NBPF10 Antikörper (C-Term)

Produktnummer ABIN2790662

Der Kaninchen Polyklonal Anti-NBPF10-Antikörper wurde für WB validiert. Er ist geeignet, NBPF10 in Proben von Human zu detektieren.

Kurzübersicht für NBPF10 Antikörper (C-Term) (ABIN2790662)

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

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser NBPF10 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktdetails anti-NBPF10 Antikörper

Bindungsspezifität: C-Term

Sequenz: VLQDSLDRCY STPSS
CLEQPDSCQP YGSSFYALEE KHVGFSLDVG EIEK

Homologie: Human: 100%

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

Aufreinigung: Affinity Purified

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

Anwendungsinformationen

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

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

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Handhabung: Avoid repeat freeze-thaw cycles.

Lagerung: -20 °C

Informationen zur Lagerung: 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.

Details zu NBPF10

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

Andere Bezeichnung: NBPF10

Hintergrund: 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

Molekulargewicht: 84 kDa

Gen-ID: 55672

NCBI Accession: NM_017940, NP_060410

UniProt: Q3BBV0