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关键词:'329-98-6'
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Data Sheet - 78830
fluoride (Phenylmethylsulfonyl fluoride, α-Toluenesulfonyl fluoride, PMSF) CAS number: 329-98-6 Product Description: Appearance: White to faint yellow powder Molecular weight: 174.2 g/
Product Information - A6191
A6191 Page 2 of 2 11/16/98 - CKV ANTIPAIN HYDROCHLORIDE Sigma Prod. No. A6191 REFERENCES: 1. Data for Biochemical Research, 3rd Ed., eds. Dawson, R. et al., 328-329 (1987). 2. Suda, H. et al
Product Information - A8312
Biochemistry J., 221, 505-512 (1984). 5. Akparov, V.K. and Stepanov, V.M., J. Chromatography, 155, 329-336 (1978). 6. Mallia, A.K. et al., Analytical Letters, 14 (B8), 649-661 (1981). 7. Immobilized Affinity
Product Information Sheet - A8530
Biochemistry J., 221, 505-512 (1984). 5. Akparov, V.K. and Stepanov, V.M., J. Chromatography, 155, 329-336 (1978). 6. Mallia, A.K. et al., Analytical Letters, 14 (B8), 649-661 (1981). 7. Immobilized Affinity
Product Information Sheet - A4046
Biochemistry J., 221, 505-512 (1984). 5. Akparov, V.K. and Stepanov, V.M., J. Chromatography, 155, 329-336 (1978). 6. Mallia, A.K. et al., Analytical Letters, 14 (B8), 649-661 (1981). 7. Immobilized Affinity
Data Sheet - M7151
1978) 5. Sottrup-Jensen, L., et al., J. Biol. Chem., 259, 8318 (1984) 6. Shultze, N., Biochem. Z., 329, 490 (1958) 12/98 Sigma brand products are sold through Sigma-Aldrich, Inc. Sigma-Aldrich
Data Sheet - K2015
S.P., et al., J. Invest. Dermatol., 122, 812-819 (2004). 10. Winston, J.H., et al., J. Pain, 4, 329-337 (2003). EM,PHC 01/12-1 2011 Sigma-Aldrich Co. LLC. All rights reserved. SIGMA-ALDRICH is
Data Sheet - T5951
the optimal working dilutions by titration. References 1. Li, L., and Cohen, S.N., Cell, 85, 319-329 (1996). 2. Koonin, E.V., and Abagyan, R.A., Nature Genet., 16, 330-331 (1997). 3.
Data Sheet - T5826
the optimal working dilutions by titration. References 1. Li, L., and Cohen, S.N., Cell, 85, 319-329 (1996). 2. Koonin, E.V., and Abagyan, R.A., Nature Genet., 16, 330-331 (1997). 3. Watanabe, M
Data Sheet - T5701
the optimal working dilutions by titration. References 1. Li, L., and Cohen, S.N., Cell, 85, 319-329 (1996). 2. Koonin, E.V., and Abagyan, R.A., Nature Genet., 16, 330-331 (1997). 3.
Product Information Sheet - P7626
Phenylmethanesulfonyl Fluoride ≥98.5% (GC) P7626 Product Description CAS Registry Number: 329-98-6 Synonyms: PMSF, α-toluenesulfonyl fluoride, benzylsulfonylfluoride, phenylmethylsulfonyl
Product Information Sheet - O4511
Sato, Y., et al., Br. J. Pharmacol., 123, 97-105 (1998). 16. Easom, R. A., et al., Biochem. J., 329, 283-288 (1998). 17. Miller, C., et al., J. Cell Biochem., 69, 392-413 (1998). 18. Dinter, A
Product Information Sheet - O1506
Sato, Y., et al., Br. J. Pharmacol., 123, 97-105 (1998). 16. Easom, R. A., et al., Biochem. J., 329, 283-288 (1998). 17. Miller, C., et al., J. Cell Biochem., 69, 392-413 (1998). 18. Dinter, A
Product Information Sheet - SAE0094
tetramer 0.92 751 Non-engineered monomers 63 11 SAvPhire Monomeric Streptavidin 2.1 329 The size and monovalency of this product provide advantages over tetrameric streptavidin in
Data Sheet - B5183
Walters, D., The bistratenes: novel tools to study cell growth regulation. Progress Med. Chem. 1, 319-329 (1996) 4. Frey, M. R., et al., Stimulation of protein kinase C- dependent and -independent signaling
Kits and Reagents for Metabolic and Dietary Research
% 13C; 98 48,706-6 Thymine-d4 (methyl-d3,6-d1) 98 48,980-8 l-Tyrosine-2,3,5,6-d4 98 48,582-9 l-Tyrosine-2,6-d2 98 48,981-6 l-Tyrosine-3,5-d2 98 48,984-0 l-Tyrosine-3,3-d2 98 48,985-9
Data Sheet - M6159
8. Sottrup-Jensen, L., et al., J. Biol. Chem., 259, 8318 (1984). 9. Shultz, N., Biochem. Z., 329, 490 (1958). 10. Barrett, A.J., et. al., Biochem. J., 181, 401 (1979). 11. Barrett, A.J., Meth.
XP725 Antibody Number-Lot Number 071M4826
370 371 372 4.4 301 302 303 304 325 326 327 328 349 350 351 352 373 374 375 376 4.5 305 306 307 308 329 330 331 332 353 354 355 356 377 378 379 380 4.64. 309 310 311 312 333
Data Sheet - M6645
sodium bicarbonate] Osmolality 305 mOsm/kg H2O ± 5% [without sodium bicarbonate] Osmolality 329 mOsm/kg H2O ± 5% [with sodium bicarbonate] Endotoxin #1.0 EU/ml Amino Acid Analysis Analysis has
Data Sheet - L0650
JE: Am J Physiol 242: H645 1982. 20. Palek J, Liu SC: J Supramol Struct 10:79 1979. GJC 6/2/98 Sigma brand products are sold through Sigma-Aldrich, Inc. Sigma-Aldrich, Inc. warrants that
LABORATORY NOTEBOOK ISSUANCE PAGE
.9 98 20 .1 80 4. 00 26 26 .9 82 28 .0 85 30 .9 74 32 .0 6 35 .4 5 39 .9 48 69 .7 23 72 .6 3 74 .9 22 78 .9 6
Lab Notebook Guidelines
.9 98 20 .1 80 4. 00 26 26 .9 82 28 .0 85 30 .9 74 32 .0 6 35 .4 5 39 .9 48 69 .7 23 72 .6 3 74 .9 22 78 .9 6
Product Information Sheet - T0523
Second Edition, Volume 1 (K. Turksen, ed.). Methods in Molecular Biology, Vol. 329, Humana Press (Totowa, NJ), pp. 91-98 (2006). CMH,RXR,GCY,MAM 08/17-1 2017 Sigma-Aldrich Co. LLC
LABORATORY NOTEBOOK ISSUANCE PAGE
.9 98 20 .1 80 4. 00 26 26 .9 82 28 .0 85 30 .9 74 32 .0 6 35 .4 5 39 .9 48 69 .7 23 72 .6 3 74 .9 22 78 .9 6
LABORATORY NOTEBOOK ISSUANCE PAGE
.9 98 20 .1 80 4. 00 26 26 .9 82 28 .0 85 30 .9 74 32 .0 6 35 .4 5 39 .9 48 69 .7 23 72 .6 3 74 .9 22 78 .9 6
Reprint: Protein A Intermediate Wash Strategies
100 80 60 40 20 0 MAb 1 300 250 200 150 100 50 0 1,000 800 600 400 200 0 98 98 98 96 273 159 921 143 Figure 2: Effect of arginine on MAb yield and HCP removal
Protein A Intermediate Wash Strategies (Melissa Holstein, Kristen Cotoni and Nanying Bian) Bioprocess International February 2015
100 80 60 40 20 0 MAb 1 300 250 200 150 100 50 0 1,000 800 600 400 200 0 98 98 98 96 273 159 921 143 Figure 2: Effect of arginine on MAb yield and HCP removal
Glycobiology Brochure
(2-AB) ≥98% Fluorescently labels glycans containing a free reducing terminus. 10678 Anthranilic acid (2-AA) ≥99.0%, T Fluorescently labels glycans containing a free reducing terminus. 82393 6-Aza-2-thiothymine
Resins Brochure
tel. 314 534 4900 fax 314 652 0000 [87199-18-6] [5720-07-0] [66472-86-4] [32316-92-0] [87199-16-4] [52409-22-0] [10365-98-7] [98-80-6] [98546-51-1] [1679-18-1] [87199-17-5
Product Information Sheet - L3135
, M.M., J. Biol. Chem. 237, 329-333 (1962). 2. Nutter, L.J. and Privett, O.S., Lipids, 1, 258-262 (1966). 3. Panganamala, R.V. et al., Chem. Phys. Lipids, 6, 97-102 (1971). 4. Marsh
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