CPXCR1 antibody (AA 151-250) (Biotin)

Catalog No. ABIN1398463

Product Details anti-CPXCR1 Antibody (Biotin)

Target: CPXCR1 (CPX Chromosome Region, Candidate 1 (CPXCR1))

Binding Specificity: AA 151-250

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CPXCR1 antibody is conjugated to Biotin

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Predicted Reactivity: Human,Horse

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human CPXCR1

Isotype: IgG

Application Details

Application Notes: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

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: Store at -20°C for 12 months.

Expiry Date: 12 months

Target Details for CPXCR1

Target: CPXCR1 (CPX Chromosome Region, Candidate 1 (CPXCR1))

Alternative Name: CPXCR1 (CPXCR1 Products)

Synonyms: CT77 antibody, Gm1143 antibody, CPX chromosome region, candidate 1 antibody, CPXCR1 antibody, Cpxcr1 antibody

Background:

Synonyms: Cancer/testis antigen 77, CPX chromosome region, candidate 1, CPX candidate region 1 protein, CPX chromosomal region candidate gene 1 protein, CPX chromosomal region candidate gene 1 protein homolog, CPX chromosome region, candidate 1, CT77, Gm1143, CPXCR_HUMAN.

Background: CPXCR1 is widely expressed in fetal tissues, including the tongue, mandible and palate with an unknown function. Cleft palate most commonly occurs as a sporadic multifactorial disorder with a clear but difficult to define genetic component. As a semi-dominant disorder, X-linked cleft palate (CPX) provides a useful model to investigate a congenital defect that is little influenced by non-genetic factors.

Gene ID: 53336