CTTNBP2NL Antikörper (AA 5-110) (Alexa Fluor 488)

Produktnummer ABIN6942710

Produktdetails anti-CTTNBP2NL Antikörper (Alexa Fluor 488)

Target: CTTNBP2NL (CTTNBP2 N-terminal Like (CTTNBP2NL))

Bindungsspezifität: AA 5-110

Reaktivität: Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser CTTNBP2NL Antikörper ist konjugiert mit Alexa Fluor 488

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

Kreuzreaktivität: Ratte

Homologie: Human,Mouse,Cow,Pig,Horse,Chicken,Rabbit

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human CTTNBP2NL

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 CTTNBP2NL

Target: CTTNBP2NL (CTTNBP2 N-terminal Like (CTTNBP2NL))

Andere Bezeichnung: CTTNBP2NL (CTTNBP2NL Produkte)

Synonyme: AA552995 antikoerper, AA589392 antikoerper, AU018624 antikoerper, BC003236 antikoerper, mKIAA1433 antikoerper, CTTNBP2 N-terminal like antikoerper, CTTNBP2NL antikoerper, Cttnbp2nl antikoerper

Hintergrund:

Synonyms: CT2NL_HUMAN, CTTNBP2 N terminal like, CTTNBP2 N terminal like protein, CTTNBP2 N-terminal-like protein, Cttnbp2nl, DKFZp547A023, FLJ13278, KIAA1433.

Background: CTTNBP2NL is a 639 amino acid protein that is encoded by a gene that maps to human chromosome 1p13.2. 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.

Gen-ID: 55917

UniProt: Q9P2B4