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平臺(tái)編號(hào)：bio-134319
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國際編號(hào)：ATCC BAA-1088D-5
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拉丁屬名： Genomic DNA from Shewanella loihica strain PV-4
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規(guī)格：Dried
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用途：ATCC原裝進(jìn)口
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服務(wù)費(fèi)用：
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注意事項(xiàng)：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(dòng)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)）
Genomic DNA from Shewanella loihica strain PV-4
Genomic DNA from Shewanella loihica strain PV-4
BAA-1088D-5™
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Genomic DNA isolated from Shewanella loihica strain PV-4. This bacterial strain is also available as ATCC® Catalog No. BAA-1088™.
Product category
Bacteria
Product type
Nucleic acid
Derived from
Shewanella loihica PV-4 (ATCC BAA-1088)
Organism
Shewanella loihica
Type strain
No
Genome sequenced strain
Yes
Applications
Bioinformatics
Next-generation sequencing
Mass
5 μg
Product format
Dried
Shipping information
Stored in 1X TE buffer
Characteristics
Comments
This preparation of high molecular weight DNA is appropriate for use in the polymerase chain reaction (PCR)* process and other molecular biology applications.
*The PCR process is covered by patents owned by Hoffmann-La Roche Inc. Use of the PCR process requires a license. Genomic DNA from Genome sequenced strain
Handling information
Handling procedure
Centrifuge tube prior to opening to prevent loss of pelleted material
Rehydrate contents of vial with molecular grade H2O.
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; then incubate for 1 hour at 65°C. Resuspending the dried DNA in ≥250 µL may give better results.
Handling notes
This preparation of high molecular weight DNA is appropriate for use in the polymerase chain reaction (PCR)* process and other molecular biology applications.
*The PCR process is covered by patents owned by Hoffmann-La Roche Inc. Use of the PCR process requires a license. Genomic DNA from Genome sequenced strain
Quality control specifications
Total amount
Total DNA by PicoGreen® measurement was found to be approximately 5 µg.
Integrity
Integrity 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 tests
Functional activity was confirmed by PCR amplification of the 16S ribosomal RNA gene.
Identity
Identity confirmed by sequencing of 16S ribosomal RNA gene (first ~500 base pairs).
Verification method
Whole-genome Sequencing
