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CCDC8 encodes a coiled-coil domain-containing protein. Additionally we are shipping Coiled-Coil Domain Containing 8 Antibodies (41) and Coiled-Coil Domain Containing 8 Proteins (3) and many more products for this protein.
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Variants near TTN (show TTN ELISA Kits) and CCDC8 were associated with KI67 (show MKI67 ELISA Kits) expression, and rs2288563 and rs2562832 in TTN (show TTN ELISA Kits) are potential biomarkers for the prediction of clinical outcomes in hepatitis B-related hepatocellular carcinoma patients.
CCDC8 may suppress the invasion and metastasis of non-small cell lung cancer cells.
CUL7 (show CUL7 ELISA Kits), OBSL1 and CCDC8 modulate the alternative splicing of the INSR (show INSR ELISA Kits)
The CUL7 (show CUL7 ELISA Kits), OBSL1, and CCDC8 proteins form a 3M complex that functions in maintaining microtubule and genome integrity and normal development.
Mutations in CUL7 (show CUL7 ELISA Kits), 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 ELISA Kits) is a critical cofactor for p53 (show TP53 ELISA Kits)-mediated apoptosis through promoting Tip60 (show KAT5 ELISA Kits)-mediated p53 (show TP53 ELISA Kits) acetylation.
We propose that CUL7 (show CUL7 ELISA Kits), 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