C1orf131 Antikörper (AA 121-220) (FITC)

Produktnummer ABIN1709822

Produktdetails anti-C1orf131 Antikörper (FITC)

Target: C1orf131 (Chromosome 1 Open Reading Frame 131 (C1orf131))

Bindungsspezifität: AA 121-220

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser C1orf131 Antikörper ist konjugiert mit FITC

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

Homologie: Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Horse,Chicken,Rabbit

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C1orf131

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 C1orf131

Target: C1orf131 (Chromosome 1 Open Reading Frame 131 (C1orf131))

Andere Bezeichnung: C1orf131 (C1orf131 Produkte)

Synonyme: C3H1orf131 antikoerper, 3110004G14Rik antikoerper, Ayu21-55 antikoerper, Gt(pU21)55Imeg antikoerper, GtAyu21-55 antikoerper, chromosome 1 open reading frame 131 antikoerper, chromosome 3 open reading frame, human C1orf131 antikoerper, RIKEN cDNA 2810004N23 gene antikoerper, similar to RIKEN cDNA 0610039J04 antikoerper, C1orf131 antikoerper, C3H1ORF131 antikoerper, c1orf131 antikoerper, 2810004N23Rik antikoerper, RGD1562218 antikoerper

Hintergrund:

Synonyms: C1orf131, CA131_HUMAN, Chromosome 1 open reading frame 131, DKFZp547B1713, Hypothetical protein LOC128061, OTTHUMP00000036145, OTTHUMP00000036146, RP4-609B14.1, Uncharacterized protein C1orf131.

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 C1orf131 gene product has been provisionally designated C1orf131 pending further characterization.

Gen-ID: 128061