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| 氨基酸 |
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G4251 | CAS:70-18-8 | L-Glutathione reduced | L-谷胱甘肽(还原型)
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G4251 L-Glutathione reduced
Sigma-Aldrich ≥98.0%
窗体底端
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货号
号 |
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目录价
RMB |
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G4251-10MG |
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180.18 |
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G4251-500G |
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6,399.90 |
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G4251-300MG |
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200.07 |
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G4251-1G |
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219.96 |
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G4251-5G |
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259.74 |
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G4251-10G |
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400.14 |
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G4251-25G |
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600.21 |
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G4251-50G |
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1,000.35 |
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G4251-100G |
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1,799.46 |
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G4251-250G |
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3,800.16 |
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Synonym: |
γ-L-Glutamyl-L-cysteinyl-glycine, GSH |
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Amino Acid Sequence: |
γ-Glu-Cys-Gly |
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CAS Number: |
70-18-8 |
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Linear Formula: |
H2NCH(CO2H)CH2CH2CONHCH(CH2SH)CONHCH2CO2H |
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Molecular Weight: |
307.32 |
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Beilstein Registry Number: |
1729812 |
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EC Number: |
200-725-4 |
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MDL number: |
MFCD00065939 |
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PubChem Substance ID: |
24895164 |
Description
| Frequently Asked Questions |
Live Chat and Frequently Asked Questions are available for this Product. |
| Application |
May be used at 5-10 mM to elute glutathione S-transferase (GST) from glutathione agarose. |
| Biochem/physiol Actions |
Endogenous antioxidant that plays a major role in reducing reactive oxygen species formed during cellular metabolism and the respiratory burst. Glutathione-S-transferase catalyzes the formation of glutathione thioethers with xenobiotics, leukotrienes, and other molecules that have an electrophilic center. Glutathione also forms disulfide bonds with cysteine residues in proteins. Via these mechanisms, it can have the paradoxical effect of reducing the efficacy of anti-cancer agents. |
| Packaging |
10 mg in autosmp vl |
性质
| assay |
≥98.0% |
| EQP level |
Premium |
| mp |
192-195 °C (dec.)(lit.) |
| storage temp. |
2-8°C |
安全性
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