NBPF15 Antikörper (N-Term)

Produktnummer ABIN2791696

Der Kaninchen Polyklonal Anti-NBPF15-Antikörper wurde für WB validiert. Er ist geeignet, NBPF15 in Proben von Human zu detektieren.

Kurzübersicht für NBPF15 Antikörper (N-Term) (ABIN2791696)

Target: NBPF15 (Neuroblastoma Breakpoint Family, Member 15 (NBPF15))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser NBPF15 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktdetails anti-NBPF15 Antikörper

Bindungsspezifität: N-Term

Sequenz: VQKLSPENDN DDDEDVQVEV AEKVQKSSAP REMQKAEEKE VPEDSLEECA

Homologie: Human: 100%

Produktmerkmale: This is a rabbit polyclonal antibody against NBPF16. It was validated on Western Blot.

Aufreinigung: Affinity Purified

Immunogen: The immunogen is a synthetic peptide directed towards the N-terminal region of human NBPF15

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 NBPF15

Target: NBPF15 (Neuroblastoma Breakpoint Family, Member 15 (NBPF15))

Andere Bezeichnung: NBPF16

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: AG3, AB14, NBPF16
Protein Size: 670

Molekulargewicht: 73 kDa

Gen-ID: 284565

NCBI Accession: NM_001170755, NP_001164226

UniProt: Q5SXJ2