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CCDC8 encodes a coiled-coil domain-containing protein. Additionally we are shipping Coiled-Coil Domain Containing 8 Kits (20) and Coiled-Coil Domain Containing 8 Proteins (3) and many more products for this protein.
Showing 10 out of 35 products:
Human Polyclonal CCDC8 Primary Antibody for EIA, IHC (p) - ABIN951121
Simpson, Wellenreuther, Poustka, Pepperkok, Wiemann: Systematic subcellular localization of novel proteins identified by large-scale cDNA sequencing. in EMBO reports 2001
Human Polyclonal CCDC8 Primary Antibody for WB - ABIN949718
Hanson, Murray, OSullivan, Urquhart, Daly, Bhaskar, Biesecker, Skae, Smith, Cole, Kirk, Chandler, Kingston, Donnai, Clayton, Black: Exome sequencing identifies CCDC8 mutations in 3-M syndrome, suggesting that CCDC8 contributes in a pathway with CUL7 and OBSL1 to control human growth. in American journal of human genetics 2011
CUL7 (show CUL7 Antibodies), OBSL1 and CCDC8 modulate the alternative splicing of the INSR (show INSR Antibodies)
The CUL7 (show CUL7 Antibodies), OBSL1, and CCDC8 proteins form a 3M complex that functions in maintaining microtubule and genome integrity and normal development.
Mutations in CUL7 (show CUL7 Antibodies), OBSL1 and CCDC8 in 3-M syndrome lead to disordered growth factor signalling.
discussion of roles of CCDC8, CUL7 (cullin 7), and OBSL1 (obscurin-like 1) in growth and development using findings from patients with Miller-McKusick-Malvaux syndrome and Silver-Russell syndrome [REVIEW]
p90 (show CANX Antibodies) is a critical cofactor for p53 (show TP53 Antibodies)-mediated apoptosis through promoting Tip60 (show KAT5 Antibodies)-mediated p53 (show TP53 Antibodies) acetylation.
We propose that CUL7 (show CUL7 Antibodies), OBSL1, and CCDC8 are members of a pathway controlling mammalian growth.
This gene encodes a coiled-coil domain-containing protein. The encoded protein functions as a cofactor required for p53-mediated apoptosis following DNA damage, and may also play a role in growth through interactions with the cytoskeletal adaptor protein obscurin-like 1. Mutations in this gene are a cause of 3M syndrome-3 (3M3).
coiled-coil domain-containing protein 8
, protein phosphatase 1, regulatory subunit 20
, probable Coiled-coil domain-containing protein 8
, coiled-coil domain-containing protein 8 homolog