形式
solution
质量水平
保质期
Expiry date on the label.
IVD
for in vitro diagnostic use
浓度
0.25 % (w/v)
pH值(酸碱度)
8.6
应用
hematology
histology
储存温度
2-8°C
SMILES字符串
Cc1ccc(NC(=O)c2cc3ccccc3cc2OP(O)(O)=O)c(C)c1
InChI
1S/C19H18NO5P/c1-12-7-8-17(13(2)9-12)20-19(21)16-10-14-5-3-4-6-15(14)11-18(16)25-26(22,23)24/h3-11H,1-2H3,(H,20,21)(H2,22,23,24)
InChI key
IOMLBTHPCVDRHM-UHFFFAOYSA-N
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应用
碱性磷酸酶组织化学显示的底物。
For use in Sigma Procedure 85 (kit numbers 85L1 and 85L2) for the demonstration of Alkaline Phosphatase, Leukocyte (LAP).
组分
Naphthol AS-MX phosphate, 0.25% (w/v), buffered at pH 8.6, 25 C
警示用语:
Warning
危险声明
预防措施声明
危险分类
Met. Corr. 1
WGK
WGK 2
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
法规信息
监管及禁止进口产品
PloS one, 6(7), e23060-e23060 (2011-08-11)
Although the capacity of exogenous PTH1-34 to enhance the rate of bone repair is well established in animal models, our understanding of the mechanism(s) whereby PTH induces an anabolic response during skeletal repair remains limited. Furthermore it is unknown whether
Archives of ophthalmology (Chicago, Ill. : 1960), 127(8), 1029-1035 (2009-08-12)
To examine histopathologic and immunohistochemical features of human corneal buttons from patients who developed keratoglobus. Nine corneal buttons were obtained during penetrating keratoplasty from patients with keratoglobus. Histologic features were examined using hematoxylin-eosin-stained sections. Immunohistochemical staining for alpha1-proteinase inhibitor, Sp1
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 26(5), 1057-1071 (2011-05-05)
We have investigated, in neonates, whether the calcium-sensing receptor (CaR) mediates the effects of dietary calcium on bone turnover and/or modulates parathyroid hormone (PTH)-induced bone turnover. Wild-type (WT) pups and pups with targeted deletion of the Pth (Pth(-/-)) gene or
Biofabrication, 12(3), 035010-035010 (2020-04-08)
Acellular soft hydrogels are not ideal for hard tissue engineering given their poor mechanical stability, however, in combination with cellular components offer significant promise for tissue regeneration. Indeed, nanocomposite bioinks provide an attractive platform to deliver human bone marrow stromal
Histochemistry and cell biology, 108(6), 481-487 (1998-02-05)
The aim of this work was the development of a fluorescent microscopy technique to visualize acid phosphatase activity in living and pre-fixed cells. We have shown that a coupling azo dye method, using naphthol AS-MX phosphate (NP) as substrate and
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