Instant seasoned mush and its production process

Instant seasoned mush of the present invention consists of seasoned mush powder, which comprises rice flour glutinous rice flour, soybean flour, konjak powder and tea powder and is produced by fryingmaterial powder and mixing; and supplementary material, which includes walnut kernel, peanut and soybean, etc. Before eating, the seasoned mush is mixed with boiled water and the supplementary material is added. It contains rich nutritious components and no food additive and may be eaten in various fields.

Bacillus anthracis detection kit and using method of kit

The invention provides a bacillus anthracis detection kit. The bacillus anthracis detection kit comprises two pairs of primers using bacillus anthracis PA genes as target genes and designed on the basis of a loop-mediated isothermal amplification technology, namely inner primers FIP/BIP and outer primers F3/B3. The bacillus anthracis detection kit has more comprehensive detection effect and low omission rate.

Detection kit for vibrio cholerae O139 group and detection method thereof

The invention relates to a detection kit for a vibrio cholerae O139 group, which comprises BstDNA polymerase, reaction liquid, sample pretreatment liquid, coloration liquid, stabilizing solution and positive control, and also comprises two pairs of primers which take vibrio cholerae wbfR genes as target genes and two pairs of primers which are designed based on the loop-mediated isothermal amplification technology, namely inner primers FIP/BIP and outer primers F3/B3. The detection kit for the vibrio cholerae O139 group has the advantages of comprehensive detection effect, high specificity and low omission factors, and is suitable for the quick detection of the vibrio cholerae O139 group.

Test method and kit for spectinomycin resistant gonococcus

Vibrio cholerae typing and virulence gene detection kit and detection method

The invention relates to a vibrio cholerae typing and virulence gene detection kit and a vibrio cholerae typing and virulence gene detection method. The kit comprises DNA extracting solution, PCR reaction solution, a Taq enzyme system, a positive quality control product and a negative quality control product, wherein the PCR reaction solution consists of PCR reaction buffer, four pairs of forward and reverse primers for the specificity of vibrio cholerae and four probes for the specificity of the vibrio cholerae; the primers and probes are designed according to the specificity conservative areas of nucleic acid sequences of a hemolysin gene, an O-antigen gene of O139 type vibrio cholerae, the O-antigen gene of O1 type vibrio cholerae and the virulence gene of cholera toxin (CTX). The detection kit and the detection method ensure a reliable and stable result, are easy and fast to operate and can realize the typing of the vibrio cholerae and fast judgment about whether the vibrio cholerae ...

Detection kit for vibrio cholerae O139 group and detection method thereof

The invention relates to a detection kit for a vibrio cholerae O139 group, which comprises BstDNA polymerase, reaction liquid, sample pretreatment liquid, coloration liquid, stabilizing solution and positive control, and also comprises two pairs of primers which take vibrio cholerae wbfR genes as target genes and two pairs of primers which are designed based on the loop-mediated isothermal amplification technology, namely inner primers FIP/BIP and outer primers F3/B3. The detection kit for the vibrio cholerae O139 group has the advantages of comprehensive detection effect, high specificity and low omission factors, and is suitable for the quick detection of the vibrio cholerae O139 group.

Fluorescent quantitative PCR detection kit of vibrio parahemolyticus pathogenicity marker gene tdh as well as detection method and application thereof

The invention relates to a kit. The kit comprises a dNTP mixture, PCR reaction liquid, a probe and an amplification primer, wherein the sequence of the probe is shown as SEQ ID NO:1, the forward sequence of the amplification primer is shown as SEQ ID NO:2, and the reverse sequence of the amplification primer is shown as SEQ ID NO:3. The invention also provides a fluorescent quantitative PCR detection method of a vibrio parahemolyticus pathogenicity marker gene tdh. In addition, the invention also provides the application of the kit. The invention has the advantages that a real-time PCR method for quickly detecting a vibrio parahemolyticus tdh gene is constructed, can be used as one of the methods of a vibrio parahemolyticus pathogenicity judgment system and is used for the quarantine quality control of exported and imported marine products. The inventers construct a formula using a vibrio parahemolyticus OD600 value to calculate the absolute quantity and concentration of florae, which can ...

Detection kit for vibrio cholerae O1 group and detection method thereof

The invention relates to a detection kit for a vibrio cholerae O1 group, which comprises BstDNA polymerase, reaction liquid, sample pretreatment liquid, coloration liquid, stabilizing solution and positive control, and also comprises two pairs of primers which take vibrio cholerae RfbN genes as target genes and two pairs of primers which are designed based on the loop-mediated isothermal amplification technology, namely inner primers FIP/BIP and outer primers F3/B3. The detection kit for the vibrio cholerae O1 group has the advantages of comprehensive detection effect, high specificity and low omission factors, and is suitable for the quick detection of the vibrio cholerae O1 group.