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Suremda

Manufactured by Illumina
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Sourced in United States

SureMDA is a lab equipment product manufactured by Illumina. It performs Multiple Displacement Amplification (MDA) to generate high-quality, high-molecular-weight DNA from small samples. SureMDA is designed to amplify DNA from a variety of sample types, including single cells, FFPE samples, and low-input genomic DNA.

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Lab products found in correlation

Sureplex, by Illumina (2 mentions)

Spelling variants of this product

REPLI-g Single Cell Kit multiple displacement amplification (SureMDA (2 citations)

2 protocols using suremda

1

Polar Body Aneuploidy Screening

Check if the same lab product or an alternative is used in the 5 most similar protocols
In another PGS case, in which array CGH had been used to detect aneuploidy by copy number analysis of both polar bodies, the WGA products (Sureplex; Illumina, San Diego, CA, USA) from both polar bodies were SNP genotyped along with parental genomic DNAs and, with patients informed consent, WGA products (SureMDA; Illumina, San Diego, CA, USA) of nine corresponding fertilised embryos which had all been diagnosed as aneuploid.
Ottolini C.S., Newnham L., Capalbo A., Natesan S.A., Joshi H.A., Cimadomo D., Griffin D.K., Sage K., Summers M.C., Thornhill A.R., Housworth E., Herbert A.D., Rienzi L., Ubaldi F.M., Handyside A.H, & Hoffmann E.R. (2015). “Genome-wide recombination and chromosome segregation in human oocytes and embryos reveal selection for maternal recombination rates”. Nature genetics, 47(7), 727-735.
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2

Polar Body Aneuploidy Screening

Check if the same lab product or an alternative is used in the 5 most similar protocols
In another PGS case, in which array CGH had been used to detect aneuploidy by copy number analysis of both polar bodies, the WGA products (Sureplex; Illumina, San Diego, CA, USA) from both polar bodies were SNP genotyped along with parental genomic DNAs and, with patients informed consent, WGA products (SureMDA; Illumina, San Diego, CA, USA) of nine corresponding fertilised embryos which had all been diagnosed as aneuploid.
Ottolini C.S., Newnham L., Capalbo A., Natesan S.A., Joshi H.A., Cimadomo D., Griffin D.K., Sage K., Summers M.C., Thornhill A.R., Housworth E., Herbert A.D., Rienzi L., Ubaldi F.M., Handyside A.H, & Hoffmann E.R. (2015). “Genome-wide recombination and chromosome segregation in human oocytes and embryos reveal selection for maternal recombination rates”. Nature genetics, 47(7), 727-735.
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