Difference between revisions of "Part:BBa K4897001"
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<partinfo>BBa_K4897001 short</partinfo> | <partinfo>BBa_K4897001 short</partinfo> | ||
− | BS DNA- | + | BS DNA-162 was designed by BS United China as a single-stranded DNA segment complementary to the 131 base pairs of the 16S rRNA gene of P. acne. The composition of the DNA has three categories: binding region (two ends), amplification region, and random region. The binding region is the key element in reacting with the P. acne 16s rRNA gene. The DNA ligase will perform the ligation of the single-stranded DNA meanwhile the phi29 will generate double-stranded DNA through amplification primers |
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===Usage and Biology=== | ===Usage and Biology=== | ||
+ | BS DNA-162 would bind the bacterial DNA of P. acne and show great sensitivity and specificity. | ||
− | |||
<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> | ||
<partinfo>BBa_K4897001 SequenceAndFeatures</partinfo> | <partinfo>BBa_K4897001 SequenceAndFeatures</partinfo> | ||
+ | |||
+ | ===Characterization=== | ||
Revision as of 10:45, 7 October 2023
BS DNA-162 (BS DNA 2.0) using in L-RCA for detecting P. acne
BS DNA-162 was designed by BS United China as a single-stranded DNA segment complementary to the 131 base pairs of the 16S rRNA gene of P. acne. The composition of the DNA has three categories: binding region (two ends), amplification region, and random region. The binding region is the key element in reacting with the P. acne 16s rRNA gene. The DNA ligase will perform the ligation of the single-stranded DNA meanwhile the phi29 will generate double-stranded DNA through amplification primers
Usage and Biology
BS DNA-162 would bind the bacterial DNA of P. acne and show great sensitivity and specificity.
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal SpeI site found at 83
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 57
Illegal SpeI site found at 83 - 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 68
- 23INCOMPATIBLE WITH RFC[23]Illegal SpeI site found at 83
- 25INCOMPATIBLE WITH RFC[25]Illegal SpeI site found at 83
- 1000COMPATIBLE WITH RFC[1000]