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Merck
CN

K2876

Keratanase from Pseudomonas sp.

lyophilized powder

别名:

Endo-β-galactosidase

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化学文摘社编号:
UNSPSC Code:
12352204
MDL number:
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form

lyophilized powder

packaging

vial of >10 units

storage temp.

−20°C

Other Notes

One unit will liberate 1.0 μmole of reducing sugar (measured as galactose) from keratan sulfate per hr at pH 7.4 at 37°C.

存储类别

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

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分析证书(COA)

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M N Fukuda
Current protocols in molecular biology, Chapter 17, Unit17-Unit17 (2008-02-12)
This overview covers the endo-beta-galactosidases; enzyme is capable of hydrolyzing a wide range of glycoconjugates. Endo-beta-galactosidases from numerous sources are discussed in terms of their substrate specificities and substrates, as well as their practical research applications.
William E B Johnson et al.
Arthritis and rheumatism, 46(10), 2658-2664 (2002-10-18)
To assess the effects of human intervertebral disc aggrecan on nerve growth and guidance, using in vitro techniques. Aggrecan extracted from human lumbar intervertebral discs was incorporated into tissue culture substrata for the culture of the human neuronal cell line
Alternative strategy for overcoming ABO incompatibility.
Takaaki Kobayashi et al.
Transplantation, 83(9), 1284-1286 (2007-05-15)
Yusuke Miki et al.
Xenotransplantation, 11(5), 444-451 (2004-08-12)
The presence of Galalpha1-3Galbeta1-4GlcNAc (alphaGal) in pigs is a formidable barrier for pig-to-primate xenotransplantation. We have reported that administration of recombinant endo-beta-galactosidase C (EndoGalC) removes alphaGal on porcine erythrocytes and kidneys. The present study examined the effects of EndoGalC gene
Takeomi Murata et al.
European journal of biochemistry, 270(18), 3709-3719 (2003-09-03)
Novel chromogenic substrates for endo-beta-galactosidase were designed on the basis of the structural features of keratan sulfate. Galbeta1-4GlcNAcbeta1-3Galbeta1-4GlcNAcbeta-pNP (2), which consists of two repeating units of N-acetyllactosamine, was synthesized enzymatically by consecutive additions of GlcNAc and Gal residues to p-nitrophenyl

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