NBPF7 Antikörper (AA 361-410)
Kurzübersicht für NBPF7 Antikörper (AA 361-410) (ABIN1535096)
Target
Reaktivität
Wirt
Klonalität
Konjugat
Applikation
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Bindungsspezifität
- AA 361-410
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Verwendungszweck
- NBPF7 Antibody
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Spezifität
- NBPF7 Polyclonal Antibody detects endogenous levels of NBPF7 protein.
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Aufreinigung
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
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Reinheit
- > 95 %
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Immunogen
- The antiserum was produced against synthesized peptide derived from human NBPF7. AA range:361-410
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Isotyp
- IgG
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Applikationshinweise
- WB 1:500-2000,IHC 1:50-300
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Beschränkungen
- Nur für Forschungszwecke einsetzbar
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Format
- Liquid
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Konzentration
- 1 mg/mL
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Buffer
- Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.
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Konservierungsmittel
- Sodium azide
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Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Lagerung
- -20 °C
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Informationen zur Lagerung
- Store at -20°C/1 year
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Haltbarkeit
- 12 months
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- NBPF7 (Neuroblastoma Breakpoint Family, Member 7 (NBPF7))
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Andere Bezeichnung
- NBPF7
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Hintergrund
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Synonyms: NBPF7, Putative neuroblastoma breakpoint family member 7
Background: neuroblastoma breakpoint family member 7(NBPF7) Homo sapiens 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 fam
Gene Name: NBPF7
Protein Name: Putative neuroblastoma breakpoint family member 7
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Molekulargewicht
- 48 kDa
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Gen-ID
- 343505
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UniProt
- P0C2Y1
Target
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