CACTIN Antikörper (Biotin)

Produktnummer ABIN1405687

Produktdetails anti-CACTIN Antikörper (Biotin)

Target: CACTIN (Cactin, Spliceosome C Complex Subunit (CACTIN))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser CACTIN Antikörper ist konjugiert mit Biotin

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

Kreuzreaktivität: Human, Maus, Ratte

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human Cactin/C19orf29

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:300-5000
IHC-P 1:200-400

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 CACTIN

Target: CACTIN (Cactin, Spliceosome C Complex Subunit (CACTIN))

Andere Bezeichnung: C19orf29 (CACTIN Produkte)

Synonyme: C19orf29 antikoerper, NY-REN-24 antikoerper, fSAPc antikoerper, C28H19orf29 antikoerper, 2510012J08Rik antikoerper, cactin, spliceosome C complex subunit antikoerper, CACTIN antikoerper, Cactin antikoerper

Hintergrund:

Synonyms: C19orf29, Cactin, CS029_HUMAN, FLJ17482, FLJ59622, fSAPc, Renal carcinoma antigen NY-REN-24, Uncharacterized protein C19orf29.

Background: Consisting of around 63 million bases with over 1,400 genes, chromosome 19 makes up over 2 % of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fc?receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3. The C19orf29 gene product has been provisionally designated C19orf29 pending further characterization.

Pathways: Cellular Response to Molecule of Bacterial Origin