Msx2/Hox8 antibody (AA 120-148)

Catalog No. ABIN5534538

Product Details anti-Msx2/Hox8 Antibody

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

Binding Specificity: AA 120-148

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Msx2/Hox8 antibody is un-conjugated

Application: Western Blotting (WB)

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This MSX2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 120-148 amino acids from the Central region of human MSX2.

Isotype: Ig Fraction

Application Details

Application Notes: For WB starting dilution is: 1:1000

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: Supplied in PBS with 0.09 % (W/V) 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: 4 °C,-20 °C

Storage Comment: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Target Details for Msx2/Hox8

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

Alternative Name: MSX2 (Msx2 Products)

Synonyms: CRS2 antibody, FPP antibody, HOX8 antibody, MSH antibody, PFM antibody, PFM1 antibody, BB122635 antibody, Hox-8 antibody, Hox8 antibody, Hox8.1 antibody, HOX-8 antibody, Msx-2 antibody, msh homeobox 2 antibody, MSX2 antibody, Msx2 antibody

Background: 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.

Molecular Weight: 29 kDa

Gene ID: 4488

UniProt: P35548