C11orf65 Antikörper (Alexa Fluor 555)

Produktnummer ABIN1405565

Produktdetails anti-C11orf65 Antikörper (Alexa Fluor 555)

Target: C11orf65 (Chromosome 11 Open Reading Frame 65 (C11orf65))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser C11orf65 Antikörper ist konjugiert mit Alexa Fluor 555

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

Kreuzreaktivität: Human, Maus, Ratte

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C11orf65

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IF(IHC-P) 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 C11orf65

Target: C11orf65 (Chromosome 11 Open Reading Frame 65 (C11orf65))

Andere Bezeichnung: C11orf65 (C11orf65 Produkte)

Synonyme: AU017961 antikoerper, chromosome 11 open reading frame 65 antikoerper, chromosome 11 open reading frame 65 L homeolog antikoerper, chromosome 14 open reading frame, human C11orf65 antikoerper, RIKEN cDNA 4930550C14 gene antikoerper, similar to RIKEN cDNA 4930550C14 antikoerper, C11orf65 antikoerper, c11orf65.L antikoerper, C14H11orf65 antikoerper, 4930550C14Rik antikoerper, RGD1311251 antikoerper

Hintergrund:

Synonyms: Chromosome 11 open reading frame 65, Hypothetical protein LOC160140, CK065_HUMAN.

Background: C11orf65, also known as MGC33948, is a 313 amino acid protein that is encoded by a gene located on human chromosome 11. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4 % of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and _ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.

Gen-ID: 160140