C9orf25 Antikörper (AA 1-100) (Biotin)

Produktnummer ABIN1700465

Produktdetails anti-C9orf25 Antikörper (Biotin)

Target: C9orf25 (Chromosome 9 Open Reading Frame 25 (C9orf25))

Bindungsspezifität: AA 1-100

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser C9orf25 Antikörper ist konjugiert mit Biotin

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

Homologie: Human,Mouse,Rat,Sheep,Horse,Chicken

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C9orf25

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 C9orf25

Target: C9orf25 (Chromosome 9 Open Reading Frame 25 (C9orf25))

Andere Bezeichnung: C9orf25 (C9orf25 Produkte)

Synonyme: C9orf25 antikoerper, bA573M23.5 antikoerper, C15H9orf25 antikoerper, 2310028H24Rik antikoerper, fam219a antikoerper, zgc:101028 antikoerper, family with sequence similarity 219 member A antikoerper, family with sequence similarity 219, member A antikoerper, family with sequence similarity 219, member Aa antikoerper, FAM219A antikoerper, Fam219a antikoerper, fam219aa antikoerper

Hintergrund:

Synonyms: bA573M23.5, C9orf25, Chromosome 9 open reading frame 25, F219A_HUMAN, FLJ39031, Hypothetical protein LOC203259, Uncharacterized protein C9orf25.

Background: C9orf25 (chromosome 9 open reading frame 25) is a 185 amino acid protein that exists as seven alternatively spliced isoforms that are encoded by a gene located on human chromosome 9. Chromosome 9 consists of about 145 million bases, represents 4 % of the human genome and encodes nearly 900 genes. Thought 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.

Gen-ID: 203259