type
Type III
form
lyophilized powder
specific activity
≥25 units/mg protein (biuret)
mol wt
dimer 110 kDa
foreign activity
glucose-6-phosphate dehydrogenase and phosphoglucose isomerase ≤10%
storage temp.
−20°C
Gene Information
bakers yeast ... HXK1(850614), HXK2(852639)
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Biochem/physiol Actions
以ATP作为磷酸盐来源,催化C6位的 D-己糖的磷酸化。
不同的己糖具有不同的磷酸化速率(pH 7.5,30 °C)。
D-果糖 KM:0.33 mM
D-葡萄糖 KM:0.12 mM
D-甘露糖 KM:0.05 mM
酵母己糖激酶具有两种相似的亚型,即PI和PII(A和B), 其等电点分别为5.25和4。
分子量: ~ 54 kDa (单体)
~110 kDa (二聚体)
最适pH:7.5至9.0
消光系数:在280 nm处,E1% = 8.85 (PI)和9.47 (PII)
活化剂:己糖激酶的活化需要 Mg2+ 离子(KM = 2.6 mM)。 己糖激酶可被儿茶酚胺及其相关化合物激活。
抑制剂:山梨糖-1-磷酸,多磷酸盐,6-脱氧-6-氟葡萄糖,2-C-羟基-甲基葡萄糖,木糖,来苏糖和硫醇反应性化合物(Hg2+ 和4-氯代苯甲酸酯)
不同的己糖具有不同的磷酸化速率(pH 7.5,30 °C)。
D-果糖 KM:0.33 mM
D-葡萄糖 KM:0.12 mM
D-甘露糖 KM:0.05 mM
酵母己糖激酶具有两种相似的亚型,即PI和PII(A和B), 其等电点分别为5.25和4。
分子量: ~ 54 kDa (单体)
~110 kDa (二聚体)
最适pH:7.5至9.0
消光系数:在280 nm处,E1% = 8.85 (PI)和9.47 (PII)
活化剂:己糖激酶的活化需要 Mg2+ 离子(KM = 2.6 mM)。 己糖激酶可被儿茶酚胺及其相关化合物激活。
抑制剂:山梨糖-1-磷酸,多磷酸盐,6-脱氧-6-氟葡萄糖,2-C-羟基-甲基葡萄糖,木糖,来苏糖和硫醇反应性化合物(Hg2+ 和4-氯代苯甲酸酯)
Physical form
Lyophilized powder containing approx. 15% sodium citrate
Other Notes
One unit will phosphorylate 1.0 μmole of D-glucose per min at pH 7.6 at 25 °C, unless otherwise indicated below.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
François Vaillant et al.
Cancer cell, 24(1), 120-129 (2013-07-13)
The prosurvival protein BCL-2 is frequently overexpressed in estrogen receptor (ER)-positive breast cancer. We have generated ER-positive primary breast tumor xenografts that recapitulate the primary tumors and demonstrate that the BH3 mimetic ABT-737 markedly improves tumor response to the antiestrogen
Seok-Hyung Kim et al.
PLoS genetics, 9(6), e1003563-e1003563 (2013-06-21)
Multiple Acyl-CoA Dehydrogenase Deficiency (MADD) is a severe mitochondrial disorder featuring multi-organ dysfunction. Mutations in either the ETFA, ETFB, and ETFDH genes can cause MADD but very little is known about disease specific mechanisms due to a paucity of animal
Charles Betz et al.
The Journal of cell biology, 203(4), 563-574 (2014-01-05)
Target of rapamycin (TOR) forms two conserved, structurally distinct kinase complexes termed TOR complex 1 (TORC1) and TORC2. Each complex phosphorylates a different set of substrates to regulate cell growth. In mammals, mTOR is stimulated by nutrients and growth factors
Markus Weiler et al.
Proceedings of the National Academy of Sciences of the United States of America, 111(1), 409-414 (2013-12-25)
A hypoxic microenvironment induces resistance to alkylating agents by activating targets in the mammalian target of rapamycin (mTOR) pathway. The molecular mechanisms involved in this mTOR-mediated hypoxia-induced chemoresistance, however, are unclear. Here we identify the mTOR target N-myc downstream regulated
Takayuki Hoshii et al.
Proceedings of the National Academy of Sciences of the United States of America, 111(10), 3805-3810 (2014-02-26)
mTOR is an evolutionarily conserved kinase that plays a critical role in sensing and responding to environmental determinants. Recent studies have shown that fine-tuning of the activity of mTOR complexes contributes to organogenesis and tumorigenesis. Although rapamycin, an allosteric mTOR
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