ITGA7 antibody (AA 229-257)

Catalog No. ABIN3031400

The Rabbit Polyclonal anti-ITGA7 antibody is suitable to detect ITGA7 in samples from Human. It has been validated for WB and ELISA.

Quick Overview for ITGA7 antibody (AA 229-257) (ABIN3031400)

Target: ITGA7 (Integrin, alpha 7 (ITGA7))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This ITGA7 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-ITGA7 Antibody

Binding Specificity: AA 229-257

Purpose: Integrin alpha 7 Antibody

Cross-Reactivity (Details): Expected species reactivity: Mouse

Purification: Antigen affinity

Immunogen: A portion of amino acids 229-257 from the human protein was used as the immunogen for this Integrin alpha 7 antibody.

Isotype: Ig Fraction

Application Details

Application Notes: Titration of the Integrin alpha 7 antibody may be required due to differences in protocols and secondary/substrate sensitivity.

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: In 1X PBS, pH 7.4, with 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: -20 °C

Storage Comment: Aliquot the Integrin alpha 7 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.

Target Details for ITGA7

Target: ITGA7 (Integrin, alpha 7 (ITGA7))

Alternative Name: Integrin alpha 7

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.

UniProt: Q13683

Pathways: Integrin Complex