C15orf40 Antikörper

Produktnummer ABIN7246064

Produktdetails anti-C15orf40 Antikörper

Target: C15orf40 (Chromosome 15 Open Reading Frame 40 (C15orf40))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser C15orf40 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA, Immunohistochemistry (IHC)

Produktmerkmale: Polyclonal Antibody

Aufreinigung: Antigen affinity purification

Immunogen: Fusion protein of human C15orf40

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:500-1:2000, IHC 1:25-1:100, ELISA 1:5000-1:10000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.5 mg/mL

Buffer: PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

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: Store at -20°C. Avoid freeze / thaw cycles.

Details zu C15orf40

Target: C15orf40 (Chromosome 15 Open Reading Frame 40 (C15orf40))

Andere Bezeichnung: C15orf40 (C15orf40 Produkte)

Synonyme: MGC89060 antikoerper, AI851475 antikoerper, C15orf40 antikoerper, c15orf40 antikoerper, chromosome 15 open reading frame 40 antikoerper, RIKEN cDNA 3110040N11 gene antikoerper, similar to RIKEN cDNA 3110040N11 antikoerper, chromosome 21 open reading frame, human C15orf40 antikoerper, chromosome 15 open reading frame 40 L homeolog antikoerper, C15orf40 antikoerper, c15orf40 antikoerper, 3110040N11Rik antikoerper, RGD1305713 antikoerper, C21H15orf40 antikoerper, c15orf40.L antikoerper

Hintergrund: Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3 % of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The C15orf40 gene product has been provisionally designated C15orf40 pending further characterization.

Molekulargewicht:

Observed_MW: Refer to figures

Calculated_MW: 16 kDa

UniProt: Q8WUR7