CACTIN anticorps (Cy3)

N° du produit ABIN1423553

Détail du produit anti-CACTIN anticorps (Cy3)

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CACTIN est conjugé à/à la Cy3

Application: Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by Protein A.

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

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur CACTIN

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

Autre désignation: C19orf29 (CACTIN Produits)

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

Sujet:

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