C1orf144 Antikörper

Produktnummer ABIN1387177

Produktdetails anti-C1orf144 Antikörper

Target: C1orf144 (Chromosome 1 Open Reading Frame 144 (C1orf144))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser C1orf144 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Kreuzreaktivität: Human, Maus, Ratte

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C1orf144

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:300-5000
IHC-P 1:200-400
IF(IHC-P) 1:50-200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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: 4 °C,-20 °C

Informationen zur Lagerung: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Haltbarkeit: 12 months

Details zu C1orf144

Target: C1orf144 (Chromosome 1 Open Reading Frame 144 (C1orf144))

Andere Bezeichnung: C1orf144 (C1orf144 Produkte)

Synonyme: MGC82291 antikoerper, MGC76116 antikoerper, DKFZp468H135 antikoerper, C1orf144 antikoerper, SZRD1 antikoerper, 1110022I03 antikoerper, D4Ertd22e antikoerper, C2H1orf144 antikoerper, wu:fb15h05 antikoerper, wu:fk86c07 antikoerper, zgc:109926 antikoerper, RGD1560286 antikoerper, SUZ RNA binding domain containing 1 L homeolog antikoerper, SUZ RNA binding domain containing 1 antikoerper, szrd1.L antikoerper, szrd1 antikoerper, SZRD1 antikoerper, Szrd1 antikoerper

Hintergrund:

Synonyms: DKFZp566C0424, MGC70432, Putative MAPK-activating protein PM18/PM20/PM22, UPF0485 protein C1orf144, SZRD1_HUMAN, SUZ domain-containing protein 1.

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 C1orf144 gene product has been provisionally designated C1orf144 pending further characterization.

Gen-ID: 26099