Q1:Sometimes color of dehydrated culture media between batches have subtle differences,would this affect test results?
The source and storage conditions of raw material is different ,so there may be a slight difference in color, which is a normal phenomenon. Products from our company have to undergo a rigorous inspection and sensory biology verification before sale, to ensure that all the indicators characteristics of the product is under enterprise standard to the extent permitted, not affect the test results.
Q2: After pouring the liquid medium on the plate , medium seems hard to clot or coagulation time is longer, is it some problem with product quality?
The reason may be: The required hydration in the preparation process have not been done completely .That is to say distilled water is not boil sufficiently to dissolve agar. Because agar proportion, easily settle in the bottom of the bottle, if not fully shaken after
high-temperature sterilization, it will lead to uneven upper agar culture gene content and difficult to set.
Q3: Why some colonies of E. coli chromogenic medium color not shown above, but also confirmed through biochemical tests for E. coli (false negative)?
E. CHROMOGENIC medium is based on the principle of specific enzyme of E. coli and design, 94% of E. coli have β-glucuronidase enzyme, with the chromogenic enzyme substrate medium role in the formation of blue-green colonies. And about 4% of the E. coli does not have β- glucuronidase enzymes, including concern O157: H7 Escherichia coli. Therefore, these E. coli can not be displayed on the color characteristic of E. coli chromogenic medium,it is possible of false-negative on the chromogenic medium. However, the traditional medium of the same can not avoid the problem of false negatives, such as: no gas or slow ferment lactose intolerance may also strain 44.5 false negatives in the conventional medium. For this small part of the E. coli can be detected using other
methods.
Q4:During anaerobic or micro-aerobic culture, is it necessary to remove gas bag from package? How to use oxygen indicator?
During anaerobic or micro-aerobic culture, using method of gassing agent should be done according to the manufacturer's instructions. Remove the paper bag from the plastic packaging, but do not cut the paper bag. Torn the outer packaging of oxygen indicator then it can be used.
5. Who are we?
We are based in Guangdong, China, start from 1993,sell to Domestic Market(80.00%),Southeast Asia(5.00%),Mid East(5.00%),Africa(3.00%),South America(2.00%),North America(1.00%),Eastern Europe(1.00%),South Asia(1.00%),Central America(1.00%),Western Europe(1.00%). There are total about 301-500 people in our office.
6. How can we guarantee quality?
Always a pre-production sample before mass production;
Always final Inspection before shipment;
7.What can you buy from us?
Microbial Detection Product,Peptone&Tryptone,Deydrated Culture Media,Granular Media,Microbial Air Sampler and so on.
8. Why should you buy from us not from other suppliers?
1.With strong R&D capacity and good scientific research conditions,over 30 years of experience 2.Largest culture media manufactuer in China follow international standard 3.Stable high quality main raw material from Europe & strictly quality control
9. What services can we provide?
Accepted Payment Currency:USD,EUR,CNY;
Accepted Payment Type: T/T,MoneyGram,PayPal,Western Union,Cash,Escrow;
Language Spoken:English,Chinese