epitope corresponding to phosphorylated Thr 1462 of tuberin of human origin
Modification
Phosphoralated
Modification Notes
Hamartin (TSC1) and tuberin (TSC2, LAM, TSC4) can form a functional complex and negatively regulate cell growth by inhibiting protein synthesis. Tuberous sclerosis complex (TSC) is a genetic disorder that arises through mutations in the hamartin and tuberin genes. The phosphoinositide 3-kinase (PI3K)/Akt pathway phosphorylates tuberin on serine-939 and threonine-1462 and inhibits the tumor suppressor function of the TSC complex. Anisomycin stimulates phosphorylation of serine-1210 of tuberin via the p38-MK2 kinase cascade. Phosphorylation of tuberin by MK2 creates a 14-3-3 binding site. Phosphorylation of hamartin regulates the function of the hamartin-tuberin complex during the G2/M phase of the cell cycle.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIFELISA
recommended for detection of Thr 1462 phosphorylated tuberin of mouse, rat and human origin by WB, IF and ELISA also reactive with additional species, including equine, canine and porcine:
Species Reactivity
HumanMouseRat
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Alternative Names
epitope corresponding to phosphorylated Thr 1462 of tuberin of human origin
Tissue Specificity
epitope corresponding to phosphorylated Thr 1462 of tuberin of human origin
recommended for detection of Thr 1462 phosphorylated tuberin of mouse, rat and human origin by WB, IF and ELISA also reactive with additional species, including equine, canine and porcine:
Additional Information
Form
Liquid
Storage Instructions
For short-term storage, store at 4° C. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.