CACTIN antibody (AbBy Fluor® 488)

Catalog No. ABIN1405684

Product Details anti-CACTIN Antibody (AbBy Fluor® 488)

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

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CACTIN antibody is conjugated to AbBy Fluor® 488

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

Cross-Reactivity: Human, Mouse, Rat

Purification: Purified by Protein A.

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

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200

Restrictions: For Research Use only

Handling

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.

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Storage: -20 °C

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

Expiry Date: 12 months

Target Details for CACTIN

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

Alternative Name: C19orf29 (CACTIN Products)

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

Background:

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