Msx2/Hox8 antibody (AA 1-129) (Fluoro594)

Catalog No. ABIN8011756

The Fluoro594-conjugated Rabbit Polyclonal anti-Msx2/Hox8 antibody (ABIN8011756) specifically detects Msx2/Hox8 in FACS. The antibody is reactive with Human samples.

Quick Overview for Msx2/Hox8 antibody (AA 1-129) (Fluoro594) (ABIN8011756)

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

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Msx2/Hox8 antibody is conjugated to Fluoro594

Application: Flow Cytometry (FACS)

Product Details anti-Msx2/Hox8 Antibody (Fluoro594)

Binding Specificity: AA 1-129

Purpose: Anti-Hox8/MSX2 Antibody Fluoro594 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: Flow Cytometry, 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, 0.02 % 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: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

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