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Chromatein Prestained Protein Ladder (ready-to-use) PR0602|产品详情|进口橙子视频旧款采购网




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    Chromatein Prestained Protein Ladder (ready-to-use)
    品牌:Vivantis Technologies
    货号:PR0602
    规格:2 x 250 μl
    货期:

    Home Ladders/ Markers/Nucleic Acids/ Nucleotides Protein Ladders & Markers Chromatein Prestained Protein Ladder Chromatein Prestained Protein Ladder Description Chromatein Prestained Protein Ladder contains 11 proteins that resolve into sharp, tight bands in the range of 10-175 kDa. It is supplied in a loading buffer for direct loading on gels. Allows monitoring molecular weight separation d

    商品详情 参考文献 相关资料
    Home  Ladders/ Markers/Nucleic Acids/ Nucleotides  Protein Ladders & Markers  Chromatein Prestained Protein Ladder

    Chromatein Prestained Protein Ladder

    Description
    Chromatein Prestained Protein Ladder contains 11 proteins that resolve into sharp, tight bands in the range of 10-175 kDa. It is supplied in a loading buffer for direct loading on gels. Allows monitoring molecular weight separation during electrophoresis, estimation of molecular weights of interest and evalsuate western transfer efficiency.

    Feature
    Broad Range: 10-175kDa 
    Convenient: Supplied in a loading buffer for direct loading
    Easy Identification: ~10, ~40, and ~90kDa reference bands coupled with a blue dye

    Quality Control
    Tested in SDS-polyacrylamide gel electrophoresis and western blotting

    Storage

    • Stable at 4°C for 3 months
    • Store at -20°C for 24 months

     

    Ordering Information

    Catalog No Description Pack Size
    PR0602 Chromatein Prestained Protein Ladder (ready-to-use) 2 x 250 μl

    Download
    Manual

    Chromatein Prestained Protein Ladder

    Publication
    This Product Has Been Used In: 
    Dehnaiv, E., Fathi-Roudsari,M., Mirzaie, S., Arab., S.S., Siadat, S.O.R., Khajeh, K. (2017) Engineering disulfide bonds in Selenomonas ruminantium B-xylosidase by experimental and computational methods. International Journal of Biological Macromolecules. 95. Pp.248-255 
    Karimi, M., Biria, D. (2016) ) The synergetic effect of starch and alpha amylase on the biodegradation of n-alkanes 
    Golshani, M., et al. (2016) In silico Analysis of Brucella abortus 0mp2b and In vitro Expression of S0mp2b. Clinical and Experimental Vaccine Research. 5(1), p.75-82. 
    Golshani, M., Rafati, S., Siadat, S.D.,Nejati-Moheimani, M., Shahcheraghi, F., Arsang, A., Bouzari, S. (2015) Improved immunogenicity and protective efficacy of a divalent DNA vaccine encoding Brucella L7/L12-truncated Omp31 fusion protein by a DNA priming and protein boosting regimen. Molecular Immunology 66. Pp.384-391. 
    Ungcharoenwiwat, P., H-Kittikun A. (2015) Purification and characterization of lipase from Burkholderia sp. EQ3 isolated from wastewater from a canned fish factory and its application for the synthesis of wax esters. Journal of Molecular Catalysis B: Enzymatic.115. Pp..96-104 
    Thongsaiklaing, T., et al. (2014)Analysis of the α-amylase Gene Sequence and the Enzyme Activity of Indian Rock Oyster Saccostrea forskali . Fisheries ScienceProQuest. p. 589-601. 
    Gharajelar, S.N., Ahmadi, M., & Hosseini, B. (2012) 2015) Cloning and Expression of the Immunogenic Moiety of Pseudomonas aeruginosa Exotoxin A Biological Journal of Microorganism1(4), p. 7-14.

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