NBPF7 anticorps (AA 361-410)

N° du produit ABIN1535096

Cet anticorps anti-NBPF7 Polyclonal Lapin (ABIN1535096) détecte spécifiquement NBPF7 dans WB et IHC. L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour NBPF7 anticorps (AA 361-410) (ABIN1535096)

Antigène: NBPF7 (Neuroblastoma Breakpoint Family, Member 7 (NBPF7))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp NBPF7 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC)

Détail du produit anti-NBPF7 anticorps

Épitope: AA 361-410

Fonction: NBPF7 Antibody

Specificité: NBPF7 Polyclonal Antibody detects endogenous levels of NBPF7 protein.

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Pureté: > 95 %

Immunogène: The antiserum was produced against synthesized peptide derived from human NBPF7. AA range:361-410

Isotype: IgG

Information d'application

Indications d'application: WB 1:500-2000,IHC 1:50-300

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.

Agent conservateur: Sodium azide

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

Stock: -20 °C

Stockage commentaire: Store at -20°C/1 year

Date de péremption: 12 months

Détails sur NBPF7

Antigène: NBPF7 (Neuroblastoma Breakpoint Family, Member 7 (NBPF7))

Autre désignation: NBPF7

Sujet:

Synonyms: NBPF7, Putative neuroblastoma breakpoint family member 7

Background: neuroblastoma breakpoint family member 7(NBPF7) Homo sapiens This gene is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1. This gene family has experienced its greatest expansion within the human lineage and has expanded, to a lesser extent, among primates in general. Members of this gene family are characterized by tandemly repeated copies of DUF1220 protein domains. Gene copy number variations in the human chromosomal region 1q21.1, where most DUF1220 domains are located, have been implicated in a number of developmental and neurogenetic diseases such as microcephaly, macrocephaly, autism, schizophrenia, mental retardation, congenital heart disease, neuroblastoma, and congenital kidney and urinary tract anomalies. Altered expression of some gene family members is associated with several types of cancer. This gene fam

Gene Name: NBPF7

Protein Name: Putative neuroblastoma breakpoint family member 7

Poids moléculaire: 48 kDa

ID gène: 343505

UniProt: P0C2Y1