S-Gal™: An Autoclavable Dye for Color Selection of Cloned DNA Inserts
Blue/white selection is the standard method for detecting a cloned DNA fragment. In the absence of an insert, uninterrupted expression of the vector-encodeda-complement of β-galactosidase (β-gal), results in the hydrolysis of X-gal (5-bromo-4-chloro-3-indolyl β-d-galactoside) and the subsequent blue...
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| Format: | Article |
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Taylor & Francis Group
2001-05-01
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| Series: | BioTechniques |
| Online Access: | https://www.future-science.com/doi/10.2144/01305pf01 |
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| author | Ken Heuermann Jennifer Cosgrove |
| author_facet | Ken Heuermann Jennifer Cosgrove |
| author_sort | Ken Heuermann |
| collection | DOAJ |
| description | Blue/white selection is the standard method for detecting a cloned DNA fragment. In the absence of an insert, uninterrupted expression of the vector-encodeda-complement of β-galactosidase (β-gal), results in the hydrolysis of X-gal (5-bromo-4-chloro-3-indolyl β-d-galactoside) and the subsequent blue staining of the host colony or bacteriophage plaque expressing the carboxyterminal portion of the β-gal gene (lacZ). A white or clear colony or plaque indicates the presence of an insert. Because of its water insolubility, X-gal is dissolved in hazardous solvents such as dimethylformamide and then added to the medium following autoclaving. X-gal can be spread on previously plated medium, but this may result in an uneven color development. Also, incubation at 4°C is frequently required for the distinction between a positive recombinant (unstained colony or plaque) and a stained negative. S-Gal™ (3,4-cyclohexenoesculetin β-d-galactopyranoside), a novel β-gal substrate, is autoclavable and microwavable, allowing for dry-blending of the dye directly into the medium. Black S-Gal-stained colonies are visibly distinguishable from unstained colonies at an earlier time than X-gal. In addition, detection of the unstained signal over background is enhanced by 25% using S-Gal-containing medium, compared to medium containing X-gal. These characteristics offer convenience and better suitability for automated colony or plaque analyses. |
| format | Article |
| id | doaj-art-6e2118915d8c4021be22ebc16123017e |
| institution | OA Journals |
| issn | 0736-6205 1940-9818 |
| language | English |
| publishDate | 2001-05-01 |
| publisher | Taylor & Francis Group |
| record_format | Article |
| series | BioTechniques |
| spelling | doaj-art-6e2118915d8c4021be22ebc16123017e2025-08-20T02:25:55ZengTaylor & Francis GroupBioTechniques0736-62051940-98182001-05-013051142114710.2144/01305pf01S-Gal™: An Autoclavable Dye for Color Selection of Cloned DNA InsertsKen Heuermann0Jennifer Cosgrove11Sigma-Aldrich Chemical Company, St. Louis, MO, USA1Sigma-Aldrich Chemical Company, St. Louis, MO, USABlue/white selection is the standard method for detecting a cloned DNA fragment. In the absence of an insert, uninterrupted expression of the vector-encodeda-complement of β-galactosidase (β-gal), results in the hydrolysis of X-gal (5-bromo-4-chloro-3-indolyl β-d-galactoside) and the subsequent blue staining of the host colony or bacteriophage plaque expressing the carboxyterminal portion of the β-gal gene (lacZ). A white or clear colony or plaque indicates the presence of an insert. Because of its water insolubility, X-gal is dissolved in hazardous solvents such as dimethylformamide and then added to the medium following autoclaving. X-gal can be spread on previously plated medium, but this may result in an uneven color development. Also, incubation at 4°C is frequently required for the distinction between a positive recombinant (unstained colony or plaque) and a stained negative. S-Gal™ (3,4-cyclohexenoesculetin β-d-galactopyranoside), a novel β-gal substrate, is autoclavable and microwavable, allowing for dry-blending of the dye directly into the medium. Black S-Gal-stained colonies are visibly distinguishable from unstained colonies at an earlier time than X-gal. In addition, detection of the unstained signal over background is enhanced by 25% using S-Gal-containing medium, compared to medium containing X-gal. These characteristics offer convenience and better suitability for automated colony or plaque analyses.https://www.future-science.com/doi/10.2144/01305pf01 |
| spellingShingle | Ken Heuermann Jennifer Cosgrove S-Gal™: An Autoclavable Dye for Color Selection of Cloned DNA Inserts BioTechniques |
| title | S-Gal™: An Autoclavable Dye for Color Selection of Cloned DNA Inserts |
| title_full | S-Gal™: An Autoclavable Dye for Color Selection of Cloned DNA Inserts |
| title_fullStr | S-Gal™: An Autoclavable Dye for Color Selection of Cloned DNA Inserts |
| title_full_unstemmed | S-Gal™: An Autoclavable Dye for Color Selection of Cloned DNA Inserts |
| title_short | S-Gal™: An Autoclavable Dye for Color Selection of Cloned DNA Inserts |
| title_sort | s gal™ an autoclavable dye for color selection of cloned dna inserts |
| url | https://www.future-science.com/doi/10.2144/01305pf01 |
| work_keys_str_mv | AT kenheuermann sgalanautoclavabledyeforcolorselectionofcloneddnainserts AT jennifercosgrove sgalanautoclavabledyeforcolorselectionofcloneddnainserts |