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Butyrylcholinesterase (B7061)
inhibitors. J. Med. Chem., 46, 1-4 (2003).
3. Blong, R.M., et al., Tetramerization domain of
human butyrylcholinesterase is at the C-terminus.
Biochem. J., 327, 747-57 (1997).
4. Supplier Data
5. Masson
Data Sheet - C7512
inhibitors. J. Med. Chem., 46, 1-4 (2003).
4. Blong, R.M., et al., Tetramerization domain of
human butyrylcholinesterase is at the C-terminus.
Biochem. J., 327, 747-57 (1997).
5. Lee, J.C., and Harpst
Butyrylcholinesterase (C1057)
inhibitors. J. Med. Chem., 46, 1-4 (2003).
3. Blong, R.M., et al., Tetramerization domain of
human butyrylcholinesterase is at the C-terminus.
Biochem. J., 327, 747-57 (1997).
4. Lee, J.C., and Harpst
User Guide
44. (1993).
4. Kostic T, et al. Appl Microbiol Biotechnol.,
99(18): 7711–7722. (2015).
5. Azaiez H, et al. Hum Mutat., 24(4):305-11.
(2004).
6. Milte CM, et al. Eur J Nutr., 57(1):363-372.
Product Information Sheet - EMS0006
trifluoroethanol.
3. Add 20 L of the denaturing solution to the dried
sample.
4. Incubate at 57 C for 1 hour.
5. Alkylate the reduced sample by adding 5 L of
200 mM iodoacetamide
Data Sheet - G9888
kDa (SDS-PAGE)
Cofactor:
4
FAD
Optimal pH:
3
7.5–8.0
Optimal temperature:
2
37 C
KM:
4
2.3 mM
Activator:
2
Glycerol
Inhibitors:
4
benzylformic
Product Information Sheet - EMS0007
trifluoroethanol.
3. Add 20 L of the denaturing solution to the dried
sample.
4. Incubate at 57 C for 1 hour.
5. Alkylate the reduced sample by adding 5 L of
200 mM iodoacetamide
Product Information Sheet - EMS0004
trifluoroethanol.
3. Add 20 L of the denaturing solution to the dried
sample.
4. Incubate at 57 C for 1 hour.
5. Alkylate the reduced sample by adding 5 L of
200 mM iodoacetamide
Product Information Sheet - EMS0005
trifluoroethanol.
3. Add 20 L of the denaturing solution to the dried
sample.
4. Incubate at 57 C for 1 hour.
5. Alkylate the reduced sample by adding 5 L of
200 mM iodoacetamide
Product Information Sheet - A6338
yeast is a
tetramer consisting of subunits of approximately
57 kDa. The molecular weights of its monomer, dimer,
trimer, and tetramer are 57 kDa, 114 kDa, 171 kDa,
and 228 kDa, respectively. The monomers
Product Information Sheet - S9754
et al., Eur. J. Clin. Nutr., 57(2), 235-242
(2003).
7. Wang, P. et al., Cancer Prev. Res., 3(8), 985-993
(2010).
8. Henning, S.M. et al., Mol. Nutr. Food Res., 57(3),
483-493 (2013).
9. Tamae
Data Sheet - E2039
Denholm, E.M. et al., Eur. J. Pharmacol., 416(3),
213-221 (2001).
4. Aguiar, J.A.K. et al., Biotechnol. Appl. Biochem.,
37(2), 115-127 (2003).
RBG,DT,IG,GCY,MAM 07/16-1
2016 Sigma-Aldrich
Product Information Sheet - LI0601BC
stomacher.
2. Incubate at 37 °C ± 1 °C for 23 – 25 h.
3. After incubation, mix and inoculate 0.1 mL of culture in 10
mL full Fraser broth.
4. Incubate at 37 °C ± 1 °C for 22 – 26 h.
5.
Datasheet - P9120
Tarentino, A.L., et al., Biochemistry, 24,
4665-4671 (1985).
4. Tarentino, A.L., and Plummer, T.H., Methods in
Enzymology, 230, 44-57 (1994).
5. Trimble, R.B., and Tarentino, A.L., J. Biochem.
Product Information Sheet -T2859
.
3. Quality Control data.
4. The Merck Index, 12th, #9216, (1996).
5. Physicians’ Desk Reference, 47th ed., 1126,
(1993).
6. Beggs, W.H.J. Antimicrob. Chemother. 37, 841,
(1996).
7. Bottega
Product Information Sheet - SAE0202
Biochem., 73, 491-537 (2004).
6. Gendler, S.J., and Spicer, A.P., Annu. Rev.
Physiol., 57, 607-634 (1995).
7. Naughton, J. et al., Gut Microbes, 5(1), 48-52
(2014).
8. van Putten, J.P.M
Acetylcholinesterase (C0663)
days at 37 °C.
References
1. Massoulie, J., et al., Progress in Neurobiology, 41,
31-91 (1993).
2. Jbilo, O., et al., Toxicon, 32, 1445-1457 (1994).
3. Ott, P., et al., Eur. J. Biochem., 57, 469-
Data Sheet - SAB4200879
: E2005
(2018).
8. Taniguchi K., et al., Mol Carcinog., 57, 579-589
(2018).
9. Abdelhaleem M., Biochim Biophys Acta., 1704,
37-46 (2004).
Notice
We provide information and advice to our
Data Sheet - T4925
sample at 37 °C for
10-20 seconds in a water bath, then transfer the
sample to the cuvet preheated to 37 °C.
References
1. Luduena, R.F., et al., Current Opinion in Cell
Biology, 4
Spare parts for Mobius® FlexReady Solution with Smart Flexware® Assemblies For Chromatography and TFF
XV901
63
65
37
Applicable for
XV004
or XV005
20
38
53
20
37
66
21
61
40206460
62
56
80
55
53
65
DataSheet - E2039
Denholm, E.M. et al., Eur. J. Pharmacol., 416(3),
213-221 (2001).
4. Aguiar, J.A.K. et al., Biotechnol. Appl. Biochem.,
37(2), 115-127 (2003).
5. Ilham, Seffouh, "Analyse protéomique des
Product Information Sheet - I3750
Microbiol., 83, 120-126 (1997).
4. Bisson, J.W., and Cabelli, V.J., Membrane filter
enumeration method for Clostridium perfringens.
Appl. Environ. Microbiol., 37, 55-66 (1979).
5. Armon, R., and
DataSheet - P3752
Agriculturae Scandinavica,
Section B — Soil & Plant Science, 57(1), 65-73
(2007).
9. Smith, J.R. et al., Physiol. Genomics, 31(2),
37-363 (2007).
10. von Sperber, C. et al., Biogeosciences
MultiScreen Filter Plates with Ultracel®-10 Membrane
136 138 131 123
Cyto c 122 131 124 119 118 123 124 117
FBS 79 70 57 43 42 54 67 72
Human 64 55 43 33 33 43 54 61
30 ABS 68 57 45 37 37 47
Data Sheet - C8743
the product at –20 C.
References
1. Horinouchi, S. et al., Appl. Environ. Microbiol.,
57(5), 1386-1393 (1991).
TRITON is a trademark of The Dow Chemical Company
or an affiliated company
The Effective Use of Protein Kinase Inhibitors
MAPKAP-K1b 16 72 37 79 89 88 86 93 83 95 92 70 20 95 95 78 2 9 2
MAPKAP-K2 99 99 90 5 59 102 98 95 93 97 102 74 90 125 72 98 103 90
Suba-Seal Septa Set
9.5mm
53/24.0mm
49/22.0mm
41/19.0mm
21/21.0mm
57/25.5mm (C29/42)
29/14.0mm 25/12.5mm
(C14/20)
9/6.5mm
13/8.0mm
(C10/30)
37/17.5mm (C19/22)
45/20.5mm (C24/40)
33/16.0mm
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Data Sheet - C5740
Avoid repeated freezing and
thawing.
Procedure
4-Nitrophenol Hydroxylase Activity
A 0.5 ml reaction containing the following was
incubated at 37 °C for 30 minutes:
50 pmoles of cytochrome P450 isozyme
Data Sheet - A236
for central A3-
adenosine receptors. Mediation of behavioral depressant effects.” FEBS Lett. 336, 57-60 (1993).
Rev. 2/97
Product Information Sheet - O6881
inhibitor of xanthine
oxidase-catalyzed production of superoxide
radical. Biochem. Pharmacol., 37(2), 349-352
(1988).
4. Stryer, L., Biochemistry, 3rd ed., W.H. Freeman
(New York, NY: 1988), pp. 619-621.
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