CEP290 Monoclonal antibody, PBS Only

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  WB analysis using 67716-1-Ig (same clone as 67716-1-PBS)

  Various lysates were subjected to SDS PAGE followed by western blot with 67716-1-Ig (CEP290 antibody) at dilution of 1:2000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 67716-1-PBS in a different storage buffer formulation.

• 

  WB analysis of HSC-T6 using 67716-1-Ig (same clone as 67716-1-PBS)

  HSC-T6 cells were subjected to SDS PAGE followed by western blot with 67716-1-Ig (CEP290 antibody) at dilution of 1:2000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 67716-1-PBS in a different storage buffer formulation.

CEP290 Monoclonal Antibody for WB, Indirect ELISA

Cat No. 67716-1-PBS

Clone No.2C10G2

Host / Isotype

Mouse / IgG2b

Reactivity

Human, rat, mouse

Applications

WB, Indirect ELISA

Synonyms

3H11Ag, BBS14, Cancer/testis antigen 87, centrosomal protein 290kDa, Centrosomal protein of 290 kDa, CEP290, CT87, FLJ13615, FLJ21979, JBTS5, JBTS6, KIAA0373, LCA10, MKS4, Nephrocystin 6, rd16, SLSN6, Tumor antigen se2 2

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Product Information

67716-1-PBS targets CEP290 in WB, Indirect ELISA applications and shows reactivity with Human, rat, mouse samples.

• Tested Reactivity: Human, rat, mouse
• Host / Isotype: Mouse / IgG2b
• Class: Monoclonal
• Type: Antibody
• Immunogen: CEP290 fusion protein Ag17457
• Full Name: centrosomal protein 290kDa
• Calculated Molecular Weight: 2479 aa, 290 kDa
• Observed Molecular Weight: 290 kDa
• GenBank Accession Number: BC008641
• Gene Symbol: CEP290
• Gene ID (NCBI): 80184
• RRID: AB_2918499
• Conjugate: Unconjugated
• Form: Liquid
• Purification Method: Protein A purification
• UNIPROT ID: O15078
• Storage Buffer: PBS Only
• Storage Conditions: Store at -80°C.

Background Information

Studies in the Chlamydomonas model system has shown that the ciliary protein CEP290 is a critical component of these Y-link junctions. Additionally, numerous studies have demonstrated that CEP290's function is critical for IFT-in CEP290 knockdown experiments, many proteins that would normally localize to the cilium fail to do so, and cilium formation is disrupted or absent. Mutations in CEP290 are accountable for cases of nephronophthisis, Leber congenital amaurosis and Joubert syndrome. In IF analtsis of HeLa cells, the white arrows show centrosome and cilium staining. Two isoforms were produced by alternative splicing with predicted MW of 290 and 180 kDa according to UniProt.