C9orf64 Antikörper (AA 161-260) (Biotin)

Produktnummer ABIN1701204

Produktdetails anti-C9orf64 Antikörper (Biotin)

Target: C9orf64 (Chromosome 9 Open Reading Frame 64 (C9orf64))

Bindungsspezifität: AA 161-260

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser C9orf64 Antikörper ist konjugiert mit Biotin

Applikation: Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Kreuzreaktivität: Human

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

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C9orf64

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

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 for 12 months.

Haltbarkeit: 12 months

Details zu C9orf64

Target: C9orf64 (Chromosome 9 Open Reading Frame 64 (C9orf64))

Andere Bezeichnung: C9orf64 (C9orf64 Produkte)

Synonyme: C9orf64 antikoerper, MGC84745 antikoerper, MGC97544 antikoerper, chromosome Z C9orf64 homolog antikoerper, chromosome 9 open reading frame 64 L homeolog antikoerper, chromosome 9 open reading frame 64 antikoerper, chromosome 15 open reading frame, human C9orf64 antikoerper, queuosine salvage protein antikoerper, CZH9orf64 antikoerper, c9orf64.L antikoerper, c9orf64 antikoerper, C15H9orf64 antikoerper, C8H9orf64 antikoerper, C9orf64 antikoerper

Hintergrund:

Synonyms: C9orf64, CI064_HUMAN, UPF0553 protein C9orf64.

Background: Chromosome 9 consists of about 145 million bases and 4 % of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The C9orf64 gene product has been provisionally designated C9orf64 pending further characterization.

Gen-ID: 84267