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首頁>美國ATCC>ATCC菌種類>Genomic DNA from Aspergillus niger strain 4247
Genomic DNA from Aspergillus niger strain 4247
    Genomic DNA from Aspergillus niger strain 4247
  • 平臺編號:bio-74125
  • 國際編號:ATCC 6275D-2
  • 拉丁屬名: Aspergillus niger
  • 規(guī)格:freeze-dried
  • 用途:ATCC原裝進(jìn)口
  • 服務(wù)費用:
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  • 訂購 說明書
  • 注意事項:僅用于科學(xué)研究或者工業(yè)應(yīng)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(zhǔn))

Product categoryFungi

Product typeNucleic acid

Derived fromAspergillus niger 4247 [AM 324, CBS 131.52, CBS 769.97, DSM 1957, IFO 6341, IMI 45551, J. Friedrich A98, KCC F-0086, NRRL 334, QM 324, QM 458, Steinberg, TC 215-4247, WB 334] (ATCC 6275)

OrganismAspergillus niger van Tieghem

Type strainNoGenome sequenced strainYesApplicationsNext-generation sequencing

Mass2 μgProduct formatFreeze-dried 

Characteristics

CommentsThis preparation of high molecular weight DNA is appropriate for use in the polymerase chain reaction (PCR) process and other molecular biology applications.

Handling information

Handling procedureCentrifuge tube prior to opening to prevent loss of pelleted material

DNA is dried in 1X TE buffer. Rehydrate contents of vial with a desired amount of molecular grade water or any preferred buffer. Resuspending the dried DNA in ≥250 μL may give better results.

Place vial at 37°C for 1 hour, or at 2°C to 8°C overnight.

For more complete rehydration and to fully recover DNA, incubate the sample overnight at 4°C while rocking.

To enhance PCR efficiency, add 1 μL of freshly prepared dry milk powder solution (50 mg/mL) to a PCR mix (25 to 50 μL). PCR with “hot start” is also recommended for better results.

Handling notesGenomic DNA is appropriate for PCR and other molecular biology applications.

Quality control specifications

Electrophoresis - RNA contentNo RNA was detected by electrophoresisPurity (A260/A280)1.7 to 2.1IntegrityIntegrity of DNA was determined by electrophoresis on a 1% agarose gel stained with SYBR Safe™, and was found to be of high molecular weight.Functional testsFunctional activity was confirmed by PCR amplification of approximately 1500 base pairs fragment of rRNA gene cluster including ITS1-5.8S-ITS2 region.IdentityIdentity confirmed by sequencing of ITS1, 5.8S gene and ITS2 regions of ribosomal RNA (~ 500 base pairs).Verification methodWhole-genome Sequencing

 

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