Thermo Fisher Scientific ITGA7 Monoclonal Antibody (8G2)

Applications

Tested Dilution

Publications

Western Blot (WB)

1-5 µg/mL

-

ELISA (ELISA)

0.1 ng/mL

-

Product Specifications

Species Reactivity

Human

Host/Isotype

Mouse / IgG2a, kappa

Class

Monoclonal

Type

Antibody

Clone

8G2

Immunogen

ITGA7 (NP_002197, 478 a.a. approximately 577 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa. if (typeof window.$mangular === undefined || !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{targetFamily:ITGA7 (Integrin alpha 7),uniProtId:Q13683-1,ncbiNodeId:9606,antigenRange:478-577,antigenLength:1181,antigenImageFileName:H00003679-M01_ITGA7_Integrin_alpha_7_Q13683-1_House_mouse.svg,antigenImageFileNamePDP:H00003679-M01_ITGA7_Integrin_alpha_7_Q13683-1_House_mouse_PDP.jpeg,sortOrder:1}\]; $mangular.isB2BCMGT = false; $mangular.isEpitopesModalImageMultiSizeEnabled = true;

View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}

Conjugate

Unconjugated Unconjugated Unconjugated

Form

Liquid

Concentration

See Label

Purification

Affinity chromatography

Storage buffer

PBS, pH 7.4

Contains

no preservative

Storage conditions

-20° C, Avoid Freeze/Thaw Cycles

Shipping conditions

Ambient (domestic); Wet ice (international)

Product Specific Information

Sequence of this protein is as follows: SHEVSIAPRS IDLEQPNCAG GHSVCVDLRV CFSYIAVPSS YSPTVALDYV LDADTDRRLR GQVPRVTFLS RNLEEPKHQA SGTVWLKHQH DRVCGDAMFQ

Target Information

Integrin alpha-7 is a protein that in humans is encoded by the ITGA7 gene. This gene is mapped to 12q13.2. 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.

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.