C9ORF91 Antikörper (AA 151-250) (Biotin)

Produktnummer ABIN1700232

Dieses Anti-C9ORF91-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von C9ORF91 in WB, ELISA, IHC (p) und IHC (fro). Geeignet für Human.

Kurzübersicht für C9ORF91 Antikörper (AA 151-250) (Biotin) (ABIN1700232)

Target: C9ORF91 (Chromosome 9 Open Reading Frame 91 (C9ORF91))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser C9ORF91 Antikörper ist konjugiert mit Biotin

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

Produktdetails anti-C9ORF91 Antikörper (Biotin)

Bindungsspezifität: AA 151-250

Homologie: Human,Mouse,Rat

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C9ORF91

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 C9ORF91

Target: C9ORF91 (Chromosome 9 Open Reading Frame 91 (C9ORF91))

Andere Bezeichnung: C9ORF91

Hintergrund:

Synonyms: C9orf91, Chromosome 9 open reading frame 91, CI091_HUMAN, RP11-402G3.2, Transmembrane protein C9orf91.

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 C9orf91 gene product has been provisionally designated C9orf91 pending further characterization. There are three isoforms of C9orf91 that are produced as a result of alternative splicing events.

Gen-ID: 203197