CPXCR1 anticorps (AA 151-250)

N° du produit ABIN1385302

Cet anticorps Lapin Polyclonal détecte spécifiquement CPXCR1 dans WB, ELISA, IF (cc), IF (p), IHC (p) et IHC (fro). Il présente une réactivité envers Humain.

Aperçu rapide pour CPXCR1 anticorps (AA 151-250) (ABIN1385302)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CPXCR1 est non-conjugé

Application: Western Blotting (WB), ELISA, Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Détail du produit anti-CPXCR1 anticorps

Épitope: AA 151-250

Homologie: Human,Horse

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human CPXCR1

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
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: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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: 4 °C,-20 °C

Stockage commentaire: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Date de péremption: 12 months

Détails sur CPXCR1

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

Autre désignation: CPXCR1

Sujet:

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.

ID gène: 53336