Vibrio cholerae Z132, DNA (10 µg)

PRODUCT DESCRIPTION: Each aliquot contains 10 µg of DNA extracted from a pure culture of Vibrio cholerae. The identification of this organism was confirmed by 16S sequencing. The purity of the culture was monitored by Gram staining and by additional culturing. The DNA was extracted from the cells following the bacterial protocol from the Qiagen®Genomic DNA Handbook using Qiagen®Genomic DNA Buffers with a 500/G genomic tip.DNA concentration and A260/280 ratios are determined using a NanoDrop ND-1000®. The extracted DNA also tested positive on an inhouse real time PCR assay.

INTENDED USE: Purified Genomic DNA is designed for use as an amplification and/or detection control for nucleic acid testing of Vibrio cholerae. It can also be used to determine a limit of detection (LOD), in diagnostic assay development, cross-reactivity studies or genomic sequencing. When used as a control for nucleic acid tests, the same protocols as those used to amplify extracted clinical specimens should be employed.

PRECAUTIONS:
- Use Universal Precautions when handling Genomic DNA.
- The material may be re-frozen after thawing. Repetitive freezing and thawing is not recommended (aliquot material if necessary).
- To avoid cross-contamination, use separate pipette tips for all reagents.

RECOMMENDED STORAGE: This control is supplied in TE Buffer and should be frozen at -20°C or below.

DO NOT USE IN HUMANS: These products are intended for research, product development or manufacturing use only. These products are NOT intended for use in the manufacture or processing of injectable products subject to licensure under section 351 of the Public Health Service Act or for any other product intended for administration to humans.

Escherichia coli O111:NM, DNA (10 µg)

PRODUCT DESCRIPTION: Each aliquot contains 10 µg of DNA extracted from a pure culture of Escherichia coli. The identification of this organism was confirmed by 16S sequencing. The purity of the culture was monitored by Gram staining and by additional culturing. he DNA was extracted from the cells following the bacterial protocol from the Qiagen®Genomic DNA Handbook using Qiagen®Genomic DNA Buffers with a 500/G genomic tip.DNA concentration and A260/280 ratios are determined using a NanoDrop ND-1000®. The extracted DNA also tested positive on an inhouse real time PCR assay.

INTENDED USE: Purified Genomic DNA is designed for use as an amplification and/or detection control for nucleic acid testing of Escherichia coli. It can also be used to determine a limit of detection (LOD), in diagnostic assay development, cross-reactivity studies or enomic sequencing. When used as a control for nucleic acid tests, the same protocols as those used to amplify extracted clinical specimens should be employed.

PRECAUTIONS:
- Use Universal Precautions when handling Genomic DNA.
- The material may be re-frozen after thawing. Repetitive freezing and thawing is not recommended (aliquot material if necessary).
- To avoid cross-contamination, use separate pipette tips for all reagents.

RECOMMENDED STORAGE: This control is supplied in TE Buffer and should be frozen at -20°C or below.

Plesiomonas shigelloides Z130, DNA (10 µg)

PRODUCT DESCRIPTION: Each aliquot contains 10 µg of DNA extracted from a pure culture of Plesiomonas shigelloides. The identification of this organism was confirmed by 16S sequencing. The purity of the culture was monitored by Gram staining and by dditional culturing. The DNA was extracted from the cells following the bacterial protocol from the Qiagen® Genomic DNA Handbook using Qiagen® Genomic DNA Buffers with a 500/G genomic tip. DNA concentration and A260/280 ratios are determined using a NanoDrop ND-1000®. The extracted DNA also tested positive on an inhouse real time PCR assay.

INTENDED USE: Purified Genomic DNA is designed for use as an amplification and/or detection control for nucleic acid testing of Plesiomonas shigelloides. It can also be used to determine a limit of detection (LOD), in diagnostic assay development, crossreactivity tudies or genomic sequencing. When used as a control for nucleic acid tests, the same protocols as those used to amplify extracted clinical specimens should be employed.

PRECAUTIONS:
- Use Universal Precautions when handling Genomic DNA.
- The material may be re-frozen after thawing. Repetitive freezing and thawing is not recommended (aliquot material if necessary).
- To avoid cross-contamination, use separate pipette tips for all reagents.

RECOMMENDED STORAGE: This control is supplied in TE Buffer and should be frozen at -20°C or below.