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首頁>美國ATCC>ATCC菌種類>Quantitative Genomic DNA from Plesiomonas shigelloides strain CDC 3085-55
Quantitative Genomic DNA from Plesiomonas shigelloides strain CDC 3085-55
    Quantitative Genomic DNA from Plesiomonas shigelloides strain CDC 3085-55
  • 平臺編號:bio-56664
  • 國際編號:ATCC 14029DQ
  • 拉丁屬名: Plesiomonas shigelloides
  • 規(guī)格:Frozen
  • 用途:ATCC原裝進口
  • 服務費用:
    加載中……
  • 訂購 說明書
  • 注意事項:僅用于科學研究或者工業(yè)應用等非醫(yī)療目的不可用于人類或動物的臨床診斷或治療,非藥用,非食用(產(chǎn)品信息以出庫為準)

 Quantitative Genomic DNA from Plesiomonas shigelloides strain CDC 3085-55

14029DQ ™

Quantitative genomic DNA from Plesiomonas shigelloides strain CDC 3085-55 can be used for assay development, verification, and validation as well as monitoring of day-to-day test variation and lot-to-lot performance of molecular-based assays. The quantitative format allows for the generation of a standard curve for quantitative PCR (qPCR) to determine bacterial load.

Product category

Bacteria

Product type

Molecular standard

Nucleic acid

Derived from

Plesiomonas shigelloides CDC 3085-55 [Bader M51, NCIB 9242, NCTC 10360, RH 798] (ATCC 14029)

Organism

Plesiomonas shigelloides (Bader) Habs and Schubert

Type strain

Yes

Genome sequenced strain

Yes

Applications

Assay development

Enteric disease research

Infectious disease research

Specification range ≥1 x 105 copies/μL

Volume 100 μL

Product format

Frozen

Storage conditions -20°C or colder

General

Specific applications

ATCC Genuine Nucleics can be used for assay development, verification, and validation as well as monitoring of day-to-day test variation and lot-to-lot performance of molecular-based assays. The quantitative format allows for the generation of a standard curve for quantitative PCR (qPCR) to determine bacterial load.

Characteristics

Comments

Genomic DNA isolated from a preparation of Plesiomonas shigelloides strain CDC 3085-55 (ATCC 14029). The source organism is also available through the ATCC catalog.

Handling information

Handling procedure

Thaw the vial at room temperature and immediately place on ice. Avoid exposing the DNA to repeated freeze-thaw cycles as it may result in degradation.

Gently mix the sample to ensure an even distribution of material.

Briefly centrifuge the tube before opening to ensure all liquid is at the bottom.

Handling notes

Aliquoting is highly recommended to avoid multiple freeze-thaws.

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