FoxO1A (Acetyl Lys248) rabbit pAb
Disease: Chromosomal aberrations involving FOXO1 are a cause of rhabdomyosarcoma 2 (RMS2) [MIM: 268220]; also known as alveolar rhabdomyosarcoma. Translocation (2;13) (q35;q14) with PAX3; translocation t (1;13) (p36;q14) with PAX7. The resulting protein is a transcriptional activator. function: Transcription factor. PTM: Phosphorylated by AKT1; insulin-induced (By similarity). IGF1 rapidly induces phosphorylation of Ser-256, Thr-24, and Ser-319. Phosphorylation of Ser-256 decreases DNA-binding activity and promotes the phosphorylation of Thr-24, and Ser-319, permitting phosphorylation of Ser-322 and Ser-325, probably by CK1, leading to nuclear exclusion and loss of function. Phosphorylation of Ser-329 is independent of IGF1 and leads to reduced function. Phosphorylated upon DNA damage, probably by ATM or ATR. similarity: Contains 1 fork-head DNA-binding domain. subcellular location: Shuttles between cytoplasm and nucleus. subunit: Interacts with LRPPRC. tissue specificity: Ubiquitous.
Product Specifications
Background
UniProt
Q12778
Swiss Prot
Q12778
Reactivity
Human; Mouse; Rat
Immunogen
Synthesized peptide derived from human FoxO1A (Acetyl Lys248)
Clonality
Polyclonal
Source
Rabbit
Applications
WB; ELISA
Concentration
1 mg/ml
Dilution
WB 1:1000-2000 ELISA 1:5000-20000
Molecular Weight
72kD
Storage Conditions
-20°C/1 year
Observed Molecular Weight
72kD
Fragment
IgG
Subcellular Location
Other Product Names
Forkhead box protein O1 (Forkhead box protein O1A; Forkhead in rhabdomyosarcoma)
Gene ID (Human)
2308
Available Sizes
Explore Other Products
Discover premium biology products from our extensive collection of 20M+ items