HMX2 antibody

Catalog No. ABIN7228944

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

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: HMX2 Polyclonal Antibody

Specificity: The antibody detects endogenous levels of HMX2 protein

Purification: The antibody was affinity-purified from rabbit serum by affinity-chromatography using 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 (1:500-1:2000), ELISA (1:5000-1:20000).

Comment:

Primary Antibody

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

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: 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.

Target Details for HMX2

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

Alternative Name: HMX2

Background: Rabbit Anti-HMX2 Polyclonal Antibody,Homeobox protein HMX2, Homeobox protein H6 family member 2,The 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.,HMX2

Molecular Weight: observerd band 30kDa

Gene ID: 3167

UniProt: A2RU54