Rabbit Polyclonal TIGAR antibody. Suitable for IHC-P, WB and reacts with Human, Rat, Mouse samples. Cited in 4 publications. Immunogen corresponding to Synthetic Peptide within Human TIGAR aa 100-200.
View Alternative Names
C12orf5, TIGAR, TP53-induced glycolysis and apoptosis regulator, TP53-induced glycolysis regulatory phosphatase
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TIGAR antibody (AB189164)
Immunohistochemical analysis of formalin/PFA-fixed paraffin-embedded human brain cerebellum tissue sections labeling TIGAR using ab189164 at 10 μg/ml.
- WB
Supplier Data
Western blot - Anti-TIGAR antibody (AB189164)
Lanes 1 - 2:
Western blot - Anti-TIGAR antibody (ab189164) at 1 µg/mL
Lane 3:
Western blot - Anti-TIGAR antibody (ab189164) at 4 µg/mL
Lane 4:
Western blot - Anti-TIGAR antibody (ab189164) at 2 µg/mL
Lane 1:
Human liver lysate
Lane 2:
Human liver lysate plus immunizing peptide
Lane 3:
Mouse liver lysate
Lane 4:
Rat liver lysate
Predicted band size: 30 kDa
false
Reactivity data
Properties and storage information
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Supplementary information
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Biological function summary
TIGAR plays a critical role in controlling the oxidative stress within cells. By lowering glycolytic rates it shifts cellular metabolism toward the pentose phosphate pathway boosting the production of NADPH and reducing reactive oxygen species (ROS). This protein does not form a part of a larger complex operating independently to exhibit its effects. It also influences cellular survival mechanisms by mitigating oxidative stress which is important for cell health.
Pathways
TIGAR is involved with both apoptosis and carbohydrate metabolism pathways where it acts to support cellular metabolism and survival. Within these pathways it interacts closely with the tumor suppressor protein p53 which regulates TIGAR expression. Another related protein is AMPK which also plays roles in energy balance and is influenced by changes in cellular metabolic status. TIGAR's actions help in cellular adaptation during metabolic stress maintaining energy homeostasis.
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Target data
Publications (4)
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American journal of translational research 17:1223-1236 PubMed40092124
2025
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Nature communications 15:4340 PubMed38773142
2024
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Unspecified reactive species
BMC complementary medicine and therapies 22:188 PubMed35840932
2022
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Stem cells (Dayton, Ohio) 37:937-947 PubMed30977208
2019
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Product promise
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