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Merck
CN

855

萘酚 AS-MX 磷酸盐

别名:

Naphthol AS-MX phosphate

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关于此项目

经验公式(希尔记法):
C19H18NO5P
化学文摘社编号:
分子量:
371.32
UNSPSC Code:
12352204
NACRES:
NA.47
PubChem Substance ID:
EC Number:
216-480-1
Beilstein/REAXYS Number:
6664873
MDL number:
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form

solution

Quality Level

shelf life

Expiry date on the label.

IVD

for in vitro diagnostic use

concentration

0.25 % (w/v)

pH

8.6

application(s)

hematology
histology

storage temp.

2-8°C

SMILES string

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

Application

For use in Sigma Procedure 85 (kit numbers 85L1 and 85L2) for the demonstration of Alkaline Phosphatase, Leukocyte (LAP).
碱性磷酸酶组织化学显示的底物。

Other Notes

Naphthol AS-MX phosphate, 0.25% (w/v), buffered at pH 8.6, 25 C


pictograms

Corrosion

signalword

Warning

hcodes

Hazard Classifications

Met. Corr. 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

存储类别

10 - Combustible liquids

法规信息

监管及禁止进口产品

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Yongxin Ren et al.
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
Lei Shu et al.
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
J Espada et al.
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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