RNA Storage Buffer
MCLAB's RNA Storage Buffer, with optimized reagents and pH value, provides better preservation and greater RNA stability for valuable RNA samples than the standard EDTA and TE Buffer or just water.
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The β-galactosidase substrate X-Gal (5-bromo-4-chloro-3-indolyl-β-D-galactopyranoside) is a chromogenic stain for β-gal activity, and is commonly used to distinguish between recombinants and nonrecombinants by lacZ α-complementation with appropriate vectors and hosts.
Description
The β-galactosidase substrate X-Gal (5-bromo-4-chloro-3-indolyl-β-D-galactopyranoside) is a chromogenic stain for β-gal activity, and is commonly used to distinguish between recombinants and nonrecombinants by lacZ α-complementation with appropriate vectors and hosts. X-Gal Solution is provided as a convenient soution with 20 mg/ml concentrate in DMSO, ready for dilution to culture medium or appropriate buffers.
Synonym: 5-Bromo-4-chloro-3-indolyl β-D-galactoside, BCIG, X-Gal
Applications:
Blue/white colony screening assay (blue: non-recombinant colonies & white: recombinant colonies).
X-Gal staining of eukaryotic cells for the detection of β-galactosidase reporter gene expression.
Detection of β-galactosidase activity in various immunological and histochemical applications.
Formula: C14H15BrClNO6
Note
- Petri dish (9 cm diameter): Spread 40 µL on the surface
- Liquid LB agar: Use 2 µL for each 1 mL of liquid LB agar, add just before pouring plates (at about 50°C)
- Transfected eukaryotic cells: use 25 µL (1 mg) for each 1 mL of staining solution
Recommended Storage Condition: Stable up to 6 months when stored and protected from light at 4°C.
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MCLAB's RNA Storage Buffer, with optimized reagents and pH value, provides better preservation and greater RNA stability for valuable RNA samples than the standard EDTA and TE Buffer or just water.
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The β-galactosidase substrate X-Gal (5-bromo-4-chloro-3-indolyl-β-D-galactopyranoside) is a chromogenic stain for β-gal activity, and is commonly used to distinguish between recombinants and nonrecombinants by lacZ α-complementation with appropriate vectors and hosts.
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