DPPA5 anticorps (AA 1-100) (Cy7)

N° du produit ABIN1413588

Cet anticorps anti-DPPA5 est un anticorps Lapin Polyclonal détectant DPPA5 dans IF (cc) et IF (p). Adapté pour Humain.

Aperçu rapide pour DPPA5 anticorps (AA 1-100) (Cy7) (ABIN1413588)

Antigène: DPPA5 (Developmental Pluripotency Associated 5 (DPPA5))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp DPPA5 est conjugé à/à la Cy7

Application: Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Détail du produit anti-DPPA5 anticorps (Cy7)

Épitope: AA 1-100

Homologie: Human,Mouse,Rat,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human DPPA5

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Stockage

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.

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur DPPA5

Antigène: DPPA5 (Developmental Pluripotency Associated 5 (DPPA5))

Autre désignation: DPPA5

Sujet:

Synonyms: Developmental pluripotency associated 5, DPPA5, Embryonal stem cell specic gene 1 protein, Esg 1, ESG1, hDPPA5, DPPA5_HUMAN.

Background: DPPA5 is a 116 amino acid protein that localizes to the cytoplasm and contains one KH domain. Expressed in embryonic germ (EG), primordial germ (PG) and embryonic stem (ES) cells, DPPA5 plays an important role in the maintenance of ES cell pluripotency and may be necessary for proper embryogenesis. The gene encoding DPPA5 maps to human chromosome 6, which contains 170 million base pairs and comprises nearly 6 % of the human genome. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer, suggesting the presence of a cancer susceptibility locus. Additionally, Porphyria cutanea tarda, Parkinson's disease, Stickler syndrome and a susceptibility to bipolar disorder are all associated with genes that map to chromosome 6.

ID gène: 340168