TSACC/C1orf182 Antikörper (AA 21-100) (Alexa Fluor 350)

Produktnummer ABIN1692617

Produktdetails anti-TSACC/C1orf182 Antikörper (Alexa Fluor 350)

Target: TSACC/C1orf182 (TSACC) (TSSK6 Activating Co-Chaperone (TSACC))

Bindungsspezifität: AA 21-100

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser TSACC/C1orf182 Antikörper ist konjugiert mit Alexa Fluor 350

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

Homologie: Human

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C1orf182

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 TSACC/C1orf182

Target: TSACC/C1orf182 (TSACC) (TSSK6 Activating Co-Chaperone (TSACC))

Andere Bezeichnung: C1orf182 (TSACC Produkte)

Synonyme: SIP antikoerper, TP53DINP1 antikoerper, TP53INP1A antikoerper, TP53INP1B antikoerper, Teap antikoerper, p53DINP1 antikoerper, C1orf182 antikoerper, RP11-443G18.5 antikoerper, SSTK-IP antikoerper, 1700021C14Rik antikoerper, C3H1orf182 antikoerper, RGD1304953 antikoerper, tumor protein p53 inducible nuclear protein 1 antikoerper, TSSK6 activating cochaperone antikoerper, TSSK6 activating co-chaperone antikoerper, TP53INP1 antikoerper, TSACC antikoerper, Tsacc antikoerper

Hintergrund:

Synonyms: C1orf182, CA182_HUMAN, SSTK-interacting protein, SSTK-IP, Uncharacterized protein C1orf182.

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 C1orf182 gene product has been provisionally designated C1orf182 pending further characterization.

Gen-ID: 128229