MABN2248

Anti-SDCCAG8 Antibody, clone 12D7.1

clone 12D7.1, from mouse

• Synonym(s): Serologically defined colon cancer antigen 8, Antigen NY-CO-8, Centrosomal colon cancer autoantigen protein, hCCCAP
• UNSPSC Code: 12352203
• eCl@ss: 32160702
• NACRES: NA.41

Properties

• biological source: mouse
• Quality Level: 100
• antibody form: purified immunoglobulin
• antibody product type: primary antibodies
• clone: 12D7.1, monoclonal
• species reactivity: human
• technique(s): western blot: suitable
• isotype: IgG1κ
• NCBI accession no.: NP_006633
• UniProt accession no.: Q86SQ7
• shipped in: ambient
• target post-translational modification: unmodified
• Gene Information: human ... SDCCAG8(10806)

Description

General description

Serologically defined colon cancer antigen 8 (UniProt: Q86SQ7; also known as Antigen NY-CO-8, Centrosomal colon cancer autoantigen protein, hCCCAP, SDCCAG8) is encoded by the SDCCAG8 (also known as CCCAP, NPHP10) gene (Gene ID: 10806) in human. Serologically defined colon cancer antigen 8 is a homodimeric cell junction protein that regulates centrosomal accumulation of pericentriolar material (PCM) and neuronal polarization and migration in the developing cortex. SDCCAG8 protein interacts and cotraffics with PCM, which is shown to be crucial for targeting proteins to the centrosome. It also plays a role in the establishment of cell polarity and epithelial lumen formation and may also play a role in ciliogenesis. Four isoforms of SDCCAG8 protein have been described that are produced by alternative splicing. SDCCAG8 protein has 3 coiled coil regions (aa 129-175; 223-273; and 348-707). SDCCAG8 gene expression is shown to be selectively elevated in newborn neurons prior to their commencement of radial locomotion. Mutations in this gene results in neuronal migration defects. Mutations in SDCCAG8 gene are linked to Senior-Loken syndrome 7 (SLSN7), a renal-retinal disorder, which is characterized by progressive wasting of the filtering unit of the kidney (nephronophthisis), with or without medullary cystic renal disease, and progressive eye disease. In addition some mutations can cause Bardet-Biedl syndrome 16 (BBS16), which is characterized by severe pigmentary retinopathy, early-onset obesity, renal malformation, and mental retardation. (Ref.: Insolera, R., et al. (2014). Neuron 83(4); 805 822).

Specificity

Clone 12D7.1 detects Serologically defined colon cancer antigen 8 (SDCCAG8) in human cells. It targets an epitope within 101 amino acids from the N-terminal half.

Immunogen

GST/His-tagged recombinant fragment corresponding to 101 amino acids from the N-terminal half of human Serologically defined colon cancer antigen 8. This immuogen sequence is conserved in isoforms 1 and 2.

Application

Anti-SDCCAG8, clone 12D7.1, Cat. No. MABN2248, is a highly specific mouse monoclonal antibody that targets SDCCAG8 and has been tested for use in Western Blotting.

Western Blotting Analysis (WB): A 1:2000 Dilution of this antibody detected SDCCAG8 in SDCCAG8 overexpressed HEK293 lysate.
Western Blotting Analysis (WB): A 1:1000 Dilution of this antibody detected SDCCAG8 in U251 and human tonsil.

Quality

Evaluated by Western Blotting in U251 cell lysate.
Western Blotting Analysis (WB): A 1:1000 Dilution of this antibody detected SDCCAG8 in U251 cell lysate.

Target description

~65 kDa observed; 82.68 kDa calculated. Uncharacterized bands may be observed in some lysate(s).

Physical form

Format: Purified

Other Notes

Concentration: Please refer to lot specific datasheet.

Safety Information

• Storage Class: 12 - Non Combustible Liquids
• wgk_germany: WGK 1