赛多利斯Sartorius聚丙烯过滤杯 16A07-10-N 16A07-10-n


赛多利斯Sartorius聚丙烯过滤杯 16A07-10-N

赛多利斯Sartorius聚丙烯过滤杯 16A07-10-N 规格100ml 100个 赛多利斯Sartorius聚丙烯过滤杯 16A07-10-N 用于菌落计数,颗粒分析及显微镜检查

赛多利斯Sartorius聚丙烯 Microsart 100过滤杯   16A07-10-N

    Microsart 100过滤杯是一个100ml聚丙烯漏斗,带有20,50和100ml刻度标识。滤杯内径大,过滤速度快。zui优滤杯设计可彻底冲洗漏斗,无液体残留滤杯内。可适用于各种样品容量的过滤,在水,食品,饮料,制药,化妆品的日常检测中,能快速完成所要求的过滤任务。一个Sartorius Stedim Biotech的网格膜被放在一个不锈钢过滤器支座上,可以很轻松地将漏斗装在上面,对样品进行过滤。

规格:100ml     100个(分5个密封无菌包装)

材质:聚丙烯     

容量:100ml 刻度分为20,50和100ml

         250ml 刻度分为50,100,200和250ml

过滤器直径:47mm,预过滤器为40mm(仅用于颗粒分析)

过滤面积:13.2cm2  

zui高操作压力:真空

xiao毒:环氧乙烷

Lasalocid sodium(Synonyms: 拉沙洛西钠; Lasalocid-A sodium; Ionophore X-537A sodium; Antibiotic X-537A sodium)

上海金畔生物科技有限公司提供天然产物萜类及其苷类Terpenoids and Glycosides。

Lasalocid sodium (Synonyms: 拉沙洛西钠; Lasalocid-A sodium; Ionophore X-537A sodium; Antibiotic X-537A sodium) 纯度: ≥97.0%

Lasalocid sodium (Lasalocid-A sodium) 是一个抗菌剂。

Lasalocid sodium(Synonyms: 拉沙洛西钠; Lasalocid-A sodium; Ionophore X-537A sodium; Antibiotic X-537A sodium)

Lasalocid sodium Chemical Structure

CAS No. : 25999-20-6

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 ¥810 In-stock
5 mg ¥600 In-stock
10 mg ¥1000 In-stock
25 mg ¥1800 In-stock
50 mg ¥2700 In-stock
100 mg ¥3800 In-stock
200 mg   询价  
500 mg   询价  

* Please select Quantity before adding items.

Lasalocid sodium 相关产品

相关化合物库:

  • Natural Product Library Plus
  • Bioactive Compound Library Plus
  • Anti-Infection Compound Library
  • Natural Product Library
  • Anti-Cancer Compound Library
  • Autophagy Compound Library
  • Antibacterial Compound Library
  • Terpenoids Library
  • Phenols Library
  • Antibiotics Library
  • Microbial Metabolite Library

生物活性

Lasalocid sodium (Lasalocid-A sodium) treatment led to an increase in cell wall thickness, whilst the quantity and sugar composition of the cell wall remained unchanged in BY-2 cells. Lasalocid sodium (Lasalocid-A sodium) treatment enhances enzymatic saccharification efficiency in both BY-2 cells and Arabidopsis plants.

分子量

612.77

Formula

C34H53NaO8

CAS 号

25999-20-6

中文名称

拉沙洛西钠;拉沙里菌素钠;那塞罗钠

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, sealed storage, away from moisture

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

溶解性数据
In Vitro: 

DMSO : 100 mg/mL (163.19 mM; Need ultrasonic)

H2O : < 0.1 mg/mL (insoluble)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 1.6319 mL 8.1597 mL 16.3193 mL
5 mM 0.3264 mL 1.6319 mL 3.2639 mL
10 mM 0.1632 mL 0.8160 mL 1.6319 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 (sealed storage, away from moisture)。-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 (4.08 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (4.08 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% corn oil

    Solubility: ≥ 2.5 mg/mL (4.08 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (4.08 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]. Okubo-Kurihara E et al. Modification of plant cell wall structure accompanied by enhancement of saccharification efficiency using a chemical, lasalocid sodium. Sci Rep. 2016 Oct 3;6:34602.

Ferulic acid(Synonyms: Coniferic acid)

天然产物 天然产物苯丙素类 Phenylpropanoids

Ferulic acid (Synonyms: Coniferic acid) 纯度: 99.86%

Ferulic acid 是一种新型的成纤维细胞生长因子受体 1 (FGFR1) 抑制剂, 对于 FGFR1FGFR2IC50值分别为 3.78 和 12.5 μM。

Ferulic acid(Synonyms: Coniferic acid)

Ferulic acid Chemical Structure

CAS No. : 1135-24-6

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 ¥550 In-stock
100 mg ¥500 In-stock
1 g ¥650 In-stock
5 g ¥1800 In-stock
10 g   询价  
50 g   询价  

* Please select Quantity before adding items.

Ferulic acid 相关产品

相关化合物库:

  • Natural Product Library Plus
  • Drug Repurposing Compound Library Plus
  • FDA-Approved Drug Library Plus
  • FDA-Approved Drug Library Mini
  • Bioactive Compound Library Plus
  • Kinase Inhibitor Library
  • Metabolism/Protease Compound Library
  • Protein Tyrosine Kinase Compound Library
  • Natural Product Library
  • FDA-Approved Drug Library
  • Anti-Cancer Compound Library
  • Human Endogenous Metabolite Compound Library
  • Drug Repurposing Compound Library
  • Reprogramming Compound Library
  • Anti-COVID-19 Compound Library
  • NMPA-Approved Drug Library
  • Medicine Food Homology Compound Library
  • Phenols Library
  • Orally Active Compound Library
  • Traditional Chinese Medicine Monomer Library
  • FDA Approved & Pharmacopeial Drug Library
  • Anti-Lung Cancer Compound Library
  • Angiogenesis Related Compound Library
  • Food Additive Library
  • Food-Sourced Compound Library
  • Anti-Liver Cancer Compound Library
  • Rare Diseases Drug Library

生物活性

Ferulic acid is a novel fibroblast growth factor receptor 1 (FGFR1) inhibitor with IC50s of 3.78 and 12.5 μM for FGFR1 and FGFR2, respectively.

IC50 & Target[1]

FGFR1

3.78 μM (IC50)

FGFR2

12.5 μM (IC50)

Human Endogenous Metabolite

 

体外研究
(In Vitro)

Ferulic acid (FA) is a novel fibroblast growth factor receptor 1 (FGFR1) inhibitor with IC50s of 3.78 and 12.5 μM for FGFR1 and FGFR2, respectively. Ferulic acid exhibits great inhibitory activity on FGFR1 with an inhibitory rate of 92% at 1 µM. The proliferation of HUVEC stimulated by FGF1 is markedly decreased after Ferulic acid treatment ranging from 5 to 40 μM for 24 h. Ferulic acid does not exert significant cell viability up to 20 μM, but over 30 μM Ferulic acid exhibits a cytotoxic effect in HUVEC compare to the control. Ferulic acid inhibits FGF1-induced HUVEC migration and invasion in a dose-dependent manner. Ferulic acid markedly suppresses the FGF1-induced phosphorylation of PI3K and Akt. Ferulic acid treatments significantly inhibit MMP-2 and MMP-9 expression stimulated by FGF1[1].

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

体内研究
(In Vivo)

Treatment with Ferulic acid (FA) potently inhibits FGF1-induced neovascularization. It is found that intragastric administration of Ferulic acid markedly inhibits tumor volume and tumor weight, as compare to the counterparts treated with DMSO. Furthermore, Ferulic acid treatment is well tolerated, and there is no significant difference in weight between the vehicle group and the FA-treated groups[1]. Ferulic acid (0.01, 0.1, 1 or 10 mg/kg) given by oral route decreases significantly the immobility time in the forced swimming test (FST) and tail suspension test (TST), whereas produces no effect in the open-field test. Results demonstrate that the administration of Ferulic acid (0.001 mg/kg, p.o.) boosts the antidepressant-like effect of fluoxetine (5 mg/kg, p.o.) in the TST[2].

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

Clinical Trial

分子量

194.18

Formula

C10H10O4

CAS 号

1135-24-6

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 : 100 mg/mL (514.99 mM; Need ultrasonic)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 5.1499 mL 25.7493 mL 51.4986 mL
5 mM 1.0300 mL 5.1499 mL 10.2997 mL
10 mM 0.5150 mL 2.5749 mL 5.1499 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。-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 (12.87 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (12.87 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 (12.87 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (12.87 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 (12.87 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (12.87 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]. Yang GW, et al. Ferulic Acid Exerts Anti-Angiogenic and Anti-Tumor Activity by Targeting Fibroblast Growth Factor Receptor 1-Mediated Angiogenesis. Int J Mol Sci. 2015 Oct 12;16(10):24011-31.

    [2]. Zeni AL, et al. Ferulic acid exerts antidepressant-like effect in the tail suspension test in mice: evidence for the involvement of the serotonergic system. Eur J Pharmacol. 2012 Mar 15;679(1-3):68-74.

Cell Assay
[1]

HUVEC (5×104 cells/well) are plated onto a gelatinized 24-well culture plate and cultured in ECGS containing 15% FBS. HUVEC are treated with DMSO (0.1%) or different concentrations of Ferulic acid (FA) (0, 2.5, 5, 10, 20, 30, 40 μM) for 24 h. Cell viability is determined by the MTT assay. After 4 h of incubation, the absorbance is measured at 450 nm with a microplate reader. The results are calculated from six replicates of each experiment. Three independent experiments are performed[1].

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

Animal Administration
[2]

Male Swiss mice (30 to 40 g) are maintained at 21 to 23°C with free access to water and food, under a 12:12 h light/dark cycle (lights on at 07:00 h). All manipulations are carried out between, 9:00 and 16:00 h, with each animal used only once. In order to investigate the antidepressant-like effect of Ferulic acid, Ferulic acid is administered at a dose range of 0.001 to 10 mg/kg, by oral route (p.o.) 60 min before the forced swimming test (FST), tail suspension test (TST) or open-field test. The control animals receive appropriate vehicle[2].

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

参考文献
  • [1]. Yang GW, et al. Ferulic Acid Exerts Anti-Angiogenic and Anti-Tumor Activity by Targeting Fibroblast Growth Factor Receptor 1-Mediated Angiogenesis. Int J Mol Sci. 2015 Oct 12;16(10):24011-31.

    [2]. Zeni AL, et al. Ferulic acid exerts antidepressant-like effect in the tail suspension test in mice: evidence for the involvement of the serotonergic system. Eur J Pharmacol. 2012 Mar 15;679(1-3):68-74.

Indolokine A4

天然产物 黄酮类 Flavonoids

Indolokine A4 

Indolokine A4, 吲哚-3-丙酮酸 (I3P) 的分解代谢物, 是一种有效的 AhR 激动剂。

Indolokine A4

Indolokine A4 Chemical Structure

CAS No. : 1809317-07-4

规格 是否有货
100 mg   询价  
250 mg   询价  
500 mg   询价  

* Please select Quantity before adding items.

生物活性

Indolokine A4, a catabolite of indole-3-pyruvate (I3P), is a potent AhR agonist[1].

IC50 & Target

AhR[1]

分子量

274.30

Formula

C13H10N2O3S

CAS 号

1809317-07-4

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]. Gatsios A, et, al. Escherichia coli small molecule metabolism at the host-microorganism interface. Nat Chem Biol. 2021 Oct;17(10):1016-1026.

Lasalocid(Synonyms: Lasalocid-A; Ionophore X-537A; Antibiotic X-537A)

上海金畔生物科技有限公司提供天然产物萜类及其苷类Terpenoids and Glycosides。

Lasalocid (Synonyms: Lasalocid-A; Ionophore X-537A; Antibiotic X-537A) 纯度: ≥98.0%

Lasalocid (Lasalocid-A; Ionophore X-537A; Antibiotic X-537A) 是一种抗菌剂和抗球虫药, 用在饲料添加剂中。

Lasalocid(Synonyms: Lasalocid-A;  Ionophore X-537A;  Antibiotic X-537A)

Lasalocid Chemical Structure

CAS No. : 25999-31-9

规格 价格 是否有货 数量
10 mM * 1 mL in DMSO ¥780 In-stock
5 mg ¥600 In-stock
10 mg ¥1000 In-stock
25 mg ¥1800 In-stock
50 mg ¥2700 In-stock
100 mg ¥3900 In-stock
200 mg   询价  
500 mg   询价  

* Please select Quantity before adding items.

Lasalocid 相关产品

相关化合物库:

  • Natural Product Library Plus
  • Bioactive Compound Library Plus
  • Anti-Infection Compound Library
  • Natural Product Library
  • Anti-Cancer Compound Library
  • Autophagy Compound Library
  • Antibacterial Compound Library
  • Terpenoids Library
  • Phenols Library
  • Antibiotics Library
  • Microbial Metabolite Library

生物活性

Lasalocid (Lasalocid-A; Ionophore X-537A; Antibiotic X-537A) is an antibacterial agent and a coccidiostat, used in the feed additives

分子量

590.79

Formula

C34H54O8

CAS 号

25999-31-9

中文名称

拉沙洛西;拉沙里菌素;那塞罗

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 : 100 mg/mL (169.26 mM; Need ultrasonic)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 1.6926 mL 8.4632 mL 16.9265 mL
5 mM 0.3385 mL 1.6926 mL 3.3853 mL
10 mM 0.1693 mL 0.8463 mL 1.6926 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。-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 (4.23 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (4.23 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% corn oil

    Solubility: ≥ 2.5 mg/mL (4.23 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (4.23 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]. Chen M, et al. Effect of monensin and lasalocid-sodium on the growth of methanogenic and rumen saccharolytic bacteria. Appl Environ Microbiol. 1979 Jul;38(1):72-7.

荧光染料Br-Mmc(Synonyms: 4-Bromomethyl-7-methoxycoumarin)

荧光染料Dye Reagents Br-Mmc;(Synonyms: 4-Bromomethyl-7-methoxycoumarin)

Br-Mmc (4-Bromomethyl-7-methoxycoumarin) 通常用作荧光标记,用于测定含有羧基的化合物。Br-Mmc 可通过 TLC 或 HPLC 测定脂肪酸含量。

Br-Mmc(Synonyms: 4-Bromomethyl-7-methoxycoumarin)

Br-Mmc Chemical Structure

CAS No. : 35231-44-8

规格 是否有货
100 mg ; 询价 ;
250 mg ; 询价 ;
500 mg ; 询价 ;

* Please select Quantity before adding items.

Br-Mmc 相关产品

bull;相关化合物库:

  • Fragment Library

生物活性

Br-Mmc (4-Bromomethyl-7-methoxycoumarin) is often used as fluorescent label for the determination of compounds possessing a carboxylic group. Br-Mmc is used for the determination fatty acids by TLC or HPLC[1][2][3].

分子量

269.09

Formula

C11H9BrO3

CAS 号

35231-44-8

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder -20deg;C 3 years
4deg;C 2 years
In solvent -80deg;C 6 months
-20deg;C 1 month
参考文献
  • [1]. Wolf JH, et al. 4-Bromomethyl-7-methoxycoumarin and analogues as derivatization agents for high-performance liquid chromatography determinations: a review. J Pharm Biomed Anal. 1992 Feb-Mar;10(2-3):99-107.

    [2]. Wang K, et al. Derivatization of 5-fluorouracil with 4-bromomethyl-7-methoxycoumarin for determination by liquid chromatography-mass spectrometry. J Am Soc Mass Spectrom. 1998 Sep;9(9):970-6.

    [3]. Hagen V, et al. Synthesis, photochemistry and application of (7-methoxycoumarin-4-yl)methyl-caged 8-bromoadenosine cyclic 3′,5′-monophosphate and 8-bromoguanosine cyclic 3′,5′-monophosphate photolyzed in the nanosecond time region. J Photochem Photobiol B. 1999 Nov-Dec;53(1-3):91-102.

Procyanidin A1(Synonyms: 原花青素 A1; Proanthocyanidin A1)

天然产物 黄酮类 Flavonoids

Procyanidin A1 (Synonyms: 原花青素 A1; Proanthocyanidin A1) 纯度: 99.19%

原花青素 A1 (Proanthocyanidin A1) 是一种原花青素二聚体,抑制蛋白激酶 C 激活下游脱粒或 RBL-213 细胞内部储存的 Ca2+ 流入。原花青素 A1 具有抗过敏作用。

Procyanidin A1(Synonyms: 原花青素 A1; Proanthocyanidin A1)

Procyanidin A1 Chemical Structure

CAS No. : 103883-03-0

规格 价格 是否有货 数量
10 mM * 1 mL in DMSO ¥5707 In-stock
1 mg ¥1500 In-stock
5 mg ¥4500 In-stock
10 mg ¥6800 In-stock
50 mg   询价  
100 mg   询价  

* Please select Quantity before adding items.

Procyanidin A1 相关产品

相关化合物库:

  • Natural Product Library Plus
  • Bioactive Compound Library Plus
  • Epigenetics Compound Library
  • Immunology/Inflammation Compound Library
  • Kinase Inhibitor Library
  • TGF-beta/Smad Compound Library
  • Natural Product Library
  • Reprogramming Compound Library
  • Oxygen Sensing Compound Library
  • Phenols Library
  • Cytoskeleton Compound Library
  • Traditional Chinese Medicine Monomer Library
  • Flavonoids Library
  • Food-Sourced Compound Library

生物活性

Procyanidin A1 (Proanthocyanidin A1) is a procyanidin dimer, which inhibits degranulation downstream of protein kinase C activation or Ca2+ influx from an internal store in RBL-213 cells. Procyanidin A1 has antiallergic effects[1].

体内研究
(In Vivo)

Procyanidin A1 suppress serum IgE and IgG1 levels in mice-immunized with ovalbumin[2].

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

分子量

576.50

Formula

C30H24O12

CAS 号

103883-03-0

中文名称

原花青素 A1

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, protect from light

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

溶解性数据
In Vitro: 

DMSO : 100 mg/mL (173.46 mM; Need ultrasonic)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 1.7346 mL 8.6730 mL 17.3461 mL
5 mM 0.3469 mL 1.7346 mL 3.4692 mL
10 mM 0.1735 mL 0.8673 mL 1.7346 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 (4.34 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (4.34 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 (4.34 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (4.34 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 (4.34 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (4.34 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]. Tomochika K, et al. Effects of peanut-skin procyanidin A1 on degranulation of RBL-2H3 cells. Biosci Biotechnol Biochem. 2011;75(9):1644-8.

    [2]. Takano F, et al. Aqueous extract of peanut skin and its main constituent procyanidin A1 suppress serum IgE and IgG1 levels in mice-immunized with ovalbumin. Biol Pharm Bull. 2007 May;30(5):922-7.

Bacoside A3(Synonyms: 苦艾素A3;假马齿苋皂素A3)

上海金畔生物科技有限公司提供天然产物萜类及其苷类Terpenoids and Glycosides。

Bacoside A3 (Synonyms: 苦艾素A3;假马齿苋皂素A3) 纯度: 98.47%

Bacoside A3 是一种三萜皂苷,是 Bacopa monnieri 的主要活性成分之一。Bacoside A3 具有神经保护活性。

Bacoside A3(Synonyms: 苦艾素A3;假马齿苋皂素A3)

Bacoside A3 Chemical Structure

CAS No. : 157408-08-7

规格 价格 是否有货 数量
1 mg ¥2000 In-stock
5 mg ¥5000 In-stock
10 mg   询价  
50 mg   询价  

* Please select Quantity before adding items.

Bacoside A3 相关产品

相关化合物库:

  • Natural Product Library Plus
  • Bioactive Compound Library Plus
  • Natural Product Library
  • Glycoside Compound Library
  • Terpenoids Library
  • Neuroprotective Compound Library

生物活性

Bacoside A3, a triterpenoid saponin, is one of the major active constituents in Bacopa monnieri. Bacoside A3 has neuroprotective activity[1].

分子量

929.10

Formula

C47H76O18

CAS 号

157408-08-7

中文名称

苦艾素A3;假马齿苋皂素A3

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, protect from light

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

参考文献
  • [1]. Vini C Sekhar, et al. Insights Into the Molecular Aspects of Neuroprotective Bacoside A and Bacopaside I. Curr Neuropharmacol. 2019;17(5):438-446.

N-Acetylneuraminic acid(Synonyms: 唾液酸; NANA; Lactaminic acid)

天然产物 糖类和糖苷 Saccharides and Glycosides

N-Acetylneuraminic acid;(Synonyms: 唾液酸; NANA; Lactaminic acid) 纯度: ge;98.0%

N-Acetylneuraminic酸是一个在细胞膜的糖蛋白和哺乳细胞神经节甘脂的糖脂上普遍存在的唾液酸单糖,在神经传递, 白细胞血管渗出,病毒或细菌感染起着生物作用。

N-Acetylneuraminic acid(Synonyms: 唾液酸; NANA;  Lactaminic acid)

N-Acetylneuraminic acid Chemical Structure

CAS No. : 131-48-6

规格 价格 是否有货 数量
Free Sample (0.1-0.5 mg) ; Apply now ;
10;mM;*;1 mL in Water ¥550 In-stock
100 mg ¥500 In-stock
1 g ¥700 In-stock
5 g ; 询价 ;
10 g ; 询价 ;

* Please select Quantity before adding items.

N-Acetylneuraminic acid 相关产品

bull;相关化合物库:

  • Natural Product Library Plus
  • Clinical Compound Library Plus
  • Bioactive Compound Library Plus
  • Anti-Infection Compound Library
  • Metabolism/Protease Compound Library
  • Natural Product Library
  • Clinical Compound Library
  • Antiviral Compound Library
  • Human Endogenous Metabolite Compound Library
  • Anti-Cardiovascular Disease Compound Library
  • FDA Approved amp; Pharmacopeial Drug Library
  • Gut Microbial Metabolite Library
  • Microbial Metabolite Library
  • Food-Sourced Compound Library

生物活性

N-Acetylneuraminic acid is a nine-carbon, sialic acid monosaccharide commonly found in glycoproteins on cell membranes and in glycolipids such as gangliosides in mammalian cells. Studies suggest that N-Acetylneuraminic acid is useful biologically in neurotransmission, leukocyte extravasation, viral or bacterial infections and carbohydrate-protein recognition.

IC50 Target

Human Endogenous Metabolite

;

分子量

309.27

Formula

C11H19NO9

CAS 号

131-48-6

中文名称

唾液酸;N-乙酰神经氨酸;醋纽拉酸;N-乙酰涎酸;氧-唾液酸;N-乙酰-神经氨 (糖) 酸

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

-20deg;C, stored under nitrogen

*In solvent : -80deg;C, 6 months; -20deg;C, 1 month (stored under nitrogen)

溶解性数据
In Vitro:;

H2O : ≥ 100 mg/mL (323.34 mM)

* “≥” means soluble, but saturation unknown.

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 3.2334 mL 16.1671 mL 32.3342 mL
5 mM 0.6467 mL 3.2334 mL 6.4668 mL
10 mM 0.3233 mL 1.6167 mL 3.2334 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 (stored under nitrogen)。-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]. Bondioli L et al. PLGA nanoparticles surface decorated with the sialic acid, N-acetylneuraminic acid. Biomaterials. 2010 Apr;31(12):3395-403.

    [2]. Kiefel MJ, et al. Synthesis and biological evaluation of N-acetylneuraminic acid-based rotavirus inhibitors. J Med Chem. 1996 Mar 15;39(6):1314-20.

荧光染料Coelenterazine hcp

荧光染料Dye Reagents Coelenterazine hcp;

Coelenterazine hcp 是 Coelenterazine 类似物。Coelenterazine hcp 对 Ca2+具有高度敏感性。Coelenterazine hcp 适用于监测细胞内钙2+

Coelenterazine hcp

Coelenterazine hcp Chemical Structure

CAS No. : 123437-32-1

规格 是否有货
100 mg ; 询价 ;
250 mg ; 询价 ;
500 mg ; 询价 ;

* Please select Quantity before adding items.

生物活性

Coelenterazine hcp is a Coelenterazine analogue. Coelenterazine hcp shows high sensitivity to Ca2+. Coelenterazine hcp is suited for monitoring intracellular Ca2+[1].

分子量

399.48

Formula

C25H25N3O2

CAS 号

123437-32-1

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]. Jiang T, et al. Lighting up bioluminescence with coelenterazine: strategies and applications. Photochem Photobiol Sci. 2016;15(4):466-480.