Msx2/Hox8 antibody (AA 1-129) (HRP)

Catalog No. ABIN8011758

The Rabbit Polyclonal anti-Msx2/Hox8 antibody is suitable to detect Msx2/Hox8 in samples from Human. It has been validated for WB, ELISA and IHC.

Quick Overview for Msx2/Hox8 antibody (AA 1-129) (HRP) (ABIN8011758)

Target: Msx2/Hox8 (Msx2) (Msh Momeobox 2 (Msx2))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Msx2/Hox8 antibody is conjugated to HRP

Application: Western Blotting (WB), ELISA, Immunohistochemistry (IHC)

Product Details anti-Msx2/Hox8 Antibody (HRP)

Binding Specificity: AA 1-129

Purpose: Anti-Hox8/MSX2 Antibody HRP Conjugated

Cross-Reactivity (Details): No cross-reactivity with other proteins.

Purification: Immunogen affinity purified.

Immunogen: E.coli-derived human Hox8/MSX2 recombinant protein (Position: M1-M129).

Isotype: IgG

Application Details

Application Notes: Western blot, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4.

Storage: -20 °C

Storage Comment: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing.

Expiry Date: 12 months

Target Details for Msx2/Hox8

Target: Msx2/Hox8 (Msx2) (Msh Momeobox 2 (Msx2))

Alternative Name: MSX2

Background:

Background: Homeobox protein MSX-2 is a protein that in humans is encoded by the MSX2 gene. This gene encodes a member of the muscle segment homeobox gene family. The encoded protein is a transcriptional repressor whose normal activity may establish a balance between survival and apoptosis of neural crest-derived cells required for proper craniofacial morphogenesis. The encoded protein may also have a role in promoting cell growth under certain conditions and may be an important target for the RAS signaling pathways. Mutations in this gene are associated with parietal foramina 1 and craniosynostosis type 2.

Gene Full Name: msh homeobox 2

Gene ID: 4488

UniProt: P35548