CN
355-37-3
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关键词:'355-37-3'
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Data Sheet - 18723
solution
Concentration: 10 mM
pH: 7.5 +/-0.5
Spectroscopic Properties: λmax 255/355 nm; λexc 355 nm; λem 448 nm;
ε 23.3/5.8 L mmol
-1
cm
-1
(Tris-HCl
Data Sheet - SRP5073
PTPN12 (1-355), active (SRP5073) - Datasheet
PTPN12 (1-355), active, GST tagged, human
recombinant, expressed in E. coli cells
Catalog Number SRP5073
Storage Temperature –70 °C
Synonyms:
Data Sheet - 19511
solution
Concentration: 10 mM
pH: 7.5 +/-0.5
Spectroscopic Properties: λmax 255/355 nm; λexc 355 nm; λem 448 nm;
ε 23.3/5.8 L mmol
-1
cm
-1
(Tris-HCl
Data Sheet - 69234
solution
Concentration: 10 mM
pH: 7.5 +/-0.5
Spectroscopic Properties: λmax 252/355 nm; λexc 355 nm; λem 448 nm;
ε 22.6/5.7 L mmol
-1
cm
-1
(Tris-HCl
Data Sheet - 69244
solution
Concentration: 10 mM
pH: 7.5 +/-0.5
Spectroscopic Properties: λmax 252/355 nm; λexc 355 nm; λem 448 nm;
ε 22.6/5.7 L mmol
-1
cm
-1
(Tris-HCl
Data Sheet - I7642
Trinchieri, G., et al., Progress in Growth Factor
Research, 4, 355, (1992).
2. Merberg, D., et al., Immunol. Today, 13, 77 (1992).
3. Gearing, D., et al., Cell, 66, 9 (1991).
4. Schoenhaut, D.
BioTracker NTP-Transporter Molecule
cells with tricine buffer.
3. Incubate cells with a mixture (0.5 mL) of BioTracker NTP-
Transporter Molecule (20 µM) and Cy3-dUTP (20 µM) in the tricine
buffer for 3 min (37 °C; 5% CO2).
4. Remove staining
Data Sheet - Z4652
carcinogenesis.
Nutrition and Cancer, 57, 28-37 (2007).
2. Dreyer, D.L., and Bertelli, D.J., The structure of
Zapotin. Tetrahedron, 23, 4607-4612 (1967).
3. Cuendet, M., et al., Zapotin prevents mouse
Data Sheet - P3818
°C or after 3 days at 37 °C.
References
1. Lambert, N., and Freedman, R.B., Biochem. J., 213,
225-234 (1983).
2. Carmichael, D.F. et al., J. Biol. Chem., 252, 7163-
7167 (1977).
3. Land, S. et
Casein Kinase II from rat liver (C3460)
Traugh, J.A., Biochemistry, 30, 5586
(1991).
7. Khilko, S. et al., Protein Express. and Purif., 3, 355
(1992).
NDH/MAM 6/03
Sigma brand
Data Sheet - 84886
medium for isolation of dermatophytes from clinical materials. - Arch.
Dermat. Syphil., 67; 355-361
3. Georg L.K., Ajello D. and. Papageorge C., 1953, Use of cycloheximide in the selective isolation
Data Sheet - S0821
Cold Spring Harbor
Lab., (Cold Spring Harbor, NY), pp. 355-373
(1994).
2. Michaud, S., et al., Cell. Mol. Life Sci., 53, 104-
113 (1997).
3. Petersen, N.S., et al., Genetics, 92, 891-902
(1979)
Product Information Sheet - MAK237
to mix, and incubate in
the dark at 37 C for 1 hour.
7. Read samples in a fluorescence plate reader
(ex = 335–355 nm/ and em = 495–510 nm).
Background readings obtained
Monoclonal Anti-Cytochrome P450 2C6 (CYP2C6) Clone K1 (C0746)
J. Clin. Pharmacol., 52, 349-355
(2001).
6. Daniel, W.A., et al., Eur. Neuropsychopharmacol.,
16, 580-587 (2006).
7. Scollon, E.J., et al., Drug Metab. Dispos., 37, 221-
228 (2009).
GG,KAA,PHC
Data Sheet - 43314
presumptive bifidobacteria- colony count technique at
37°C, 2010.
2. S.N. Thitaram, G.R. Siragusa, A. Hinton Jr, Letters in Applied Microbiology, vol 41, 355-360, Bifidobacterium
selective isolation and enumeration
EX-CELL CHO Medium (C5467)
Biol. Animal, 35(4), 178-182
(1999).
4. Bjare, U., Serum-free culture. Pharmacol. Ther.,
53(3), 355-374 (1992).
Pluronic is a registered trademark of the BASF
Corporation.
LCM,MAM 04/05
EX-CELL CHO Medium (C1707)
Biol. Animal. 35(4), 178-182
(1999).
4. Bjare, U., Serum-free culture. Pharmacol. Ther.,
53(3), 355-374 (1992).
Precautions and Disclaimer MSDS is available upon
request or at sigma-aldrich.
Product Information Sheet - T1503
, in Diagnostic Cytogenetics (R.-D. Wegner,
ed.). Springer-Verlag (Berlin, Heidelberg), pp. 335-
355 (1999).
Trizma is a registered trademark of Sigma-Aldrich Co.,
LLC.
GCY,RXR,MAM 12/18-
Data Sheet - 73582
cap);
incubate for 8 min at 37 °C in a thermoshaker
2. Add 50 µL of Lysis Buffer C (red cap) and incubate for 8 min at 37°C and 1,400 rpm in the
thermoshaker
Data Sheet - 42875
cap);
incubate for 8 min at 37 °C in a thermoshaker
2. Add 50 µL of Lysis Buffer C (red cap) and incubate for 8 min at 37°C and 1,400 rpm in the
thermoshaker
Data Sheet - 86827
cap);
incubate for 8 min at 37 °C in a thermoshaker
2. Add 50 µL of Lysis Buffer C (red cap) and incubate for 8 min at 37°C and 1,400 rpm in the
thermoshaker
Data Sheet - 67289
cap);
incubate for 8 min at 37 °C in a thermoshaker
2. Add 50 µL of Lysis Buffer C (red cap) and incubate for 8 min at 37°C and 1,400 rpm in the
thermoshaker
Data Sheet - 49712
cap);
incubate for 8 min at 37 °C in a thermoshaker
2. Add 50 µL of Lysis Buffer C (red cap) and incubate for 8 min at 37°C and 1,400 rpm in the
thermoshaker
Data Sheet - 75724
cap);
incubate for 8 min at 37 °C in a thermoshaker
2. Add 50 µL of Lysis Buffer C (red cap) and incubate for 8 min at 37°C and 1,400 rpm in the
thermoshaker
Data Sheet - 76545
cap);
incubate for 8 min at 37 °C in a thermoshaker
2. Add 50 µL of Lysis Buffer C (red cap) and incubate for 8 min at 37°C and 1,400 rpm in the
thermoshaker
Data Sheet - 62915
Arizona cultures, AppI. Microbiol., 9, 478 (1961)
2. V. MöIIer, Acta Pathol. Microbiol. Scand., 355, 259 (1954)
3. W.H. Ewing, B.R. Davis, F.R.Edward, The decarboxylase reactions of Enterobacteriaceae and
Data Sheet - 89384
cap);
incubate for 8 min at 37 °C in a thermoshaker
2. Add 50 µL of Lysis Buffer C (red cap) and incubate for 8 min at 37°C and 1,400 rpm in the
thermoshaker
Data Sheet - 80065
cap);
incubate for 8 min at 37 °C in a thermoshaker
2. Add 50 µL of Lysis Buffer C (red cap) and incubate for 8 min at 37°C and 1,400 rpm in the
thermoshaker
Data Sheet - 77007
cap);
incubate for 8 min at 37 °C in a thermoshaker
2. Add 50 µL of Lysis Buffer C (red cap) and incubate for 8 min at 37°C and 1,400 rpm in the
thermoshaker
Data Sheet - 49417
cap);
incubate for 8 min at 37 °C in a thermoshaker
2. Add 50 µL of Lysis Buffer C (red cap) and incubate for 8 min at 37°C and 1,400 rpm in the
thermoshaker
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