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100g,1.25L
Use RAPID'E.coli O157:H7 Agar for the detection, isolation, and presumptive identification of E. coli O157:H7 in food products. Results should be confirmed by standard reference methods appropriate for the food type being tested. Confirmation using latex is also validated for colonies isolated from RAPID'E.coli O157:H7 agar.
This product includes 100 g of dehydrated medium. Supplements of novobiocin (10 mg/L) and potassium tellurite (0.8 mg/L) must be added to this medium.
Features and Benefits
- Detection on a single plate
- Typical (sorbitol-/β-glucuronidase-) and atypical (β-glucuronidase+) E. coli O157:H7 colonies are dark blue or black
- Other atypical (sorbitol+) E. coli O157:H7 colonies are blue to turquoise blue
- 100% specificity demonstrated by testing 50 strains of E. coli O157:H7 and 35 other strains
- Selectivity is increased by the addition of novobiocin and other selective agents such as potassium tellurite
- Results with RAPID'E.coli O157:H2 Medium in ≤48 hr
Validations
Certified NF VALIDATION according to the ISO 16140 standard and validated by the AOAC.
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文献和实验Transformation of E. coli by Electroporation
Materials: SOB medium E. coli host strain such as DH5α WB tRNA 5 M ammonium acetate
In recent years several techniques have been described for the introduction of DNA molecules into Escherichia coli . These are based on the findings of Mandel and Higa (1 ), who demonstrated that incubation of cells with naked bacteriophage DNA
1.O/N (5ml E.coli in LB-->1ml into 200ml LB/37℃ 2.Grow 2-3H to A660 ~0.3-0.4 3.Chill cells 10'/ice Spin down 10',5K,4℃ 4.Wash 1X 200ml 10% glycerol (sterile)40℃; Spin down 10',5K,4℃ 5.Wash 1X 40 ml 10% glycerol--> transfer to S34 tubes & spin
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