CECR5 antibody

Catalog No. ABIN7244657

This anti-CECR5 antibody is a Rabbit Polyclonal antibody detecting CECR5 in WB and ELISA. Suitable for Human.

Quick Overview for CECR5 antibody (ABIN7244657)

Target: CECR5 (Cat Eye Syndrome Chromosome Region, Candidate 5 (CECR5))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CECR5 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-CECR5 Antibody

Characteristics: Polyclonal Antibody

Purification: Antigen affinity purification

Immunogen: Synthetic peptide of human CECR5

Isotype: IgG

Application Details

Application Notes: WB 1:500-1:2000, ELISA 1:5000-1:10000

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1.3 mg/mL

Buffer: PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

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 CECR5

Target: CECR5 (Cat Eye Syndrome Chromosome Region, Candidate 5 (CECR5))

Alternative Name: CECR5

Background: Adenosine deaminase is an enzyme that is present in most tissues and exists predominantly as a monomer, although in some tissues it is associated with adenosine deaminase-binding protein. Adenosine deaminase degrades extracellular adenosine, which is toxic for lymphocytes. A novel family of growth factors that share sequence similarity to adenosine deaminase has been identified. The cat eye syndrome critical region protein (CECR) family includes CECR1, CECR2, CECR3, CECR4, CECR5, CECR6, CECR7, CECR8 and CECR9. The genes encoding CECR proteins are candidates for Cat Eye Syndrome (CES), a developmental disorder associated with the duplication of a 2 Mb region of 22q11.2. CES is characterized by the combination of coloboma of the iris and anal atresia with fistula, downslanting palpebral fissures, preauricular tags and/or pits, frequent occurrence of heart and renal malformations, and normal or near-normal mental development. CECR family members are widely expressed. Specifically, CECR1 has the highest expression in adult heart, lung, lymphoblasts and placenta. CECR2 is also involved in neurulation and chromatin remodeling. Mutations in the CECR2 gene result in neural tube defects.

Molecular Weight:

Observed_MW: Refer to figures

Calculated_MW: 46 kDa

UniProt: Q9BXW7