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N-Acetyl-D-galactosamine

N-Acetyl-D-galactosamine
N-Acetyl-D-galactosamine (GalNAc) 是一种源自半乳糖的末端必需氨基糖,在人体中形成​​ A 型血的抗原。
产品编号 T5885Cas号 14215-68-0
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纯度:99.49%
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N-Acetyl-D-galactosamine

产品编号 T5885别名 GalNAc, 2-乙酰胺基-2-脱氧-D-半乳糖Cas号 14215-68-0
N-Acetyl-D-galactosamine (GalNAc) 是一种源自半乳糖的末端必需氨基糖,在人体中形成​​ A 型血的抗原。
TargetMol的所有产品仅用作科学研究或药证申报,不能被用于人体,我们不向个人提供产品和服务。请您遵守承诺用途,不得违反法律法规规定用于任何其他用途。
规格价格库存数量
1 mg¥ 126现货
5 mg¥ 245现货
10 mg¥ 342现货
25 mg¥ 583现货
50 mg¥ 875现货
100 mg¥ 1,310现货
200 mg¥ 1,960现货
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"N-Acetyl-D-galactosamine"的相关化合物库

产品介绍

生物活性
产品描述
N-Acetyl-D-galactosamine (GalNAc) is a terminal essential amino sugar derived from galactose and forms the antigens of blood group A in humans.
体外活性
N-Acetyl-D-galactosamine (GalNAc or D-GalNAc) on the damage induced by SBA on the membrane permeability and tight junction proteins of piglet intestinal epithelium (IPEC-J2) cells. The IPEC-J2 cells were pre-cultured with 0, 0.125 × 10-4 , 0.25 × 10-4 , 0.5 × 10-4 , 1.0 × 10-4 and 2.0 × 10-4 mmol/L GalNAc at different time period (1, 2, 4 and 8 hr) before being exposed to 0.5 mg/ml SBA for 24 hr.Pre-incubation with GalNAc mitigates the mechanical barrier injury as reflected by a significant increase in trans-epithelial electric resistance (TEER) value and a decrease in alkaline phosphatase (ALP) activity in cell culture medium pre-treated with GalNAc before incubation with SBA as both indicate a reduction in cellular membrane permeability. In addition, mRNA levels of the tight junction proteins occludin and claudin-3 were lower in the SBA-treated groups without pre-treatment with GalNAc. The mRNA expression of occludin was reduced by 17.3% and claudin-3 by 42% (p < 0.01). Moreover, the corresponding protein expression levels were lowered by 17.8% and 43.5% (p < 0.05) respectively. However, in the GalNAc pre-treated groups, occludin and claudin-3 mRNAs were reduced by 1.6% (p > 0.05) and 2.7% (p < 0.01), respectively, while the corresponding proteins were reduced by 4.3% and 7.2% (p < 0.05). In conclusion, GalNAc may prevent the effect of SBA on membrane permeability and tight junction proteins on IPEC-J2s.
别名GalNAc, 2-乙酰胺基-2-脱氧-D-半乳糖
化学信息
分子量221.21
分子式C8H15NO6
CAS No.14215-68-0
储存&溶解度
存储Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
溶解度信息
H2O: 125 mg/mL (565.07 mM)
溶液配制表
H2O
1mg5mg10mg50mg
1 mM4.5206 mL22.6030 mL45.2059 mL226.0296 mL
5 mM0.9041 mL4.5206 mL9.0412 mL45.2059 mL
10 mM0.4521 mL2.2603 mL4.5206 mL22.6030 mL
20 mM0.2260 mL1.1301 mL2.2603 mL11.3015 mL
50 mM0.0904 mL0.4521 mL0.9041 mL4.5206 mL
100 mM0.0452 mL0.2260 mL0.4521 mL2.2603 mL

计算器

  • 摩尔浓度 计算器
  • 稀释 计算器
  • 配液 计算器
  • 分子量 计算器

体内实验配液计算器

请在以下方框中输入您的动物实验信息后点击计算,可以得到母液配置方法和体内配方的制备方法:
TargetMol | Animal experiments比如您的给药剂量是 10 mg/kg ,每只动物体重 20 g ,给药体积 100 μLTargetMol | Animal experiments 一共给药动物 10 只 ,您使用的配方为 5% TargetMol | reagent DMSO+ 30%PEG300+ 5%Tween 80 + 60% ddH2O. 那么您的工作液浓度为 2 mg/mL
母液配置方法: 2 mg 药物溶于 50 μLDMSOTargetMol | reagent ( 母液浓度为 40 mg/mL ), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。
体内配方的制备方法:50μLDMSOTargetMol | reagent 母液,添加 300 μLPEG300TargetMol | reagent 混匀澄清,再加 50μLTween 80, 混匀澄清,再加 600μLddH2OTargetMol | reagent 混匀澄清

以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。

1 请输入动物实验的基本信息
mg/kg
g
μL
2 请输入动物体内配方组成,不同的产品配方组成不同,如有配方需求,可先联系我们提供正确的体内配方。
% DMSO
%
%Tween 80
%ddH2O

剂量转换

对于不同动物的给药剂量换算,您也可以参考 更多

关键词

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