lightcycler probe design2 software (Roche)
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lightcycler probe design2 software
Lightcycler Probe Design2 Software, supplied by Roche, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/lightcycler+probe+design2+software/pm23783460-47-14-18
Average 86 stars, based on 1 article reviews
Lightcycler Probe Design2 Software, supplied by Roche, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/lightcycler+probe+design2+software/pm23783460-47-14-18
Average 86 stars, based on 1 article reviews
lightcycler probe design2 software - by Bioz Stars,
2026-09
86/100 stars
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Polymerase Chain Reaction:Article Title: The mitochondrial solute carrier SLC25A5 at Xq24 is a novel candidate gene for non-syndromic intellectual disability. Article Snippet: Loss-of-function mutations in several different neuronal pathways have been related to intellectual disability (ID).. Such mutations often are found on the X chromosome in males since they result in functional null alleles.. So far, microdeletions at Xq24 reported in males always have been associated with a syndromic form of ID due to the loss of UBE2A. Real-time Polymerase Chain Reaction:Article Title: The mitochondrial solute carrier SLC25A5 at Xq24 is a novel candidate gene for non-syndromic intellectual disability. Article Snippet: Loss-of-function mutations in several different neuronal pathways have been related to intellectual disability (ID).. Such mutations often are found on the X chromosome in males since they result in functional null alleles.. So far, microdeletions at Xq24 reported in males always have been associated with a syndromic form of ID due to the loss of UBE2A. Generated:Article Title: The mitochondrial solute carrier SLC25A5 at Xq24 is a novel candidate gene for non-syndromic intellectual disability. Article Snippet: Loss-of-function mutations in several different neuronal pathways have been related to intellectual disability (ID).. Such mutations often are found on the X chromosome in males since they result in functional null alleles.. So far, microdeletions at Xq24 reported in males always have been associated with a syndromic form of ID due to the loss of UBE2A. Software:Article Title: The mitochondrial solute carrier SLC25A5 at Xq24 is a novel candidate gene for non-syndromic intellectual disability. Article Snippet: Loss-of-function mutations in several different neuronal pathways have been related to intellectual disability (ID).. Such mutations often are found on the X chromosome in males since they result in functional null alleles.. So far, microdeletions at Xq24 reported in males always have been associated with a syndromic form of ID due to the loss of UBE2A. Article Title: Application of three duplex real-time PCR assays for simultaneous detection of human seasonal and avian influenza viruses. Article Snippet: The most specific and conserved target regions were identified following multiple alignments of the nucleotide sequences of the respective HA/NA/NS genes of different influenza virus strains available from the Influenza Sequence Database (ISD) [19] and GenBank database (National Center of Biotechnology Information). .. Primer and probe sets were T a b le 1 S eq u en ce s o f p ri m er s an d p ro b es d es ig n ed an d se le ct ed fo r u se in th e q P C R as sa y s N am e O li g o n u cl eo ti d e se q u en ce (5 ’– 3 ’) F lu o ro p h o re (5 ’/ 3 ’) A m p li co n le n g th (n t) T ar g et (g en e) N u cl eo ti d e p o si ti o n s G en B an k ac ce ss io n n o . o f re fe re n ce se q u en ce H 1 v _ F G T A T T A T C A T T T C A G A T A C A C C A G T C C 8 4 2 -8 6 8 H 1 v _ R G A C A T T T T C C A A T T G T G A T C G G 1 1 9 H A 9 6 1 -9 4 0 F J9 8 1 6 1 3 H 1 v _ P A A C A C C A G C C T C C C A T T T C A G A A JO E /B H Q 1 9 1 0 -9 3 2 (H 1 N 1 )p d m 0 9 H 3 _ F T T G A T T A A C A G C A C A G G G A A T C T A 7 7 8 -8 0 1 H 3 _ R T G C A T T C A G A A T T G C A T T T G C C 1 1 4 H A 8 9 2 -8 2 1 G Q 2 9 3 0 8 1 H 3 _ P A G C T C A A T A A T G A G A T C A G A T G C A C C C F R 6 1 0 /B H Q 2 8 4 1 -8 6 6 H 3 N 2 H 5 _ F T T T C A T T G C T C C A G A A T A T G C A T A C A 7 8 6 -8 1 1 H 5 _ R G G A A T G G C A T A C T A G A G T T T A T C G 1 3 6 H A 9 2 2 -8 9 9 D Q 4 6 4 3 5 4 H 5 _ P A C T G C A A C A C C A A G T G T C A A A C T C C JO E /B H Q 1 8 6 5 -8 8 9 H 5 N 1 B _ F G A T C C T C A A C T C A C T C T T C G A 7 1 7 -7 3 7 B _ R C T C T T C T G G T G A T A A T C G G T G 1 2 1 N S 8 3 7 -8 1 7 JN 9 9 2 7 9 5 B _ P A C A T T C A A A G C C A A T T C G A G C A G C T C F R 6 1 0 /B H Q 2 7 5 3 -7 7 7 B N 1 _ F T A A G A C C T T G C T T C T G G G T T 1 2 5 3 -1 2 7 2 N 1 _ R G A C C A A C C C A C A G T G T C 1 1 4 N A 1 3 6 7 -1 3 5 1 F J9 8 4 3 8 6 N 1 _ P G C A G C A T A T C C T T T T G T G G T G T C F R 6 1 0 /B H Q 2 1 3 2 1 -1 3 4 2 (H 1 N 1 )p d m 0 9 N 1 (H 5 )_ F A G T T G G T T G A C A A T T G G A A T T T 5 0 5 -5 2 6 N 1 (H 5 )_ R T T A C A C A T G C A C A T T C A G A C T 1 3 8 N A 6 4 3 -6 2 3 D Q 4 6 4 3 5 5 N 1 (H 5 )_ P G C A T A A T A A C A G A C A C C A T C A A G A G T T G G A G G A C F R 6 1 0 /B H Q 2 5 8 7 -6 0 1 H 5 N 1 N 2 _ F C C T T T G A T G A T G G A A A T G A C G 1 0 5 8 -1 0 7 8 N 2 _ R C T G T C A A C T A T G A C T T G C C T 1 4 1 N A 1 1 9 9 -1 1 8 0 C Y 0 8 1 4 2 9 N 2 _ P A A A G T C A T T G rA G G C T G G T C C A A m C JO E /B H Q 1 1 1 3 1 -1 1 5 5 H 3 N 2 H A = h ae m ag g lu ti n in ; N A = n eu ra m in id as e; N S = n o n st ru ct u ra l p ro te in ; F = fo rw ar d p ri m er ; R = re v er se p ri m er ; P = p ro b e; r = A , G ; m = A , C ; C F R 6 1 0 = C al if o rn ia F lu o r R ed 6 1 0 , B H Q = B la ck H o le Q u en ch er designed according to all basic rules [18, 23], using PrimerQuestSM (Integrated DNA Technologies, Inc. http:// eu.idtdna.com/Scitools/Applications/Primerquest/Advanced. aspx) and |