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Key Documents

S7313

Sigma-Aldrich

S-Gal® sodium salt

reagent for selection of recombinant bacterial clones

Synonyme(s) :

3,4-Cyclohexeneoesculetin-B-D-galactopyranoside sodium salt

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About This Item

Formule empirique (notation de Hill):
C19H21O9Na
Poids moléculaire :
416.35
Numéro MDL:
Code UNSPSC :
12352200
Nomenclature NACRES :
NA.85

Qualité

for molecular biology

Stérilité

non-sterile

Pureté

≥95% (HPLC)

Forme

powder

IVD

not for in vitro diagnostic use

Solubilité

H2O: 100 mg/mL

Adéquation

suitable for β-galactosidase test

Température de stockage

room temp

Description générale

S-Gal® (sodium salt) is an autoclavable, water-soluble, chromogenic substrate for β-galactosidase, used to determine the presence or absence of a cloned DNA insert in bacteria growing on agar plates. S-gal® is designed to replace X-Gal in blue-white selection of recombinant bacterial colonies with the lac+ phenotype.

Application

S-Gal, sodium salt is a patented water-soluble, autoclavable chromogenic substrate for β-galactosidase that is designed to replace X-Gal in blue-white selection of recombinant bacterial colonies with the lac+ phenotype.

Caractéristiques et avantages

  • More intense color contrast than X-gal
  • Water-soluble and autoclavable for easiest use
  • Excellent for use in automated colony counters
  • No need to make stock solutions
When S-Gal is cleaved by β-galactosidase, the resulting product will chelate ferric ion to create a black, insoluble precipitate. Lac+ colonies grown in the presence of S-Gal and ferric ion turn an intense black color, allowing for easy differentiation between lac+ and lac- colonies. S-Gal, Sodium salt is water soluble, eliminating the need for solvents such as dimethyl formamide. S-Gal is also autoclavable and can be added to your medium of choice prior to autoclaving. S-Gal is not light sensitive and does not require any protection from light sources.

Autres remarques

More water soluble version, soluble >50 mg/mL.
The ferric or Fe3+ ion is required for color development and must be added to any S-Gal®
formulation. A medium prepared with S-Gal® is moderately dark due to the presence of ferric ammonium citrate. This darker background often provides enhanced contrast for automated colony counting or isolation.

Attention

For black color development to occur, ferric ion must be present. Although we recommend ferric ammonium citrate (500 mg/L of media), other ferric compounds can be used to provide this requirement, depending upon your particular system.

Principe

When S-Gal® is cleaved by ß-galactosidase, the resulting product will chelate ferric ion to create a black, insoluble precipitate. Lac+ colonies grown in the presence of S-Gal® and ferric ion turn an intense black color, allowing for easy differentiation between lac+ and lac- colonies.

Liaison

Ferric Ammonium Citrate (F5879), LB Agar (L2897), IPTG (Isopropyl β-D-thiogalactopyranoside, I6758), Ampicillin (A2804), Kanamycin (K0879), Chloramphenicol (C7795), Tetracycline (T8032)

Reconstitution

Add to agar media pre-autoclaving at a recommended concentration of 300 mg S-Gal/L of media, along with 500 mg/L Ferric Ammonium Citrate (F5879). Stock solutions of S-Gal can be made by dissolving at 50 mg/mL in deionized water, sterile-filtering and storing at -20 °C.
Stock solutions of S-Gal® (sodium salt) can be made by dissolving 50mg/ml in water, dimethyl formamide (DMF) or DMSO. Filter sterilize and store at -20C. Add S-gal® (300 mg/L from stock solution or powder) and Ferric Ammonium Citrate (500mg/L) to agar media prior to autoclaving.

Informations légales

S-GAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)


Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

Winfried Hense et al.
PLoS biology, 5(10), e273-e273 (2007-10-12)
Genes with male- and testis-enriched expression are under-represented on the Drosophila melanogaster X chromosome. There is also an excess of retrotransposed genes, many of which are expressed in testis, that have "escaped" the X chromosome and moved to the autosomes.
Weina Cui et al.
Magnetic resonance in medicine, 64(1), 65-71 (2010-06-24)
Reporter genes and associated enzyme activity are becoming increasingly significant for research in vivo. The lacZ gene and beta-galactosidase (beta-gal) expression have long been exploited as reporters of biologic manipulation at the molecular level, and a noninvasive detection strategy based
S-Gal?, A novel 1H MRI reporter for ?-galactosidase?
Weina Cui
Magnesium Research (2010)

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