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- 文献和实验
- 技术资料
- 保存条件:
常温
- 保质期:
根据瓶身LOT号查询
- 英文名:
Trizma® base
- 库存:
有现货
- 供应商:
浙江羽翔生物科技有限公司
- CAS号:
77-86-1
- 规格:
5KG
属性
质量水平
300
描述
aminopeptidase substrate
检测方案
≥99.9% (titration)
形式
crystalline
储存条件
dry at room temperature
技术
ELISA: suitable
protein extraction: suitable
颜色
white
pH值(酸碱度)
10.5-12
有效pH范围
7-9
pKa (25 °C)
8.1
bp
219-220 °C/10 mmHg (lit.)
mp
167-172 °C (lit.)
溶解性
methanol: soluble 26 mg/mL at 25 °C
ethylene glycol: soluble 79.1 mg/mL at 25 °C
water: soluble (678 g/l at 20 °C)
吸光度
≤0.05 at 290 nm at 40%
适用性
suitable for Western blot
suitable for electrophoresis
应用
cell analysis
diagnostic assay manufacturing
life science and biopharma
SMILES字符串
NC(CO)(CO)CO
InChI
1S/C4H11NO3/c5-4(1-6,2-7)3-8/h6-8H,1-3,5H2
InChI key
LENZDBCJOHFCAS-UHFFFAOYSA-N
一般描述
Tris 碱可能会用作碱度标准品、独立地作为缓冲剂以及作为混合缓冲剂配方(包括 Tris-EDTA (TE) 缓冲液、TAE 缓冲液、TBE 缓冲液等)中的关键成分。其属性包括纯度、基本稳定性和相对不吸湿性,使其成为实验室环境中的可靠选择。在这些环境中,Tris 碱对于制备与生物体液相容的缓冲液是必不可少的,并可作为标准 pH 溶液。它有利于各种实验室程序,例如乳酸脱氢酶测定、原位杂交和从细胞中提取蛋白质。Tris 碱的多功能性扩展到细胞生物学、生物化学和蛋白质研究,对涉及细胞膜通透性和缓冲液制备的研究做出了重大贡献。
应用
- 用作H缓冲液(细胞解离缓冲液)组分
- 洗涤和浸润双夹心ELISA免疫酶技术测定反应孔
- 用作重悬提取并烘干的蛋白质样品的测定缓冲液
- 制备用于稳定蛋白质的Tris-HCl缓冲液
- 用作从块茎中提取类胡萝卜素的缓冲液
- 用作蛋白质印迹前蛋白提取过程的样品缓冲液组分
- 用作十二烷基硫酸钠聚丙烯酰an凝胶电泳 (SDS-PAGE)的样品缓冲液组分
- 制备用于磷酸钙(CaP)吸附测定的模拟体液(SBF)
- 用作在不锈钢(SS)基材上沉积聚多巴胺(PDA)的缓冲液
特点和优势
- 在 pH 值 7 - 9 范围内有效缓冲,pKa 8.1 (25 °C)
- 经过测试,确认重金属污染水平较低,确保适合各种应用
- 可用于细胞生物学和生化研究
其他说明
对于精确的应用,使用经过精心校准的 pH 计和玻璃/gan汞组合电极。
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文献和实验Cross talk between the response regulators PhoB and TctD allows for the integration of diverse environmental signals in Pseudomonas aeruginosa.
Two-component systems (TCS) serve as stimulus-response coupling mechanisms to allow organisms to adapt to a variety of environmental conditions. The opportunistic pathogen Pseudomonas aeruginosa encodes for more than 100 TCS components. To avoid unwanted cross-talk, signaling cascades are very specific, with one sensor talking to its cognate response regulator (RR). However, cross-regulation may provide means to integrate different environmental stimuli into a harmonized output response. By applying a split luciferase complementation assay, we identified a functional interaction of two RRs of the OmpR/PhoB subfamily, namely PhoB and TctD in P. aeruginosa. Transcriptional profiling, ChIP-seq analysis and a global motif scan uncovered the regulons of the two RRs as well as a quadripartite binding motif in six promoter regions. Phosphate limitation resulted in PhoB-dependent expression of the downstream genes, whereas the presence of TctD counteracted this activation. Thus, the integration of two important environmental signals e.g. phosphate availability and the carbon source are achieved by a titration of the relative amounts of two phosphorylated RRs that inversely regulate a common subset of genes. In conclusion, our results on the PhoB and TctD mediated two-component signal transduction pathways exemplify how P. aeruginosa may exploit cross-regulation to adapt bacterial behavior to complex environments.
Tween-20 Amresco 0777 Bromphenol Blue Amresco 0449 DTT Amresco 0281 Trizma base Sigma T1503 Protease inhibitor cocktail Roche 04693116001 Non-fat milk Erie yili
QUALITATIVE ANALYSIS OF DNA FRAGMENTATION BY AGAROSE GEL ELECTROPHORESIS
, dihydrate E-5134 Sigma TRIZMA base (Tris) T-1503 Sigma Triton X-100 115291A BioRad Sodium Chloride S-9888 Sigma Isopropyl alcohol 412421 Carlo Erba Ethanol 1170 Riedel-deHaen Lauryl sulphate, sodium salt (SDS) L-4390
5%6%7.5%`10%12%15%water6.86.335.744.43.82.5450% glycerol0.10.110.110.120.20.31.5 M Tris, pH 8.833333310% SDS0.120.120.120.120.120.12Acrylamide22.4344.86TEMED (µl)55555510% persulfate (µl)353535353535Sample Buffers:Dehydrating Solution 30% Methanol
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