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Qiaamp dsp blood mini kit

Manufactured by Qiagen

The QiaAmp DSP Blood Mini Kit is a laboratory equipment product designed for the purification of DNA from small volumes of whole blood samples. It utilizes a silica-based membrane technology to efficiently extract and concentrate DNA, which can then be used for various downstream applications.

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2 protocols using qiaamp dsp blood mini kit

1

FcγRIIb Genotyping from Cord Blood

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Genotyping of cord blood samples for FcγRIIb alleles was done as described before (Baerenwaldt et al., 2011 (link)). In brief, genomic DNA was isolated with the „QiaAmp DSP Blood Mini Kit “(Qiagen, Hilden) following the instructions of distributor. FcγRIIB genotyping was carried out with a two-step PCR protocol. Briefly, a 15 kb product was amplified using the Qiagen ‘LongRange PCR Kit’ (Qiagen) (Primers LongRange fwd: ctccacaggttactcgtttctaccttatcttac and LongRange rev: gcttgcgtggcccctggttctca) generating a 14.7 kb amplicon which was purified via gel electrophoresis and by using the Qiagen ‘Gel purification Kit’. This PCR product was used as a template for the nested PCR to amplify the transmembrane region (Primers R2Btm-fwd: aaggggagcccttccctctgtt and R2Btm-rev: gtggcccctggttctcagaa). Subsequently, the PCR product (2365 bp) was gel purified and sequenced (using the R2Bseq primer: aaggggagcccttccctctgtt).
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2

Genotyping of FcγRIIb alleles

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Genotyping of blood samples for FcγRIIb alleles was done as described before [14 (link)]. Briefly, genomic DNA was isolated with the „QiaAmp DSP Blood Mini Kit “(Qiagen, Hilden) according to the manufactureŕs instructions. For FcγRIIb genotyping a two-step PCR protocol was followed: Firstly, a 15 kb product was amplified using the Qiagen ‘LongRange PCR Kit’ (Qiagen) (Primers LongRange fwd: ctccacaggttactcgtttctaccttatcttac and LongRange rev: gcttgcgtggcccctggttctca) generating a 14.7 kb amplicon. Following purification by gel electrophoresis with the Qiagen ‘Gel purification Kit’, the PCR product was used as a template for the nested PCR (Primers R2Btm-fwd: aaggggagcccttccctctgtt and R2Btm-rev: gtggcccctggttctcagaa). Finally, the PCR product (2365 bp) containing the transmembrane region was purified and sequenced (using the R2Bseq primer: aaggggagcccttccctctgtt).
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