NBPF1 anticorps (C-Term)

N° du produit ABIN2790662

L’anticorps anti-NBPF1 Polyclonal Lapin est utilisé pour la détection de NBPF1 dans des échantillons de Humain. Il a été validé pour WB.

Aperçu rapide pour NBPF1 anticorps (C-Term) (ABIN2790662)

Antigène: NBPF1 (Neuroblastoma Breakpoint Family, Member 1 (NBPF1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp NBPF1 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-NBPF1 anticorps

Épitope: C-Term

Fonction: NBPF1 Antibody - C-terminal region

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

Indications d'application: Optimal working dilution should be determined by the investigator.

Commentaires:

We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP67194-100UG

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: 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: prevent freeze-thaw cycles

Stock: 4 °C,-20 °C

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

Détails sur NBPF1

Antigène: NBPF1 (Neuroblastoma Breakpoint Family, Member 1 (NBPF1))

Autre désignation: NBPF1

Sujet:

Background Information: 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.

Gene Name: neuroblastoma breakpoint family member 1

Alternative Symbols: AD2, NBG, AB13, AB14, AB23, NBPF

Protein Name: neuroblastoma breakpoint family member 1

Poids moléculaire: 84kDa

ID gène: 55672

NCBI Accession: NP_060410

UniProt: Q3BBV0