C1ORF50 Antikörper (AA 111-199) (FITC)

Produktnummer ABIN1710785

Produktdetails anti-C1ORF50 Antikörper (FITC)

Target: C1ORF50 (Chromosome 1 Open Reading Frame 50 (C1ORF50))

Bindungsspezifität: AA 111-199

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser C1ORF50 Antikörper ist konjugiert mit FITC

Applikation: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Homologie: Human,Rat,Rabbit

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C1orf50

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Konservierungsmittel: ProClin

Vorsichtsmaßnahmen: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Haltbarkeit: 12 months

Details zu C1ORF50

Target: C1ORF50 (Chromosome 1 Open Reading Frame 50 (C1ORF50))

Andere Bezeichnung: C1orf50 (C1ORF50 Produkte)

Synonyme: c1orf50 antikoerper, chromosome 1 open reading frame 50 antikoerper, zgc:112255 antikoerper, chromosome 1 open reading frame 50 L homeolog antikoerper, C1orf50 antikoerper, zgc:112255 antikoerper, c1orf50.L antikoerper

Hintergrund:

Synonyms: C1orf50, CA050_HUMAN, Chromosome 1 open reading frame 50, MGC955, Uncharacterized protein C1orf50.

Background: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf50 gene product has been provisionally designated C1orf50 pending further characterization.

Gen-ID: 79078

Pathways: SARS-CoV-2 Protein Interaktom