NBPF4 anticorps (AA 48-97)

N° du produit ABIN1451391

Cet anticorps anti-NBPF4 Polyclonal Lapin (ABIN1451391) détecte spécifiquement NBPF4 dans IHC, ELISA et IF. L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour NBPF4 anticorps (AA 48-97) (ABIN1451391)

Antigène: NBPF4 (Neuroblastoma Breakpoint Family, Member 4 (NBPF4))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp NBPF4 est non-conjugé

Application: Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF)

Détail du produit anti-NBPF4 anticorps

Épitope: AA 48-97

Fonction: NBPF4 Antibody

Specificité: NBPF4 Polyclonal Antibody detects endogenous levels of NBPF4 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 NBPF4. AA range:48-97

Isotype: IgG

Information d'application

Indications d'application: IHC 1:100 - 1:300. ELISA: 1:40000.. IF 1:50-200

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 NBPF4

Antigène: NBPF4 (Neuroblastoma Breakpoint Family, Member 4 (NBPF4))

Autre désignation: NBPF4

Sujet:

Synonyms: NBPF4, Neuroblastoma breakpoint family member 4

Background: neuroblastoma breakpoint family member 4(NBPF4) 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: NBPF4

Protein Name: Neuroblastoma breakpoint family member 4

Poids moléculaire: 14 kDa

ID gène: 148545

UniProt: Q96M43