Technical Data
C2550-06B
Cdc6, phosphorylated (Ser106) (CDC18L, HsCDC18, HsCDC6, p62cdc6, Cell Division Cycle 6)
Description:
The Cdc6 protein is an essential component of pre-replication complexes (preRCs), which assemble at origins of DNA replication during the G1 phase of the cell cycle (1). Cdc6 participates in checkpoint controls that ensure DNA replication is completed before mitosis is initiated 2). It has been concluded that expression of Cdc6 is regulated in response to mitogenic signals though transcriptional control mechanisms involving E2F proteins, and that Cdc6 is required for initiation of DNA replication in mammalian cells (3). In vitro, Cdc6 is an excellent substrate for Cdk2, phosphorylated at three sites (Serine 54, Serine 74 and Serine 106) (4).

Applications:
Suitable for use in Western Blot. Other applications not tested.

Recommended Dilution:
Western Blot: 1:1000-2000
Optimal dilutions to be determined by the researcher.

Storage and Stability:
May be stored at 4°C for short-term only. For long-term storage, store at -20°C. Aliquots are stable for at least 12 months at -20°C. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Further dilutions can be made in assay buffer.

Manufactured incorporating RabMAb® technology under Epitomics US patents, No 5,675,063 and 7,429,487, owned by Abcam.
TypeIsotypeCloneGrade
MabIgG9E213Supernatant
SizeStorageShippingSourceHost
100ul-20°CBlue IceHumanRabbit
Concentration:
Not determined
Immunogen:
A phospho-specific peptide corresponding to residues surrounding Serine 106 of human Cdc6.
Purity:
Supernatant
Form
Supplied as a liquid in 50mM Tris-glycine, pH 7.4, 0.15M sodium chloride, 40% glycerol, 0.01% sodium azide, 0.05% BSA.
Specificity:
Recognizes Cdc6 phosphorylated on Serine 106.
Intended for research use only. Not for use in human, therapeutic, or diagnostic applications.
1. Hall JR, et al. Mol Biol Cell. 18(9):3340-50, 2007. 2. Williams RS, et al. Proc Natl Acad Sci U S A. 94(1):142-7, 1997. 3. Yan Z, et al. Proc Natl Acad Sci U S A. 95(7):3603-8, 1998 4. Jiang W, et al. Proc Natl Acad Sci U S A. 96(11):6193-8, 1999.