288-32-4

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Showing 1-30 of 70 results for "288-32-4" within Technical Documents

restriction endonuclease: pH dependence and proton transfers in catalysis. J. Mol. Biol., 288(1), 105-116 (1999). 4. Colet, J. M., et al., Dynamic evaluation of the hepatic uptake and clearance of manganese

Quick Start Guide-mPAGE® Color Protein Standard

123 87 61 50 32 26 15 10 kDa 275 151 121 86 61 50 32 26 15 10 kDa 288 165 129 91 63 50 33 27 15 10 kDa 291 156 126 91 63 49

Data Sheet - 56749

56749 / 56748 Imidazole (Glyoxaline, 1,3-Diaza-2,4-cyclopentadiene) CAS number: 288-32-4 Product Description: Molecular Formula: C3H4N2 Molecular Weight: 68.08 g/mol pH: 9.5

Product Information Sheet - I0125

Information Sheet Imidazole Catalog Number I0125 Store at Room Temperature CAS RN: 288-32-4 Molecular Formula: C3H4N2 Molecular Weight: 68.08 pKa: 7.1 1 Melting Point: 90-91 °C2

Product Information Sheet - I0250

Information Sheet Imidazole Catalog Number I0250 Store at Room Temperature CAS RN: 288-32-4 Molecular Formula: C3H4N2 Molecular Weight: 68.08 pKa: 7.1 Melting Point: 90-91 °C2 Product

Data Sheet - 56748

56749 / 56748 Imidazole (Glyoxaline, 1,3-Diaza-2,4-cyclopentadiene) CAS number: 288-32-4 Product Description: Molecular Formula: C3H4N2 Molecular Weight: 68.08 g/mol pH: 9.5

Product Information Sheet - I5513

Imidazole, for molecular biology Catalog Number I5513 Store at Room Temperature CAS RN: 288-32-4 Molecular Formula: C3H4N2 Molecular Weight: 68.08 pKa: 7.1 Melting Point: 90-91 °C2 Product

Product Information Sheet - R4018

chain. Science, 179(70), 285-288 (1973). 4. Litt, M., A simple procedure for the purification of yeast phenylalanine transfer RNA. Biochem. Biophys. Res. Commun., 32(3), 507-511 (1968). 5. Schmidt

TB038VM pET-22b(+) Vector Map

2202 2397 2788 4360 4519 4878 MspI 32 MspA1I 10 84 267 1144 1714 1807 2806 2925 3557 3802 4743 MwoI 39 NarI 4 437 458 572 1754 NciI 12 NcoI 1 220 NdeI 1 288 NgoAIV 5 231 424 2012 2172 5352 NlaIII

TB037VM pET-20b(+) Vector Map

2865 NcoI 1 220 NdeI 1 288 NgoAIV 2 231 3575 NlaIII 15 NlaIV 15 NotI 1 166 NspI 3 783 1075 1442 Pfl1108I 1 2349 PleI 6 367 1332 1817 2320 3409 3417 Psp5II 2 402 444 Psp1406I 4 763 2557 2930 3259 PstI

TB259VM pETBlue™-2 Vector Map

2 709 1800 AlwNI 1 2854 ApaLI 2 2406 2949 ApoI 4 307 614 1509 1520 AscI 1 320 AvaI 2 288 431 AvaII 5 641 1877 2099 3425 3513 AvrII 1 597 BamHI 1 301 BanI 4 341 1285 1687 3545 BanII 2 297 1255 BbsI 3 423

Periodic table Poster

[Ar] 3d104s24p1 32 72.64 938.25 2833 2.02Ge 4 [Ar] 3d104s24p2 33 74.922 subl. 616 subl. 616 2.20As –3, 3, 5 [Ar] 3d104s24p3 34 78.96 221 685 2.48Se –2, 4, 6

Product Information Sheet - M1753

spectrometry of conjugated benzo[a]pyrene metabolites. Rapid Commun. Mass Spectrom., 3(9), 286-288 (1989). 10. Tengvall, P., et al., Complement activation by 3- mercapto-1,2-propanediol immobilized

Product Information Sheet - M6145

spectrometry of conjugated benzo[a]pyrene metabolites. Rapid Commun. Mass Spectrom., 3(9), 286-288 (1989). 10. Tengvall, P., et al., Complement activation by 3- mercapto-1,2-propanediol immobilized

Data Sheet - M1689

Gαq-Dependent Activation of Mitogen-Activated Protein Kinase Kinase 4/c-Jun N-Terminal Kinase Cascade. Biochem. Biophys. Res. Commun., 288, 1087-1094 (2001). LLK 8/23/01 Sigma brand

MultiScreen®96-well Ultrafiltration Plates with Ultracel®-10K Membrane

Buffer 288 290 291 292 295 291 290 288 CmT 272 269 265 261 262 264 266 271 FBS 80 64 47 32 33 48 66 83 30 min BSA 256 260 264 262 266 264

Product Information Sheet - N4505

, 82(2), 288-299 (1959). 3. Enzymatic Analysis. A Practical Guide, Passonneau, J.V., and Lowry, O.H., Humana Press (Totowa, NJ:1993), pp. 9-10. 4. Methods of Enzymatic Analysis, Vol. 4, Bergmeyer

OMPT: Subtype selective lysophosphatidicacid (LPA3) receptor agonist

2 , 20 04 O rd er : 1- 80 0- 32 5- 30 10 Te ch ni ca l S er vi ce : 1- 80 0- 32 5-

Data Sheet - N8129

Biophys., 82(2), 288-299 (1959). 3. Passonneau, J.V., and Lowry, O.H., Enzymatic Analysis. A Practical Guide. Humana Press (Totowa, NJ), pp. 9-10 (1993). 4. Bergmeyer et al., Vol. 4, pp. 2066-2072

LABORATORY NOTEBOOK ISSUANCE PAGE

100 0 — 1 78.54 32 0.81 2.57 288 1.505 p–Xylene 0.866 138 12 27 0.65 2.27 290 1.495 Also, "nd a pdf "le on the Solvents Table

LABORATORY NOTEBOOK ISSUANCE PAGE

100 0 — 1 78.54 32 0.81 2.57 288 1.505 p–Xylene 0.866 138 12 27 0.65 2.27 290 1.495 Also, "nd a pdf "le on the Solvents Table

LABORATORY NOTEBOOK ISSUANCE PAGE

100 0 — 1 78.54 32 0.81 2.57 288 1.505 p–Xylene 0.866 138 12 27 0.65 2.27 290 1.495 Also, "nd a pdf "le on the Solvents Table

Product Information Sheet - N1161

82(2), 288-299 (1959). 3. Passonneau, J.V., and Lowry, O.H., Enzymatic Analysis. A Practical Guide. Humana Press (Totowa, NJ), pp. 9-10 (1993). 4. Bergmeyer et al., Vol. 4, pp. 2066-2072

Product Information Sheet - R0395

powder2 The E1 %, 1 cm (maximum wavelength, 95% ethanol) is: 417 (267 nm); 541 (277 nm); 416 (288 nm).1 Molecular Formula: C51H79NO13 Molecular Weight: 914.2 Rapamycin is extracted from a microbial

Quality Control Range Sheet- B6062-101A and B6062-201A

Control 2 343 – 713 pg/mL Control 2 1661 – 3450 pg/mL Lymphotactin Control 1 288 – 599 pg/mL TRAIL Control 1 92 – 191 pg/mL

Data Sheet - A6606

Cellular dehydration and immunoglobulin binding in senescent neonatal erythrocytes. Pediatr. Res., 23, 288-92 (1988). 12. Matovik, L.M., et al., Drug-induced endocytosis of neonatal erythrocytes. Blood

XP725 Antibody Number-Lot Number 071M4826

e-f g-h a-b c-d e-f g-h a-b c-d e-f g-h a-b c-d e-f g-h 1.1 1 2 3 4 25 26 27 28 49 50 51 52 73 74 75 76 1.2 5 6 7 8 29 30 31 32

Periodic table A4

3d104s24p1 32 72.64 938.25 2833 2.02 Ge 4 [Ar] 3d104s24p2 33 74.922 subl. 616 subl. 616 2.20 As –3, 3, 5 [Ar] 3d104s24p3 34 78.96 221 685 2.48

Chirosolv Brochure

and Rapid Chiral Resolution with ChiroSolv® Kits 0 5 10 15 20 25 16 32 48 96 144 192 240 288 336 384 No. of Resolving Agents Manual screening Screening with

Celltransmissions Newsletter

Vo l 2 0, N o. 1, 2 00 4 O rd er : 1- 80 0- 32 5- 30 10 Te ch ni ca l S er vi ce :

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