产品名称
Trizma® 盐酸溶液, pH 7.5, BioPerformance Certified, 1 M, suitable for cell culture
grade
BioPerformance Certified
Molecular Biology
form
solution
concentration
1 M
technique(s)
cell culture | mammalian: suitable
impurities
DNase, RNase, Protease, none detected
bioburden, tested
endotoxin, tested
≤5 ppm Heavy metals (as Pb)
pH
7.5
useful pH range
7.0-9.0
absorption
≤0.05 at 290 at 40%
Quality Level
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Application
Trizma®盐酸盐溶液用于吐温（Tween） tris缓冲盐溶液。 也用于制备链霉抗生物素蛋白-碱性磷酸酶，用于酶联免疫吸附测定（ELISA）。
General description
一系列 TRIZMA 碱和 TRIZMA HCl 的预混合溶液，为 Tris 缓冲液提供常用的 pH 值。不必混合或调节 pH 值。保证精确度 ± 0.1 个 pH 单位。
Legal Information
Trizma is a registered trademark of Merck KGaA, Darmstadt, Germany
存储类别
10 - Combustible liquids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
The development of a sensitive and specific ELISA for mouse eosinophil peroxidase: assessment of eosinophil degranulation ex vivo and in models of human disease
Ochkur SI, et al.
Journal of Immunological Methods, 375(1-2), 138-147 (2012)
Genomic maps of long noncoding RNA occupancy reveal principles of RNA-chromatin interactions.
Ci C Chu, Kun K Qu, Franklin L FL Zhong, Steven E SE Artandi, Howard Y HY Chang
Molecular Cell, 44, 667-678 null
Daniela Amann-Zalcenstein et al.
Nature immunology, 21(12), 1574-1584 (2020-10-21)
A classical view of blood cell development is that multipotent hematopoietic stem and progenitor cells (HSPCs) become lineage-restricted at defined stages. Lin-c-Kit+Sca-1+Flt3+ cells, termed lymphoid-primed multipotent progenitors (LMPPs), have lost megakaryocyte and erythroid potential but are heterogeneous in their fate.
An in vitro assay for sonothrombolysis based on the spectrophotometric measurement of clot thickness
Wang Z, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine, 36(4), 681-698 (2017)
Zuojun Wang et al.
Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine, 36(4), 681-698 (2017-02-06)
For improved thrombolysis therapy based on ultrasound irradiation, researchers and practitioners would strongly benefit from an easy and efficient in vitro assay system of thrombolysis activity involving irradiated ultrasound. For the present study, we designed a new in vitro sonothrombolysis
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