CN
510-13-4
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关键词:'510-13-4'
显示 1-30 共 129 条结果 关于 "510-13-4" 范围 技术文档
Product Information Sheet - E2642
1989).
2. Bayer, E.A., and Wilchek, M., J. Chromatogr.,
510, 3-11 (1990).
3. Wilchek, M., Protein Sci., 13(11), 3066-3070
(2004).
4. O'Connor, E. et al., J Immunol Methods.,
229(1-2), 155
Sterikon plus Bioindicator: Incubation Time Validation
Guidance for Industry and FDA Staff —
Biological Indicator (BI) Premarket Notification [510(k)]
Submission” (October 4, 2007).
The validation study (performed by Quality Control
Darmstadt, Germany) described
Data Sheet - SAB4200725
Wu ZA., et al,. J Cell Biol., 113, 465-83 (1991).
12. Edmond V., et al ., EMBO J., 30, 510-23 (2011).
13. McFarlane M., et al., J Virol., 89, 5276-87
(2015).
14. Jang SW., et
Product Information Sheet - NTSV
Synonyms: N-(3-triethylammoniumpropyl)-4-(4-
(dibutylamino)styryl)pyridinium dibromide); FM1-43
Molecular Formula: C30H49Br2N3
Molecular Weight: 611.55
λex = 510 nm; λem = 625 nm in methanol
λex = 480
Product Information Sheet - C6880
M. and Watanabe, S., Eur. J. Pharmacol.,
318, 267 (1996).
8. Watson, G.B., et al., Brain Res., 510, 158-160
(1990).
9. Flood, J.F., et al., Eur. J. Pharmacol., 221, 249
(1992).
10. Schuster
Product Information Sheet - C7670
M. and Watanabe, S., Eur. J. Pharmacol.,
318, 267 (1996).
8. Watson, G.B., et al., Brain Res., 510, 158-160
(1990).
9. Flood, J.F., et al., Eur. J. Pharmacol., 221, 249
(1992).
10. Schuster
Product Information Sheet - C3909
M. and Watanabe, S., Eur. J. Pharmacol.,
318, 267 (1996).
8. Watson, G.B., et al., Brain Res., 510, 158-160
(1990).
9. Flood, J.F., et al., Eur. J. Pharmacol., 221, 249
(1992).
10. Schuster
Data Sheet - A2543
.
3. Geiger, B., and Singer, S.J., Cell, 16, 213-222
(1979).
4. Maruyama, K., and S. Ebashi, J., Biochem.
(Tokyo), 58, 13-19 (1965).
5. Geiger, B., et al., Proc. Natl. Acad. Sci. USA,
76
Data Sheet - 92322
Food Protect. Vol. 50, 8, 658-661 (1987)
3. J.M. De Smedt et al., Int. J. Food Micro. 13, 301-308 (1991)
4. R. Holbrook, J.M. Anderson, A.C. Baird-Parker, L.M. Dodds, D. Sawhney, S.H. Struchbury, D
Data Sheet - R8407
et al., J. Biol. Chem., 275, 29138-29146
(2000).
7. Caswell, P.T. et al., Develop. Cell, 13, 496-510
(2007).
VS,ST,TD,KAA,PHC,MAM 04/19-1
2019 Sigma-Aldrich Co. LLC. All rights
Data Sheet - C7117
4. Skowyra, D., et al., Cell, 91, 209-219 (1997).
5. Kamura, T., et al., Science, 284, 657-661 (1999).
6. Maniatis, T., Genes Dev., 13, 505-510 (1999).
7. Winston, J.T., et al., Genes Dev., 13, 270
Data Sheet - SAB4200220
et al., J. Biol. Chem., 275, 29138-29146
(2000).
7. Caswell, P.T., et al., Develop. Cell, 13, 496-510
(2007).
VS,ST,TD,KAA,PHC,MAM 07/19-1
2019 Sigma-Aldrich Co. LLC. All rights
Product Information Sheet - E2642
1989).
2. Bayer, E.A., and Wilchek, M., J. Chromatogr.,
510, 3-11 (1990).
3. Wilchek, M., Protein Sci., 13(11), 3066-3070
(2004).
4. O'Connor, E. et al., J Immunol Methods., 229(1-
2), 155-160
Data Sheet - E2513
-12 (1989).
2. Bayer,E.A., and Wilchek, M., J. Chromatogr.,
510, 3-11 (1990).
3. Wilchek, M., Protein Sci., 13, 3066-70 (2004).
4. O'Connor, E. et al., J. Immunol. Methods, 229,
155-60 (1999)
Data Sheet - SAB4200325
et al., J. Biol. Chem., 275, 29138-29146
(2000).
7. Caswell, P.T., et al., Develop. Cell, 13, 496-510
(2007).
ST,TD,KAA,PHC 09/11-1
Data Sheet - R8532
et al., J. Biol. Chem., 275, 29138-29146
(2000).
7. Caswell, P.T. et al., Develop. Cell, 13, 496-510
(2007).
VS,ST,TD,KAA,PHC,MAM 04/19-1
2019 Sigma-Aldrich Co. LLC. All rights
Data Sheet - 30020
agonist at the glycine modulatory site of the
NMDA receptor expressed in Xenopus oocytes Brain Res. 510, 158-160 (1990)
9. Flood, J.F., et al., Eur. J. Pharmacol., 221, 249 (1992).
10. Schuster, G.M. and
5-Bromo-4-chloro-3-indolyl beta-D-glucuronide sodium salt (B8049)
Chromogenic
Substrate 5-Bromo-4-Chloro-3-Indolyl β-D-
Glucuronide (X-Gluc) for Enumerating Escherichia
coli in 24 h from Ground Beef. J. Food. Prot., 53,
508-510 (1990).
4. Bomineni, V.R., et al., Transformation
Product Information sheet - B8174
Ley, A., J. Clin. Microbiol.,
27(4), 778-779 (1989).
4. Restaino, L. et al., J. Food. Prot., 53(6), 508-510
(1990).
5. Bomineni, V.R. et al., Plant Cell Rep., 13(1),
17-23 (1993).
6. Ellis
Product Information sheet - B8049
Ley, A., J. Clin. Microbiol.,
27(4), 778-779 (1989).
4. Restaino, L. et al., J. Food. Prot., 53(6), 508-510
(1990).
5. Bomineni, V.R. et al., Plant Cell Rep., 13(1),
17-23 (1993).
6. Ellis
Quality Control Ranges: Human Cytokine/ Chemokine/Growth Factor Magnetic Bead Panel A
Control 1 86 - 179 pg/mL MCP-1 Control1 111 - 231 pg/ml
Control 2 441 - 917 pg/mL Control 2 510 - 1059 pg/ml
http://www.lincoresearch.com/
5-Bromo-4-chloro-3-indolyl beta-D-glucuronide sodium salt (B8174)
Chromogenic
Substrate 5-Bromo-4-Chloro-3-Indolyl β-D-
Glucuronide (X-Gluc) for Enumerating Escherichia
coli in 24 h from Ground Beef. J. Food. Prot., 53,
508-510 (1990).
4. Bomineni, V.R., et al., Transformation
Data Sheet - SAB4200361
et al., J. Biol. Chem., 275, 29138-29146
(2000).
7. Caswell, P.T., et al., Develop. Cell, 13, 496-510
(2007).
DS,PHC 04/16-1
Product Information Sheet - E7637
(absorption) at 510 nm, Em at 590 nm.11
Ex (absorption) at 482 nm (blue-green), Em at 616 nm
(red-orange).12 The fluorescence yield of EtBr increases
as solvent polarity decreases.13
Ethidium bromide
Product Information Sheet - E1385
(absorption) at 510 nm, Em at 590 nm.11
Ex (absorption) at 482 nm (blue-green), Em at 616 nm
(red-orange).12 The fluorescence yield of EtBr increases
as solvent polarity decreases.13
Ethidium bromide
Data Sheet - P9489
Natl. Acad. Sci. USA, 93,
11173 (1996).
7. Kwon, Y.T., and Tsai, L-H., J. Comp. Neurol., 395,
510 (1998).
8. Chae, T., et al., Neuron, 18, 29 (1997).
9. Ohshima, T., et al., Proc. Natl. Acad. Sci.
Product Information Sheet - T0523
(1984).
17. Young, S.P., et al., Biochem. J., 219(2), 505-510
(1984).
18. Stein, B.S., and Sussman, H.H., J. Biol. Chem.,
258(4), 2668-2673 (1983).
19. Sawyer, S.T., and Krantz, S.B., J.
LuminiCell Tracker¿ 670- Cell Labeling Kit
E
Day 5
Day 7
Day 9
Day 13
Unlabeled
Day 0
Day 0
Day 5
Day 7
Day 9, 13
Product Information Sheet-LYSISO1
assessed
using the dye Neutral Red. The absorbance maximum
of the Neutral Red dye shifts from 460 nm to 510 nm
in the acidic pH conditions found in the lysosome. The
Neutral Red dye will concentrate in
Product Information Sheet - T2252
Biochem. J., 219(2), 505-510 (1984).
18. Stein, B.S., and Sussman, H.H., Peptide mapping
of the human transferrin receptor in normal and
transformed cells. J. Biol. Chem., 258(4), 2668-
2673 (1983).
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