C9ORF139 Antikörper (AA 101-190) (Biotin)

Produktnummer ABIN1699944

Dieses Anti-C9ORF139-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von C9ORF139 in WB, ELISA, IHC (fro) und IHC (p). Geeignet für Human.

Kurzübersicht für C9ORF139 Antikörper (AA 101-190) (Biotin) (ABIN1699944)

Target: C9ORF139 (Chromosome 9 Open Reading Frame 139 (C9ORF139))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser C9ORF139 Antikörper ist konjugiert mit Biotin

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

Produktdetails anti-C9ORF139 Antikörper (Biotin)

Bindungsspezifität: AA 101-190

Homologie: Human

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C9orf139

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 C9ORF139

Target: C9ORF139 (Chromosome 9 Open Reading Frame 139 (C9ORF139))

Andere Bezeichnung: C9orf139

Hintergrund:

Synonyms: C9orf139, Chromosome 9 open reading frame 139, CI139_HUMAN, Uncharacterized protein C9orf139.

Background: C9orf139 (chromosome 9 open reading frame 139) is a 190 amino acid protein encoded by a gene that maps to human chromosome 9q34.3. 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: 401563