DATASHEET
Host:
Rabbit
Target Protein:
Phospho-GCN2 (Thr899)
Specificity:
This phosphorylation site is homologous to Thr898 in Mouse and Thr899 in Rat.
Modification Site:
Thr899
Clonality:
Polyclonal
Isotype:
IgG
Entrez Gene:
440275
Swiss Prot:
Q9P2K8
Source:
KLH conjugated synthetic phosphopeptide derived from human GCN2 around the phosphorylation site of Thr899
Purification:
Purified by Protein A.
Storage Buffer:
Aqueous buffered solution containing 0.01M TBS (pH 7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Storage:
Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
Background:
GCN2 belongs to a family of kinases that phosphorylate the alpha subunit of eukaryotic translation initiation factor 2 to downregulate protein synthesis in response to varied cellular stresses.
Conjugation:
FITC
Excitation/ Emission:
494nm/518nm
Size:
100µL
Concentration:
1ug/ul
Applications:
WB(1:300-5000)
ELISA(1:500-1000)
FCM(1:20-100)
189
Human
Mouse
Predicted Cross Reactive Species:
Rat
Dog
Cow
Horse
For research use only. Not intended for diagnostic or therapeutic use.
PRODUCT SPECIFIC PUBLICATIONS
- Lehman, Stacey L., Sandra Ryeom, and Constantinos Koumenis. "Signaling through alternative Integrated Stress Response pathways compensates for GCN2 loss in a mouse model of soft tissue sarcoma." Scientific Reports 5 (2015).Read more>>
- Changzheng Li. et al. Amino acid catabolism regulates hematopoietic stem cell proteostasis via a GCN2-eIF2_ axis. CELL STEM CELL. 2022 Jul;29:1119Read more>>
- Zikang Xing. et al. IDO1 Inhibitor RY103 Suppresses Trp-GCN2-Mediated Angiogenesis and Counters Immunosuppression in Glioblastoma. PHARMACEUTICS. 2024 Jul;16(7):87Read more>>
VALIDATION IMAGES
Molt-4cells were fixed with 4% PFA for 10min at room temperature,permeabilized with 90% ice-cold methanol for 20 min at -20℃, and incubated in 5% BSA blocking buffer for 30 min at room temperature. Cells were then stained with GCN2 (Thr899) Polyclonal Antibody(bs-3155R-FITC)at 1:50 dilution in blocking buffer and incubated for 30 min at room temperature, washed twice with 2%BSA in PBS. Acquisitions of 20,000 events were performed. Cells stained with primary antibody (green), and isotype control (orange).