ELMOD3 antibody

Catalog No. ABIN6571201

This Rabbit Polyclonal antibody specifically detects ELMOD3 in WB. It exhibits reactivity toward Human, Mouse and Rat.

Quick Overview for ELMOD3 antibody (ABIN6571201)

Target: ELMOD3 (ELMO/CED-12 Domain Containing 3 (ELMOD3))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This ELMOD3 antibody is un-conjugated

Application: Western Blotting (WB)

Product Details anti-ELMOD3 Antibody

Purification: Affinity purification

Immunogen: Recombinant protein of human ELMOD3

Isotype: IgG

Application Details

Application Notes: WB 1:500 - 1:2000

Restrictions: For Research Use only

Handling

Concentration: 1 mg/mL

Buffer: Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.

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: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for ELMOD3

Target: ELMOD3 (ELMO/CED-12 Domain Containing 3 (ELMOD3))

Alternative Name: ELMOD3

Background:

Synonyms: ELMO Domain Containing 3,RNA-Binding Motif And ELMO Domain-Containing Protein 1,RNA Binding Motif And ELMO/CED-12 Domain 1,Deafness, Autosomal Recessive 88,ELMO/CED-12 Domain Containing 3,RNA-Binding Motif Protein 29,RBED1,RBM29,Liver-Specific Organic Anion Transporter 3TM12,ELMO Domain-Containing Protein 3,Organic Anion Transporter LST-3b,RNA Binding Motif Protein 29,RNA-Binding Protein 29,DFNB88,LST3

Background: This gene encodes a member of the engulfment and cell motility family of GTPase-activating proteins that regulate Arf GTPase proteins. Members of this family are defined by a conserved engulfment and cell motility domain. In rat cochlea, the encoded protein is found in stereocilia, kinocilia and cuticular plate of developing hair cells suggesting a function for this protein in cochlear sensory cells. An allelic variant of this family has been associated with autosomal recessive nonsyndromic deafness-88 in humans. Alternative splicing results in multiple transcript variants.

Molecular Weight:

Observed_MW: 38/43kDa

Calculated_MW: 18kDa/20kDa/28kDa/43kDa/44kDa

Gene ID: 84173

UniProt: Q96FG2