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Boehringer Mannheim high prime dna labeling kit
High Prime Dna Labeling Kit, supplied by Boehringer Mannheim, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/high+prime+labelling+kit/high+prime+dna+labeling+kit/us11566256-1940-23-28
Average 90 stars, based on 1 article reviews
high prime dna labeling kit - by Bioz Stars, 2026-10
90/100 stars

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Related Articles

other:

Article Title: Isolation and characterization of α-tubulin genes fromSeptoria tritici andRhynchosporium secalis, and comparative analysis of fungal α-tubulin sequences
Article Snippet: The a-tubulin genes from Septoria tritici and Rhynchosporium secalis have been cloned and sequenced.. The predicted amino acid sequence and intron structure showed strong homology with other known filamentous fungal a-tubulins.. Comparison of sixteen fungal a-tubulin sequences based on amino acid sequence homology and intron structure identified five groups of proteins.

cDNA Library Assay:

Article Title: Recombinant platelet collagen receptor glycoprotein vi and its pharmaceutical use
Article Snippet: The PCR conditions were 5 cycles at 37° C. followed by 30 cycles at 44° C. The sense 19mer 5′ TYATHCCNGCNATGAARMG 3′ (SEQ ID NO: 4) and the antisense 20mer 5′ TTRTANARNGCRAAYTGRTC 3′ (SEQ ID NO: 6) amplified a 221 bp fragment which was subcloned in Bluescript KS+ (Stratagene, La Jolla, Calif.) and sequenced using the T7 Sequenase kit (Amersham, Switzerland). .. Screening the λgt11 cDNA Library with the 221 bp GPVI Probe The 221 bp fragment was cut from the plasmid, cleaned and labelled with α32P-ATP (20 MBq/50 μl, Hartmann Analytik, Braunschweig, Germany) using the High Prime Labelling kit (Boehringer Mannheim, Switzerland). ..

Plasmid Preparation:

Article Title: Recombinant platelet collagen receptor glycoprotein vi and its pharmaceutical use
Article Snippet: The PCR conditions were 5 cycles at 37° C. followed by 30 cycles at 44° C. The sense 19mer 5′ TYATHCCNGCNATGAARMG 3′ (SEQ ID NO: 4) and the antisense 20mer 5′ TTRTANARNGCRAAYTGRTC 3′ (SEQ ID NO: 6) amplified a 221 bp fragment which was subcloned in Bluescript KS+ (Stratagene, La Jolla, Calif.) and sequenced using the T7 Sequenase kit (Amersham, Switzerland). .. Screening the λgt11 cDNA Library with the 221 bp GPVI Probe The 221 bp fragment was cut from the plasmid, cleaned and labelled with α32P-ATP (20 MBq/50 μl, Hartmann Analytik, Braunschweig, Germany) using the High Prime Labelling kit (Boehringer Mannheim, Switzerland). ..



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