epitope corresponding to amino acids 1-360 representing the kinase domain of GAK (cyclin G associated kinase) of rat origin
Modification Notes
Cyclins are the regulatory subunits of Cdc2 p34 and related cyclin-dependent kinases (Cdks) which play critical roles in the control of cell cycle progression. The catalytic subunit for cyclin A and B is Cdc2 p34 kinase. The Cdc2-cyclin B complex controls the G2 to M transition whereas Cdc2-cyclin A regulates S phase progression (1,2). The G1 to S transition, however, appears to be controlled by the G1 cyclins (1,2). Cyclin D1 accumulates during G1 and associates with Cdk2, Cdk4 and Cdk5 (3-5). Cyclin E and Cdk2 interact during the G1 to S transition (6). Cyclin G contains a typical N terminal cyclin box and a carboxy terminal domain sequence homologous to the tyrosine phosphorylation site of the epidermal growth factor receptor (7). Cyclin G expression is induced within 3 hours after growth stimulation and remains elevated with no apparent cell cycle dependency (7). A serine/threonine kinase, designated GAK for cyclin G associated kinase, has been identified. GAK has been shown to bind directly to cyclin G and to co-immunoprecipitate with Cdk5, which also associates with cyclin G (8).
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPIFELISA
recommended for GAK of mouse, rat and human origin by WB, IP, IF and ELISA:
Species Reactivity
HumanMouseRat
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Alternative Names
epitope corresponding to amino acids 1-360 representing the kinase domain of GAK (cyclin G associated kinase) of rat origin
Tissue Specificity
epitope corresponding to amino acids 1-360 representing the kinase domain of GAK (cyclin G associated kinase) of rat origin