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 VC 1kb DNA Ladder NL1409 NL1410 NL1411 NL1412|产品详情|进口橙子视频旧款采购网




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    订购信息
    上海橙子视频app安卓下载生物科技公司
    Tel:400-968-7988    021-33779008
    VC 1kb DNA Ladder
    品牌:Vivantis Technologies
    货号:NL1409 NL1410 NL1411 NL1412
    规格:50 μg 5 x 50 μg 50 μg 5 x 50 μg
    货期:

    Home Ladders/ Markers/Nucleic Acids/ Nucleotides DNA Ladders & Marker VC 1kb DNA Ladder VC 1kb DNA Ladder Description Serves as molecular weight standards for agarose gel electrophoresis. Suitable for sizing of PCR products or other double-stranded DNA fragments. Fragments with size 2500bp are higher in intensity in comparison to other bands to serve as orientation points.

    商品详情 参考文献 相关资料
    Home  Ladders/ Markers/Nucleic Acids/ Nucleotides  DNA Ladders & Marker  VC 1kb DNA Ladder

    VC 1kb DNA Ladder

    Description
    Serves as molecular weight standards for agarose gel electrophoresis. Suitable for sizing of PCR products or other double-stranded DNA fragments. Fragments with size 2500bp are higher in intensity in comparison to other bands to serve as orientation points.

    Storage Buffer
    10mM Tris-HCl (pH 8.0) and 1mM EDTA. Store at -20°C

    6X Loading Dye Solution
    10mM Tris-HCl (pH 8.0), 60mM EDTA, 0.03% bromophenol blue, 0.03% xylene cyanol FF and 60% glycerol

    Usage Recommendation 
    Use 0.05-0.10μg of the DNA ladder per 1mm width of gel lane

    Ordering Information

    Catalog No Description Pack Size
    NL1409 VC 1kb DNA Ladder 50 μg
    NL1410 VC 1kb DNA Ladder 5 x 50 μg
    NL1411 VC 1kb DNA Ladder (ready-to-use) 50 μg
    NL1412 VC 1kb DNA Ladder (ready-to-use) 5 x 50 μg

    Download
    Manual

    VC 1kb DNA Ladder (ready-to-use)

    Publication
    This Product Has Been Used In:
    Chong,S.Y., Rao, P.V., Soon, J.M. (2017). Identification of Escherichia spp. strains in street-vended beverages and associated preparation surfaces using 16S rRNA analysis, International Food Research Journal, Vol. 4, No. 4, 1811-1818
    Siti-Hasmah, M., Hwe-San, L., Xiao-Ying, C., Massawe, F., Abdul-Rahman, O. (2017). Single Nucleotide Modification of VP2 Gene of Highly Virulent Infectious Bursal Disease Virus for Effective Expression Strategy in Tobacco. . Open Access Journal of Microbiology & Biotechnology, Vol. 2, No. 1 (2017). 
    Kepel, B., & Fatimawali, D. (2015) Analysis of 16SrNA Gene and Mercury Reduction Ability of Mercury Resistant Bacteria Isolated from Feces of Patient with Mercury Amalgam at Puskesmas Bahu in Manado. Jurnal Kedokteran Yarsi23(1), p.45-55.
    Khodabandehloo, M., Hosseini, W., Rahmani, M., Rezaee, M., Hakhamaneshi, M., Nikkhoo, B., Jalili, A. (2013). No Detection of Xenotropic Murine Leukemia Virus-Related Viruses in Prostate Cancer in Sanandaj, West of Iran, Asian Pacific Journal of Cancer Prevention, Vol. 14, No. 11, 6929-6933 (2013).
    Khodadad, M., Hosseini, S.Y., Shenavar,F., Erfani, N., Bina, S., Ahmadian, S., Fattahi, M, Hajhosseini,R. (2015). Construction of expressing vectors including melanoma differentiation‐associated gene‐7 (mda‐7) fused with the RGD sequences for better tumor targeting, Iranian Journal of Basic Medical Sciences, Vol. 18, No. 8, 780-787 (2015).
    Ng, K.C.S., & Rivera, W.L. (2015)Multiplex PCR-based Serogrouping and Serotyping of Salmonella enterica from Tonsil and Jejunum with Jejunal Lymph Nodes of Slaughtered Swine in Metro Manila, Philippines Journal of Food ProtectionProQuest. 78(5), p. 873-880
    Sahilah, A.M. et al (2014) Antiobiotic Resistance and Molecular Typing among Cockle (Anadara granosa) Strains of Vibrio parahaemolyticus by Polymerase Chain Reaction (PCR)-based Analysis. World Journal of Microbiology and Biotechnology.ProQuest. 30, p. 649-659. 
    Adzitey et al. (2013)Genotyping of Salmonella Strains Isolated from Ducks, Their Rearing and Processing Environments in Penang, Malaysia, Using RAPD 3 Biotec3(6): 521–527 
    Khodadad, M., et al. (2013) Constuction of Expressing Vectors Including Melanoma Differentiation-Associated Gene-7 (mda-7) Fused With the RGD Sequences for Better Tumor Targeting. Iranian Journal of Basic Medical Sciences. 18(8), p. 780-787.

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