(+)-Catechin hydrate(Synonyms: (+)-水合儿茶素)

天然产物 黄酮类 Flavonoids

(+)-Catechin hydrate (Synonyms: (+)-水合儿茶素) 纯度: 99.59%

(+)-Catechin hydrate 抑制环加氧酶-1 (COX-1) , IC50 为 1.4 μM。

(+)-Catechin hydrate(Synonyms: (+)-水合儿茶素)

(+)-Catechin hydrate Chemical Structure

CAS No. : 225937-10-0

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500 mg   询价  

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  • Clinical Compound Library
  • Anti-Aging Compound Library
  • Drug Repurposing Compound Library
  • Diabetes Related Compound Library
  • Anti-COVID-19 Compound Library
  • Traditional Chinese Medicine Monomer Library
  • Flavonoids Library
  • Food-Sourced Compound Library

生物活性

(+)-Catechin hydrate inhibits cyclooxygenase-1 (COX-1) with an IC50 of 1.4 μM.

IC50 & Target[1]

COX-1

1.4 μM (IC50)

体外研究
(In Vitro)

(+)-Catechin exhibits >95% inhibitory activity at 70 μg/mL against cyclooxygenase-1 (COX-1) with an IC50 of 1.4 μM[1]. A dose-dependent reduction in color is observed after 24 hours of treatment with (+)-Catechin, and 54.76% of the cells are dead at the highest concentration of (+)-Catechin tested (160 μg/mL) whereas the IC50 of (+)-Catechin is achieved at 127.62 μg/mL (+)-Catechin. A dose- and time-dependent increase in the induction of apoptosis is observed when MCF-7 cells are treated with (+)-Catechin. When compare to the control cells at 24 hours, 40.7 and 41.16% of the cells treated with 150 μg/mL and 300 μg/mL (+)-Catechin, respectively, undergo apoptosis. The expression levels of Caspase-3, -8, and -9 and p53 in MCF-7 cells treated with 150 μg/mL (+)-Catechin for 24 h increase by 5.81, 1.42, 3.29, and 2.68 fold, respectively, as compare to the levels in untreated control cells[2].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究
(In Vivo)

Animals treated with (+)-Catechin at the lowest tested dose, i.e., 50 mg/kg, p.o. have spent comparatively more time in exploring the novel object in the choice trial, however, the difference is not statistically significant. (+)-Catechin prevents the time-induced episodic memory deficits in a dose-dependent manner, the most effective being 200 mg/kg, p.o.. Treatment with (+)-Catechin prevents the rise in MPO level compare to DOX alone treatment group (21.98±9.44 and 36.76±4.39% in the hippocampus and the frontal cortex respectively)[3].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

Clinical Trial

Formula

C15H14O6.xH2O

CAS 号

225937-10-0

中文名称

(+)-水合儿茶素

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
溶解性数据
In Vitro: 

DMSO : 50 mg/mL (Need ultrasonic)

In Vivo:

请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液,再依次添加助溶剂:

——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
分比是指该溶剂在您配制终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶

  • 1.

    请依序添加每种溶剂: 10% DMSO    40% PEG300    5% Tween-80    45% saline

    Solubility: ≥ 2.5 mg/mL (Infinity mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (Infinity mM,饱和度未知) 的澄清溶液。

    以 1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中,混合均匀;向上述体系中加入50 μL Tween-80,混合均匀;然后继续加入 450 μL生理盐水定容至 1 mL。

    将 0.9 g 氯化钠,完全溶解于 100 mL ddH₂O 中,得到澄清透明的生理盐水溶液

  • 2.

    请依序添加每种溶剂: 10% DMSO    90% (20% SBE-β-CD in saline)

    Solubility: ≥ 2.5 mg/mL (Infinity mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (Infinity mM,饱和度未知) 的澄清溶液。

    以 1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 900 μL 20% 的 SBE-β-CD 生理盐水水溶液中,混合均匀。

    将 2 g 磺丁基醚 β-环糊精加入 5 mL 生理盐水中,再用生理盐水定容至 10 mL,完全溶解,澄清透明
  • 3.

    请依序添加每种溶剂: 10% DMSO    90% corn oil

    Solubility: ≥ 2.5 mg/mL (Infinity mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (Infinity mM,饱和度未知) 的澄清溶液,此方案不适用于实验周期在半个月以上的实验。

    以 1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 900 μL玉米油中,混合均匀。

*以上所有助溶剂都可在 Shanghai Jinpan Biotech Co Ltd 网站选购。
参考文献
  • [1]. Waffo-Téguo P, et al. Potential cancer-chemopreventive activities of wine stilbenoids and flavans extracted from grape (Vitis vinifera) cell cultures. Nutr Cancer. 2001;40(2):173-9.

    [2]. Alshatwi AA. Catechin hydrate suppresses MCF-7 proliferation through TP53/Caspase-mediated apoptosis. J Exp Clin Cancer Res. 2010 Dec 17;29:167.

    [3]. Cheruku SP, et al. Catechin ameliorates doxorubicin-induced neuronal cytotoxicity in in vitro and episodic memory deficit in in vivo in Wistar rats. Cytotechnology. 2018 Feb;70(1):245-259.

Cell Assay
[2]

The Cell viability assay is performed to assess the toxicity of different concentrations of (+)-Catechin on MCF-7 cells. Briefly, MCF-7 cells (2×104 cells/well) are plated in 96-well plates and treated with 0 μg/mL (+)-Catechin and 160 μg/mL (+)-Catechin for 24 hours. Then, 40 μL of the Cell Titer Blue solution is directly added to the wells and incubated at 37°C for 6 hours. The fluorescence is recorded with a 560 nm/590 nm (excitation/emission) filter set using a microplate fluorescence reader, and the IC50 is calculated. Quadruplet samples are run for each concentration of (+)-Catechin in three independent experiments[2].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Administration
[3]

Rats[3]
Twelve weeks old, healthy male rats weighing 200 to 230 g are used in this study. Rats are divided into four experimental groups (n=9 each) for one vehicle and three groups of (+)-Catechin (three doses). The doses of (+)-Catechin are prepared at 50, 100, 200 mg/kg and administered orally for 7 days prior to and during the experimental trials. Episodic memory, the conscious memory of the past experiences is evaluated in this study[3].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

参考文献
  • [1]. Waffo-Téguo P, et al. Potential cancer-chemopreventive activities of wine stilbenoids and flavans extracted from grape (Vitis vinifera) cell cultures. Nutr Cancer. 2001;40(2):173-9.

    [2]. Alshatwi AA. Catechin hydrate suppresses MCF-7 proliferation through TP53/Caspase-mediated apoptosis. J Exp Clin Cancer Res. 2010 Dec 17;29:167.

    [3]. Cheruku SP, et al. Catechin ameliorates doxorubicin-induced neuronal cytotoxicity in in vitro and episodic memory deficit in in vivo in Wistar rats. Cytotechnology. 2018 Feb;70(1):245-259.

Rutin hydrate(Synonyms: Rutoside hydrate; Quercetin 3-O-rutinoside hydrate)

天然产物 糖类和糖苷 Saccharides and Glycosides

Rutin hydrate;(Synonyms: Rutoside hydrate; Quercetin 3-O-rutinoside hydrate) 纯度: ge;98.0%

Rutin (Rutoside) hydrate 是一种广泛存在于多种植物中的黄酮类化合物,具有抗炎、降糖、抗氧化、神经保护、肾脏保护、肝脏保护和降低 Aβ 低聚物活性等多种生物活性。Rutin hydrate 能穿过血脑屏障。Rutin hydrate 通过抑制细胞凋亡、线粒体功能紊乱和氧化应激抑制万古霉素诱导的肾小管细胞凋亡。

Rutin hydrate(Synonyms: Rutoside hydrate; Quercetin 3-O-rutinoside hydrate)

Rutin hydrate Chemical Structure

CAS No. : 207671-50-9

规格 价格 是否有货 数量
Free Sample (0.1-0.5 mg) ; Apply now ;
500 mg ¥400 In-stock
1 g ; 询价 ;
5 g ; 询价 ;

* Please select Quantity before adding items.

Rutin hydrate 相关产品

bull;相关化合物库:

  • Natural Product Library Plus
  • Drug Repurposing Compound Library Plus
  • FDA-Approved Drug Library Plus
  • Bioactive Compound Library Plus

生物活性

Rutin (Rutoside) hydrate is a flavonoid found in many plants and shows a wide range of biological activities including anti-inflammatory, antidiabetic, antioxidant, neuroprotective, nephroprotective, hepatoprotective and reducing Aβ oligomer activities. Rutin hydrate can cross the blood brain barrier. Rutin hydrate attenuates vancomycin-induced renal tubular cell apoptosis via suppression of apoptosis, mitochondrial dysfunction, and oxidative stress[1][2][3].

体内研究
(In Vivo)

Rutin hydrate ameliorates cadmium chloride-induced spatial memory loss and neural apoptosis in rats by enhancing levels of acetylcholine, inhibiting JNK and ERK1/2 activation and activating mTOR signaling[4].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Clinical Trial

分子量

740.26

Formula

C27H32O17

CAS 号

207671-50-9

中文名称

芸香苷水合物;紫皮甙水合物;维生素 P 水合物;芦丁水合物

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4deg;C, protect from light

*In solvent : -80deg;C, 6 months; -20deg;C, 1 month (protect from light)

溶解性数据
In Vitro:;

DMSO : 50 mg/mL (67.54 mM; Need ultrasonic)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 1.3509 mL 6.7544 mL 13.5088 mL
5 mM 0.2702 mL 1.3509 mL 2.7018 mL
10 mM 0.1351 mL 0.6754 mL 1.3509 mL

*

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month (protect from light)。-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。

In Vivo:

请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液,再依次添加助溶剂:

——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
分比是指该溶剂在您配制终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶

  • 1.

    请依序添加每种溶剂:;10% DMSO ;; 40% PEG300 ;; 5% Tween-80 ;; 45% saline

    Solubility: ≥ 2.5 mg/mL (3.38 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (3.38 mM,饱和度未知) 的澄清溶液。

    以 1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中,混合均匀;向上述体系中加入50 μL Tween-80,混合均匀;然后继续加入 450 μL生理盐水定容至 1 mL。

    将 0.9 g 氯化钠,完全溶解于 100 mL ddH₂O 中,得到澄清透明的生理盐水溶液

  • 2.

    请依序添加每种溶剂:;10% DMSO ;; 90% (20% SBE-β-CD in saline)

    Solubility: ≥ 2.5 mg/mL (3.38 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (3.38 mM,饱和度未知) 的澄清溶液。

    以 1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 900 μL 20% 的 SBE-β-CD 生理盐水水溶液中,混合均匀。

    将 2 g 磺丁基醚 β-环糊精加入 5 mL 生理盐水中,再用生理盐水定容至 10 mL,完全溶解,澄清透明
  • 3.

    请依序添加每种溶剂:;10% DMSO ;; 90% corn oil

    Solubility: ≥ 2.5 mg/mL (3.38 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (3.38 mM,饱和度未知) 的澄清溶液,此方案不适用于实验周期在半个月以上的实验。

    以 1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 900 μL玉米油中,混合均匀。

*以上所有助溶剂都可在 MCE 网站选购。
参考文献
  • [1]. Ghorbani A. Mechanisms of antidiabetic effects of flavonoid rutin. Biomed Pharmacother. 2017;96:305-312.

    [2]. Habtemariam S. Rutin as a Natural Therapy for Alzheimer’s Disease: Insights into its Mechanisms of Action. Curr Med Chem. 2016;23(9):860-873.

    [3]. Xu PX, et al. Rutin improves spatial memory in Alzheimer’s disease transgenic mice by reducing Aβ oligomer level and attenuating oxidative stress and neuroinflammation. Behav Brain Res. 2014;264:173-180.

    [4]. Abdel-Aleem GA, et al. Rutin hydrate ameliorates cadmium chloride-induced spatial memory loss and neural apoptosis in rats by enhancing levels of acetylcholine, inhibiting JNK and ERK1/2 activation and activating mTOR signalling. Arch Physiol Biochem. 2018;124(4):367-377.

Animal Administration
[1]

Rats[1]
(1) A control group receives of 0.01 g/mL carboxymethylcellulose (CMC) dissolved in distilled water; (2) α-tocopherol acetate treated group: control rats receive α-tocopherol (120 IU/rat) diluted in 0.1 mL of coconut oil; (3) Rutin hydrate treated control group (control + Rutin hydrate): control rats receive Rutin hydrate (100 mg/kg); (4) CdCl2 intoxicated group receives CdCl2 at a final dose of 5 mg/kg to induce neurotoxicity; (5) CdCl2 + Rutin hydrate treated group (CdCl2 + Rutin hydrate) receives CdCl2 (5 mg/kg) and receives a coincided dose of Rutin hydrate (100 mg/kg body weight); (6) CdCl2 + Rutin hydrate + α-tocopherol acetate-treated group receives CdCl2 (5 mg/kg) and receives concomitant dose of Rutin hydrate (100 mg/kg) in conjugation with α-tocopherol acetate (120 IU/rat) that is diluted in 0.1 mL of coconut oil. All treatments are given by orogastric gavage with a polyethylene catheter PE 190 daily for 30 days[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

参考文献
  • [1]. Ghorbani A. Mechanisms of antidiabetic effects of flavonoid rutin. Biomed Pharmacother. 2017;96:305-312.

    [2]. Habtemariam S. Rutin as a Natural Therapy for Alzheimer’s Disease: Insights into its Mechanisms of Action. Curr Med Chem. 2016;23(9):860-873.

    [3]. Xu PX, et al. Rutin improves spatial memory in Alzheimer’s disease transgenic mice by reducing Aβ oligomer level and attenuating oxidative stress and neuroinflammation. Behav Brain Res. 2014;264:173-180.

    [4]. Abdel-Aleem GA, et al. Rutin hydrate ameliorates cadmium chloride-induced spatial memory loss and neural apoptosis in rats by enhancing levels of acetylcholine, inhibiting JNK and ERK1/2 activation and activating mTOR signalling. Arch Physiol Biochem. 2018;124(4):367-377.

Oxypeucedanin hydrate(Synonyms: (+)-Oxypeucedanin hydrate)

天然产物 天然产物苯丙素类 Phenylpropanoids

Oxypeucedanin hydrate (Synonyms: (+)-Oxypeucedanin hydrate)

Oxypeucedanin hydrate ((+)-Oxypeucedanin hydrate) 是从 D. anethifolia 中分离出的一种天然产物。 Prangol 对成纤维细胞和母淋巴瘤细胞有轻微毒性。

Oxypeucedanin hydrate(Synonyms: (+)-Oxypeucedanin hydrate)

Oxypeucedanin hydrate Chemical Structure

CAS No. : 2643-85-8

规格 价格 是否有货 数量
5 mg ¥1300 In-stock
10 mg ¥2000 In-stock
25 mg ¥4100 In-stock
50 mg ¥6500 In-stock
100 mg   询价  
200 mg   询价  

* Please select Quantity before adding items.

Oxypeucedanin hydrate 相关产品

相关化合物库:

  • Natural Product Library Plus
  • Bioactive Compound Library Plus
  • Natural Product Library
  • Anti-Cancer Compound Library
  • Anti-Blood Cancer Compound Library

生物活性

Oxypeucedanin hydrate ((+)-Oxypeucedanin hydrate) is a natural product isolated from D. anethifolia. Prangol exhibits mild toxicity on fibroblasts and parental lymphoma cells[1].

分子量

304.29

Formula

C16H16O6

CAS 号

2643-85-8

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
参考文献
  • [1]. Mottaghipisheh J, et al. Antiproliferative and cytotoxic activities of furocoumarins of Ducrosia anethifolia. Pharm Biol. 2018 Dec;56(1):658-664.

(-)-Oxypeucedanin hydrate(Synonyms: (-)-Prangol)

天然产物 天然产物苯丙素类 Phenylpropanoids

(-)-Oxypeucedanin hydrate (Synonyms: (-)-Prangol)

(-)-Oxypeucedanin hydrate ((-)-Prangol) 是从 Ducrosia anethifolia 中分离得到的呋喃香豆素衍生物。

(-)-Oxypeucedanin hydrate(Synonyms: (-)-Prangol)

(-)-Oxypeucedanin hydrate Chemical Structure

CAS No. : 133164-11-1

规格 是否有货
5 mg 询价
10 mg 询价
25 mg 询价

* Please select Quantity before adding items.

生物活性

(-)-Oxypeucedanin hydrate ((-)-Prangol) is a derivative of furocoumarin isolated from Ducrosia anethifolia[1].

体外研究
(In Vitro)

D. anethifolia furocoumarin shows antiproliferative and cytotoxic activities[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

304.29

Formula

C16H16O6

CAS 号

133164-11-1

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

参考文献
  • [1]. Mottaghipisheh J, et al. Antiproliferative and cytotoxic activities of furocoumarins of Ducrosia anethifolia. Pharm Biol. 2018;56(1):658-664.

Osthol hydrate(Synonyms: 水合蛇床子素)

天然产物 天然产物苯丙素类 Phenylpropanoids

Osthol hydrate (Synonyms: 水合蛇床子素)

Osthol hydrate 是从 F. schottiana 中分离出的一种天然产物。

Osthol hydrate(Synonyms: 水合蛇床子素)

Osthol hydrate Chemical Structure

CAS No. : 69219-24-5

规格 是否有货
5 mg 询价
10 mg 询价
25 mg 询价

* Please select Quantity before adding items.

生物活性

Osthol hydrate is a natural product isolated from F. schottiana[1].

分子量

262.30

Formula

C15H18O4

CAS 号

69219-24-5

中文名称

水合蛇床子素

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

参考文献
  • [1]. Hollis, A., et al. The Chemical Constituents of Australian Flindersia Species. XIV. The Constituents of Flindersia pubescens Bail. And F. schottiana F. Muell. Australian Journal of Chemistry, 1961;14(1), 100.

4-Methylumbelliferyl-β-D-glucuronide hydrate(Synonyms: MUG)

4-Methylumbelliferyl-β-D-glucuronide hydrate;(Synonyms: MUG) 纯度: 99.98%

4-Methylumbelliferyl-β-D-glucuronide hydrate 是一种荧光底物 (λex=362 nm,λem=445 nm)。

4-Methylumbelliferyl-β-D-glucuronide hydrateamp;;(Synonyms: MUG)

4-Methylumbelliferyl-β-D-glucuronide hydrate Chemical Structure

CAS No. : 881005-91-0

规格 价格 是否有货 数量
Free Sample (0.1-0.5 mg) ; Apply now ;
10;mM;*;1 mL in DMSO ¥790 In-stock
25 mg ¥600 In-stock
50 mg ; 询价 ;
100 mg ; 询价 ;

* Please select Quantity before adding items.

4-Methylumbelliferyl-beta;-D-glucuronide hydrate 相关产品

bull;相关化合物库:

  • Bioactive Compound Library Plus
  • Glycoside Compound Library

生物活性

4-Methylumbelliferyl-β-D-glucuronide hydrate is a fluorogenic substrat (λex=362 nm , λem=445 nm).

体外研究
(In Vitro)

4-Methylumbelliferyl-β-D-glucuronide hydrate is a fluorogenic substrat with λex=362 nm and λem=445 nm. The half-saturation constants, Km, that are calculated for sewage samples are close to the Km values calculated based on experimental plots presented previously for freshwaters[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

370.31

Formula

C16H18O10

CAS 号

881005-91-0

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4deg;C, protect from light

*In solvent : -80deg;C, 6 months; -20deg;C, 1 month (protect from light)

溶解性数据
In Vitro:;

DMSO : 150 mg/mL (405.07 mM; Need ultrasonic)

H2O : 5.2 mg/mL (14.04 mM; Need ultrasonic and warming)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 2.7004 mL 13.5022 mL 27.0044 mL
5 mM 0.5401 mL 2.7004 mL 5.4009 mL
10 mM 0.2700 mL 1.3502 mL 2.7004 mL

*

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month (protect from light)。-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。

参考文献
  • [1]. George I, et al. Use of beta-D-galactosidase and beta-D-glucuronidase activities for quantitative detection of totaland fecal coliforms in wastewater. Can J Microbiol. 2001 Jul;47(7):670-5.

Kinase Assay
[1]

GLUase activity of E. coli cells is measured. Three millilitres of 4-Methylumbelliferyl-β-D-glucuronide hydrate (MUGlu) solution (55 mg of hydrated MUGlu and 20 mL of Triton X-100 in 50 mL of sterile water) is added to each flask (final concentration:165 mg/L). The incubation temperature is 44°C. One hundred microlitres of 2 M NaOH solution is added to each 2.9-mL aliquot to obtain a pH>10 before the fluorescence measurement[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

参考文献
  • [1]. George I, et al. Use of beta-D-galactosidase and beta-D-glucuronidase activities for quantitative detection of totaland fecal coliforms in wastewater. Can J Microbiol. 2001 Jul;47(7):670-5.

Glycyrrhizic Acid, Monoammonium Salt, n-Hydrate 品牌:Nagara Science


Glycyrrhizic Acid, Monoammonium Salt, n-Hydrate

品牌:Nagara Science
CAS No.:
储存条件:室温
纯度:>99%(HPLC)
产品编号

(生产商编号)

等级 规格 运输包装 零售价(RMB) 库存情况 参考值

NH080202

10 mg 咨询


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Acridine Orange hydrochloride hydrate 吖啶橙盐酸盐水合物 品牌:Chemodex


Acridine Orange hydrochloride hydrate

吖啶橙盐酸盐水合物

品牌:Chemodex
CAS No.:65-61-2 | 1704465-79-1
储存条件:+4°C
纯度:≥98% (HPLC)
产品编号

(生产商编号)

等级 规格 运输包装 零售价(RMB) 库存情况 参考值

CDX-A0005-G001

1 g 900.00


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* 零售价、促销产品折扣、运输费用、库存情况、产品及包装规格可能因各种原因有所变动,恕不另行通知,确切详情请联系上海金畔生物科技有限公司。

Acridine Orange hydrochloride hydrate 吖啶橙盐酸盐水合物 品牌:Chemodex


Acridine Orange hydrochloride hydrate

吖啶橙盐酸盐水合物

品牌:Chemodex
CAS No.:65-61-2 | 1704465-79-1
储存条件:+4°C
纯度:≥98% (HPLC)
产品编号

(生产商编号)

等级 规格 运输包装 零售价(RMB) 库存情况 参考值

CDX-A0005-G005

5 g 3,560.00


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AppliChem A1342.0100 L-Lysine 1-hydrate (DAB) pure, pharma grade 赖氨酸一水 39665-12-8 100 g

上海金畔生物科技有限公司提供AppliChem A1342.0100 L-Lysine 1-hydrate (DAB) pure, pharma grade 赖氨酸一水 39665-12-8 100 g,欢迎访问官网了解更多产品信息和订购

品牌 货号 产品名称 规格 价格

AppliChem A1342.0100 L-Lysine 1-hydrate (DAB) pure, pharma grade 赖氨酸一水 39665-12-8 100 g 3038.00

AppliChem A1340.1000 . . 1 kg 4408.00

AppliChem A1340.0100 . . 100 g 635.00

AppliChem A1325.9050 Medium 199 with Earle’s salts M199培养基 50 L 1598.00

AppliChem A1321.9010 Glasgow – MEM (BHK 21) Glasgow – MEM (BHK 21) 10 L 884.00

AppliChem A1288.9010 Pluronic® F-68 BioChemica 消泡剂 9003-11-6 10 kg 0.00

AppliChem A1288.0500 Pluronic® F-68 BioChemica 消泡剂 9003-11-6 500 g 2860.00

AppliChem A1284.0100 Tween® 20 – Solution 10 % peroxide-free 吐温20 9005-64-5 100 mL 2438.00

AppliChem A1278.0100 Thimerosal BioChemica 硫柳汞54-64-8 100 g 19084.00

AppliChem A1278.0025 Thimerosal BioChemica 硫柳汞54-64-8 25 g 4807.00

AppliChem A1272.0025 2-Nitrophenyl-ß-D-Galactopyranoside BioChemica 2-硝基苯基-β-D-吡喃半乳糖苷 生化级369-07-3 25 g 4927.00

AppliChem A1243.0005 NBT BioChemica 298-83-9 5 g 6857.00

AppliChem A1243.0001 NBT BioChemica 298-83-9 1 g 1881.00

AppliChem A1153.0500 Phenol equilibrated, stabilized Phenol equilibrated, stabilized 108-95-2 500 mL 2158.00

AppliChem A1152.0025 Ethidium Bromide – Solution 1 % BioChemica 溴化乙锭1239-45-8 25 mL 638.00

AppliChem A1149.9025 Sodium Chloride BioChemica 氯化钠7647-14-5 25 kg 4452.00

AppliChem A1148.0100 TEMED TEMED 110-18-9 100 mL 1484.00

AppliChem A1148.0025 TEMED TEMED 110-18-9 25 mL 718.00

AppliChem A1138.0250 α-Ketoglutaric Acid BioChemica α-酮戊二酸 328-50-7 250 g 7836.00

AppliChem A1126.1000 Cesium Chloride 99.9 % BioChemica 氯化铯 7647-17-8 1 kg 14336.00