NBPF6 Antikörper (N-Term)

Produktnummer ABIN2791691

Der Kaninchen Polyklonal Anti-NBPF6-Antikörper wurde für WB validiert. Er ist geeignet, NBPF6 in Proben von Human zu detektieren.

Kurzübersicht für NBPF6 Antikörper (N-Term) (ABIN2791691)

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

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser NBPF6 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktdetails anti-NBPF6 Antikörper

Bindungsspezifität: N-Term

Sequenz: EKVQESPAPR EVQKTEEKEV PQDSLEECAV TCSNSHNPSN SNQPHRSTKI

Homologie: Human: 100%

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

Aufreinigung: Affinity Purified

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

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 NBPF6

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

Andere Bezeichnung: NBPF6

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.
Alias Symbols: -
Protein Size: 638

Molekulargewicht: 70 kDa

Gen-ID: 653149

NCBI Accession: NM_001143988, NP_001137460

UniProt: Q5VWK0