Rabbit Anti-CCNC Recombinant Antibody (EG515) (CBMAB-EN585-LY)

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Basic Information

Host Animal
Rabbit
Clone
EG515
Application
WB, IP, IF, FC
Immunogen
Synthetic peptide corresponding to residues surrounding Pro263 of human cyclin C protein.
Host Species
Rabbit
Specificity
Human, Mouse
Antibody Isotype
IgG
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.
ApplicationNote
WB1:1,000
IP1:100
IF(ICC)1:1,600-1:6,400
FC1:100-1:400

Formulations & Storage [For reference only, actual COA shall prevail!]

Format
Liquid
Buffer
HEPES, pH 7.5, 100 µg/ml BSA, 50% glycerol
Preservative
0.02% sodium azide
Concentration
Batch dependent
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freezethaw cycles.
More Infomation

Target

Full Name
Cyclin C
Introduction
CCNC (Cyclin C) is a Protein Coding gene. Among its related pathways are Signaling by NOTCH1 and Gene Expression. Gene Ontology (GO) annotations related to this gene include protein kinase binding. An important paralog of this gene is CCNK.
Entrez Gene ID
Human892
Mouse51813
Rat114839
UniProt ID
HumanP24863
MouseQ62447
RatP39947
Alternative Names
Cyclin C; SRB11 Homolog; HSRB11; Cyclin-C; SRB11; CycC;
Function
Component of the Mediator complex, a coactivator involved in regulated gene transcription of nearly all RNA polymerase II-dependent genes. Mediator functions as a bridge to convey information from gene-specific regulatory proteins to the basal RNA polymerase II transcription machinery. Mediator is recruited to promoters by direct interactions with regulatory proteins and serves as a scaffold for the assembly of a functional preinitiation complex with RNA polymerase II and the general transcription factors. Binds to and activates cyclin-dependent kinase CDK8 that phosphorylates the CTD (C-terminal domain) of the large subunit of RNA polymerase II (RNAp II), which may inhibit the formation of a transcription initiation complex.
Biological Process
Positive regulation of transcription by RNA polymerase II Source: GO_Central
Regulation of transcription by RNA polymerase II Source: GO_Central
Regulation of transcription initiation from RNA polymerase II promoter Source: Reactome
Cellular Location
Nucleus

Tang, M., Pei, G., Su, D., Wang, C., Feng, X., Srivastava, M., ... & Chen, J. (2021). Genome-wide CRISPR screens reveal cyclin C as synthetic survival target of BRCA2. Nucleic acids research, 49(13), 7476-7491.

Lloyd, R. L., Urban, V., Muñoz-Martínez, F., Ayestaran, I., Thomas, J. C., de Renty, C., ... & Jackson, S. P. (2021). Loss of Cyclin C or CDK8 provides ATR inhibitor resistance by suppressing transcription-associated replication stress. Nucleic acids research, 49(15), 8665-8683.

Ponce, J. M., Coen, G., Spitler, K. M., Dragisic, N., Martins, I., Hinton Jr, A., ... & Grueter, C. E. (2020). Stress‐Induced Cyclin C Translocation Regulates Cardiac Mitochondrial Dynamics. Journal of the American Heart Association, 9(7), e014366.

Stieg, D. C., Cooper, K. F., & Strich, R. (2020). The extent of cyclin C promoter occupancy directs changes in stress-dependent transcription. Journal of Biological Chemistry, 295(48), 16280-16291.

Jezek, J., Wang, K., Yan, R., Di Cristofano, A., Cooper, K. F., & Strich, R. (2019). Synergistic repression of thyroid hyperplasia by cyclin C and Pten. Journal of cell science, 132(16), jcs230029.

Ježek, J., Smethurst, D. G., Stieg, D. C., Kiss, Z. A. C., Hanley, S. E., Ganesan, V., ... & Strich, R. (2019). Cyclin C: The story of a non-cycling cyclin. Biology, 8(1), 3.

Jezek, J., Chang, K. T., Joshi, A. M., & Strich, R. (2019). Mitochondrial translocation of cyclin C stimulates intrinsic apoptosis through Bax recruitment. EMBO reports, 20(9), e47425.

Stieg, D. C., Chang, K. T., Cooper, K. F., & Strich, R. (2019). Cyclin C regulated oxidative stress responsive transcriptome in Mus musculus embryonic fibroblasts. G3: Genes, Genomes, Genetics, 9(6), 1901-1908.

Ganesan, V., Willis, S. D., Chang, K. T., Beluch, S., Cooper, K. F., & Strich, R. (2019). Cyclin C directly stimulates Drp1 GTP affinity to mediate stress-induced mitochondrial hyperfission. Molecular biology of the cell, 30(3), 302-311.

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For research use only. Not intended for any clinical use.

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