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anti-NBPF10 Anticorps

NBPF10 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.

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anti-NBPF10 anticorps (Neuroblastoma Breakpoint Family, Member 10) (C-Term) Primary Antibody

NBPF10 Reactivité: Humain WB Hôte: Lapin Polyclonal unconjugated

Image no. 1 for anti-Neuroblastoma Breakpoint Family, Member 10 (NBPF10) (C-Term) antibody (ABIN2790662)

N° du produit ABIN2790662

$389.00

Plus shipping costs $45.00

100 μL

Destination: Etats-Unis

Envoi sous 2 à 3 jours ouvrables

Détails

anti-NBPF10 anticorps (Neuroblastoma Breakpoint Family, Member 10) (C-Term) Primary Antibody

NBPF10 Reactivité: Humain IP, WB Hôte: Lapin Polyclonal unconjugated

N° du produit ABIN2585662

$375.83

Plus shipping costs $45.00

100 μL

Destination: Etats-Unis

Envoi sous 11 à 14 jours ouvrables

Détails

anti-NBPF10 anticorps (Neuroblastoma Breakpoint Family, Member 10) (AA 656-705) Primary Antibody

NBPF10 Reactivité: Humain WB Hôte: Lapin Polyclonal unconjugated

N° du produit ABIN6752783

$551.83

Plus shipping costs $45.00

100 μL

Destination: Etats-Unis

Envoi sous 11 à 14 jours ouvrables

Détails

NBPF10 profil antigène

Profil protéine

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 family contains numerous pseudogenes.