SAPCD2 Antikörper (AA 301-394) (Biotin)

Produktnummer ABIN1700490

Dieses Anti-SAPCD2-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von SAPCD2 in WB, ELISA, IHC (fro) und IHC (p). Geeignet für Ratte.

Kurzübersicht für SAPCD2 Antikörper (AA 301-394) (Biotin) (ABIN1700490)

Target: SAPCD2 (Suppressor APC Domain Containing 2 (SAPCD2))

Reaktivität: Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SAPCD2 Antikörper ist konjugiert mit Biotin

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

Produktdetails anti-SAPCD2 Antikörper (Biotin)

Bindungsspezifität: AA 301-394

Kreuzreaktivität: Ratte

Homologie: Human,Mouse,Cow,Horse,Chicken,Rabbit

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C9orf140

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 SAPCD2

Target: SAPCD2 (Suppressor APC Domain Containing 2 (SAPCD2))

Andere Bezeichnung: C9orf140

Hintergrund:

Synonyms: 2010317E24Rik, C9orf140, Chromosome 9 open reading frame 140, SAPC2_HUMAN, p42.3, Protein C9orf140, SAPCD2, Suppressor APC domain containing 2, Suppressor APC domain containing protein 2, TS/MDEP, Tumor specicity and mitosis phase-dependent expression protein.

Background: C9orf140 (chromosome 9 open reading frame 140), also known as TS/MDEP (tumor specificity and mitosis phase-dependent expression protein) or p42.3, is a 394 amino acid nuclear and cytoplasmic 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: 89958