HMX2 antibody

Catalog No. ABIN7228944

The Rabbit Polyclonal anti-HMX2 antibody is suitable to detect HMX2 in samples from Human and Mouse. It has been validated for WB and ELISA.

Quick Overview for HMX2 antibody (ABIN7228944)

Target: HMX2 (H6 Family Homeobox 2 (HMX2))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This HMX2 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-HMX2 Antibody

Purpose: Rabbit Anti-HMX2 Polyclonal Antibody

Specificity: The antibody detects endogenous levels of HMX2 protein

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogen: Synthesized peptide derived from part region of human HMX2 protein

Isotype: IgG

Application Details

Application Notes: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000,ELISA 1:5000-20000

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Expiry Date: 12 months

Target Details for HMX2

Target: HMX2 (H6 Family Homeobox 2 (HMX2))

Alternative Name: HMX2

Background: Homeobox protein HMX2, Homeobox protein H6 family member 2The protein encoded by HMX2 is a member of the NKL homeobox family of transcription factors. Members in this family are of ancient origin and play an important role in organ development during embryogenesis. A related mouse protein plays a role in patterning of inner ear structures. In humans, variations in a region containing HMX2 have been associated with inner ear malformations, vestibular dysfunction, and hearing loss. HMX2 (H6 Family Homeobox 2) is a Protein Coding gene. Diseases associated with HMX2 include Cecal Benign Neoplasm and Cecum Adenocarcinoma.

Molecular Weight: 30kD

Gene ID: 3167

UniProt: A2RU54