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Merck

420290

IPTG, Hemidioxane Adduct

A free-flowing, hygroscopic carbohydrate that induces expression of the lac operon of E. coli by allosterically interacting with the repressor molecule.

Synonym(s):

IPTG, Hemidioxane Adduct, Isopropyl-β-D-thiogalactopyranoside

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About This Item

Empirical Formula (Hill Notation):
C9H18O5S · 0.5C4H8O2
CAS Number:
Molecular Weight:
282.35
NACRES:
NA.25
UNSPSC Code:
12352201
MDL number:
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Product Name

IPTG, Hemidioxane Adduct, A free-flowing, hygroscopic carbohydrate that induces expression of the lac operon of E. coli by allosterically interacting with the repressor molecule.

InChI

1S/C9H18O5S/c1-4(2)15-9-8(13)7(12)6(11)5(3-10)14-9/h4-13H,3H2,1-2H3/t5-,6+,7+,8-,9+/m1/s1

InChI key

BPHPUYQFMNQIOC-NXRLNHOXSA-N

assay

≥98% (HPLC)

form

solid

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze
desiccated (hygroscopic)

impurities

15.0% dioxane

color

white to off-white

solubility

water: 1%
ethanol: soluble

shipped in

ambient

storage temp.

2-8°C

Quality Level

Disclaimer

Toxicity: Carcinogenic / Teratogenic (D)

General description

A free flowing carbohydrate that induces expression of the lac operon of E. coli by allosterically interacting with the repressor molecule. Inducer of β-D-galactosidase.
A free-flowing, hygroscopic carbohydrate that induces expression of the lac operon of E. coli by allosterically interacting with the repressor molecule. Inducer of β-D-galactosidase. This preparation contains 15% dioxane.

Other Notes

Mathur, A., et al. 2000. Cardiovasc. Res. 46, 126.
Chanda, B., and Mathew, M.K. 1999. Biochim Biophys. Acta 1416, 92.
Dedov, V.N., and Roufogalis, B.D. 1999. FEBS Lett. 456, 171.
Polla, B.S., et al. 1996. Proc. Natl. Acad. Sci. USA 93, 6458.
White, R.J., et al. 1996. J. Neurosci. 16, 5688.
Ankacrona, M., et al. 1995. Neuron 15, 961.
Reers, M., et al. 1995. Methods Enzymol. 260, 406.
Ravanello, M.P., and Kruby, D.E. 1994. J. Virol.68, 6401.
Schmitz, M.L., and Baeurerle, P.A. 1994. Biotechniques17, 714.
Cossarizza, A., et al. 1993. Biochem. Biophys. Res. Commun. 197, 40.
Lama, J., et al. 1992. Gene117, 185.
Zhang, Y., and Moss, B. 1991. Proc. Natl. Acad. Sci. USA88, 1511.
Rodriquez, J.F., and Smith, G.L. 1990. Nucleic Acids Res.18, 5347.
Date, T., et al. 1988. Biochem. Biophys. Res. Commun.151, 598.
Lee, S.G., et al. 1988. Biochemistry27, 2983.
Cho, S., et al. 1985. Biochem. Biophys. Res. Commun.128, 1268.

Preparation Note

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 6 months at -20°C.

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificates of Analysis (COA)

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