NBPF3 Antikörper (N-Term)

Produktnummer ABIN5517639

Dieser Kaninchen Polyklonal Antikörper detektiert spezifisch NBPF3 in WB. Es zeigt Reaktivität gegenüber Proben von Human.

Kurzübersicht für NBPF3 Antikörper (N-Term) (ABIN5517639)

Target: NBPF3 (Neuroblastoma Breakpoint Family, Member 3 (NBPF3))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser NBPF3 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktdetails anti-NBPF3 Antikörper

Bindungsspezifität: N-Term

Sequenz: CDQVKKEDQE ATSPRLSREL LDEKEPEVLQ DSLDRFYSTP FEYLELPDLC

Homologie: Human: 100%

Produktmerkmale: This is a rabbit polyclonal antibody against NBPF3. It was validated on Western Blot.

Aufreinigung: Affinity Purified

Immunogen: The immunogen is a synthetic peptide directed towards the N-terminal region of Human NBPF3

Anwendungsinformationen

Applikationshinweise: Optimal working dilution should be determined by the investigator.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

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.

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 NBPF3

Target: NBPF3 (Neuroblastoma Breakpoint Family, Member 3 (NBPF3))

Andere Bezeichnung: NBPF3

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. DUF1220 copy number variations in 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: NBPF3, L7,

Protein Interaction Partner: NBPF3, APP, UBD, UBC, TSEN15, ANK1, EWSR1,

Protein Size: 275

Gen-ID: 84224