/mL

    Buffer

    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

    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

    ITGA7 (Integrin, alpha 7 (ITGA7))

    Alternative Name

    ITGA7

    Background

    The protein encoded by this gene belongs to the integrin alpha chain family. Integrins are heterodimeric integral membrane proteins composed of an alpha chain and a beta chain. They mediate a wide spectrum of cell-cell and cell-matrix interactions, and thus play a role in cell migration, morphologic development, differentiation, and metastasis. This protein functions as a receptor for the basement membrane protein laminin-1. It is mainly expressed in skeletal and cardiac muscles and may be involved in differentiation and migration processes during myogenesis. Defects in this gene are associated with congenital myopathy. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.

    NCBI Accession

    NP_002197

    UniProt

    Q13683

    Pathways

    Integrin Complex
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