DPPA4 antibody (AA 51-150) (Biotin)

Catalog No. ABIN1700266

This Rabbit Polyclonal antibody specifically detects DPPA4 in ELISA, IHC (p), IHC (fro). It exhibits reactivity toward Human.

Quick Overview for DPPA4 antibody (AA 51-150) (Biotin) (ABIN1700266)

Target: DPPA4 (Developmental Pluripotency Associated 4 (DPPA4))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This DPPA4 antibody is conjugated to Biotin

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

Product Details anti-DPPA4 Antibody (Biotin)

Binding Specificity: AA 51-150

Predicted Reactivity: Human,Mouse,Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human Dppa4

Isotype: IgG

Application Details

Application Notes: 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 DPPA4

Target: DPPA4 (Developmental Pluripotency Associated 4 (DPPA4))

Alternative Name: Dppa4

Background:

Synonyms: 2410091M23Rik, Developmental pluripotency associated 4, Developmental pluripotency associated protein 4, Developmental pluripotency-associated protein 4, Dppa 4, DPPA4, DPPA4_HUMAN, FLJ10713.

Background: DPPA4 (developmental pluripotency associated 4) is a 304 amino acid protein that localizes to the nucleus and is thought to be involved in the maintenance of cell pluripotentiality during embryogenesis. The gene encoding DPPA4 maps to human chromosome 3, which houses over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci. Key tumor suppressing genes on chromosome 3 include those that encode the apoptosis mediator RASSF1, the cell migration regulator HYAL1 and the angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.