NBPF10 anticorps (C-Term)

N° du produit ABIN2790662

L’anticorps Lapin Polyclonal anti-NBPF10 a été validé pour WB. Il convient pour détecter NBPF10 dans des échantillons de Humain.

Aperçu rapide pour NBPF10 anticorps (C-Term) (ABIN2790662)

Antigène: NBPF10 (Neuroblastoma Breakpoint Family, Member 10 (NBPF10))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp NBPF10 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-NBPF10 anticorps

Épitope: C-Term

Séquence: VLQDSLDRCY STPSS
CLEQPDSCQP YGSSFYALEE KHVGFSLDVG EIEK

Homologie: Human: 100%

Attributs du produit: This is a rabbit polyclonal antibody against NBPF10. It was validated on Western Blot.

Purification: Affinity Purified

Immunogène: The immunogen is a synthetic peptide directed towards the C-terminal region of human NBPF1

Information d'application

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

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.

Conseil sur la manipulation: Avoid repeat freeze-thaw cycles.

Stock: -20 °C

Stockage commentaire: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Détails sur NBPF10

Antigène: NBPF10 (Neuroblastoma Breakpoint Family, Member 10 (NBPF10))

Autre désignation: NBPF10

Sujet: 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.
Alias Symbols: AD2, NBG, AB13, AB14, AB23, NBPF
Protein Size: 766

Poids moléculaire: 84 kDa

ID gène: 55672

NCBI Accession: NM_017940, NP_060410

UniProt: Q3BBV0