NBPF6 anticorps (N-Term)

N° du produit ABIN2791691

L’anticorps Lapin Polyclonal anti-NBPF6 a été validé pour WB. Il convient pour détecter NBPF6 dans des échantillons de Humain.

Aperçu rapide pour NBPF6 anticorps (N-Term) (ABIN2791691)

Antigène: NBPF6 (Neuroblastoma Breakpoint Family, Member 6 (NBPF6))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp NBPF6 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-NBPF6 anticorps

Épitope: N-Term

Séquence: EKVQESPAPR EVQKTEEKEV PQDSLEECAV TCSNSHNPSN SNQPHRSTKI

Homologie: Human: 100%

Attributs du produit: This is a rabbit polyclonal antibody against NBPF6. It was validated on Western Blot.

Purification: Affinity Purified

Immunogène: The immunogen is a synthetic peptide directed towards the N-terminal region of Human NBPF6

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 NBPF6

Antigène: NBPF6 (Neuroblastoma Breakpoint Family, Member 6 (NBPF6))

Autre désignation: NBPF6

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.
Alias Symbols: -
Protein Size: 638

Poids moléculaire: 70 kDa

ID gène: 653149

NCBI Accession: NM_001143988, NP_001137460

UniProt: Q5VWK0