Salmonella pullorum and gallinarum positive serum (DAGF-121)

Salmonella pullorum and gallinarum positive serum

Nature
Native
Tag/Conjugate
Unconjugated
Alternative Names
S. pullorum; S. gallinarum; salmonella pullorum; salmonella gallinarum; serum
Procedure
None
Format
Liquid
Concentration
Batch dependent - please inquire should you have specific requirements.
Size
1ml
Preservative
None
Storage
Store at -20°C or lower. Avoid repeated freeze/thaw cycles
Antigen Description
In blood, the serum is the component that is neither a blood cell (serum does not contain white or red blood cells) nor a clotting factor; it is the blood plasma not including the fibrinogens. Serum includes all proteins not used in blood clotting (coagulation) and all the electrolytes, antibodies, antigens, hormones, and any exogenous substances (e.g., drugs and microorganisms). A study of serum is serology, and may also include proteomics. Serum is used in numerous diagnostic tests, as well as blood typing.
Keywords
S. pullorum; S. gallinarum; salmonella pullorum; salmonella gallinarum; serum

Citations


Have you cited DAGF-121 in a publication? Let us know and earn a reward for your research.

Customer Reviews


Write a review, share your experiences with others and get rewarded !
Product Name Cat. No. Applications Host Species Datasheet Price Add to Basket
Product Name Cat. No. Applications Host Species Datasheet Price Add to Basket

References


Impact of liquid hog manure applications on antibiotic resistance genes concentration in soil and drainage water in field crops

CANADIAN JOURNAL OF MICROBIOLOGY

Authors: Larouche, Elodie; Genereux, Mylene; Tremblay, Marie-Eve; Rhouma, Mohamed; Gasser, Marc-Olivier; Quessy, Sylvain; Cote, Caroline

Agricultural practices such as manure applications could contribute to the spread of antibiotic resistance genes (ARGs) within the environment. Our objective was to assess the impact of certain fertilization methods (mineral or manure) and tillage practices (reduced or conventional) on the presence of ARGs and bacteria in soil and drainage water under wheat and grain corn crops. Targeted ARGs tet(T), sul1, and bla(CTX-M-1) in liquid hog manure, soil, and water samples were quantified by qPCR. Conventional PCR was used to detect mcr-1 and mcr-2. ARGs in control plots were detected despite the absence of manure, representing an environmental reservoir of resistant microorganisms. The manure application rate higher than 39 m(3)/ha increased tet(T) and sul1 gene concentrations in soil for more than 180 days. Tillage practices had no impact on ARG concentrations in soil and water samples. The bla(CTX-M-1) gene was only detected in seven water samples in 2016, but no link was established with the treatments. The mcr-1 and mcr-2 genes were not detected in all tested samples. This study demonstrated that tet(T) and sul1 gene concentrations increased in soil after liquid hog manure application as well as in drainage water in the next weeks.

Biodegradation of Novacron Turqueiose (Reactive Blue 21) by Pseudomonas aeruginosa

JOURNAL OF THE CHEMICAL SOCIETY OF PAKISTAN

Authors: Ikram, Muhammad; Zahoor, Muhammad; Khan, Ezzat; Khayam, Sahibzada Muhammad Umar

In the present study four bacterial strains Escherichia Coli, Salmonella typhi, Shiegella and Pseudomonas aeruginosa were used to evaluate their dye decolorization/degradation ability. Out of these bacterial strains Pseudomonas aeruginosa exhibited high potential for selected dye decolorization and hence it was used in subsequent experiments. The effect of dye concentration, pH, temperature, time, glucose and sodium chloride concentrations on decolorization were also studied to determine the optimal conditions required for maximum decolorization/degradation of selected dye by Pseudomonas aeruginosa. Maximum decolorization was observed at: 0.01 mg/L dye concentration, pH 10, temperature 45 degrees C, 0.1 mg/L glucose concentration, 0.1 mg/L sodium chloride concentration and 3 days incubation period at 37 degrees C. The metabolites formed after degradation by selected bacteria at optimum conditions were isolated and characterized by FTIR and mass spectrometry. In the mass spectra molecular ion peak was not observed and it was difficult to draw a conclusion from it. However, FTIR spectra provided some valuable information. The peaks at 1301.8 cm(-1) for C-N and 1231.5 cm(-1) for O-H stretch observed for original dye were completely absent in the decolorized products. The disappearance of C-N (part of the porphyrin ring system) peak in FTIR spectra shows that the porphyrin ring has been destroyed by bacteria. The extensive fragmentations in the mass spectra also confirm the degradation of the dye parental structure.

Online Inquiry

Name:
Phone: *
E-mail Address: *
Technology Interest:
Type of Organization:
Service & Products Interested: *
Project Description:
Verification code
Click image to refresh the verification code.

Online Inquiry

  Interested in larger quantities ? request a quote!
  Protocol may be improved. Please feel free to contact us to obtain the latest version.!

Ordering Information

Payment methods we support:
Invoice / Purchase Order
Credit card

OUR PROMISE TO YOU Guaranteed product quality expert customer support

Inquiry Basket