cdna cloning primer Search Results


94
Danaher Inc cdna cloning primer
FIGURE 3. Engineering a full-length PHR1 <t>cDNA.</t> Indicated by thin black lines are products generated <t>by</t> <t>5-RACE,</t> 3-RACE, and RT-PCR that were used to form the full-length PHR1 cDNA. An N-terminal cassette was formed by joining products A and B using a NotI site. A C-terminal cassette was formed by joining products G, H, and F using SphI and EagI. The N- and C-terminal cassettes were joined to form the full-length PHR1 cDNA using a unique (*) SmaI site.
Cdna Cloning Primer, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/cdna cloning primer/product/Danaher Inc
Average 94 stars, based on 1 article reviews
cdna cloning primer - by Bioz Stars, 2026-06
94/100 stars
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90
Gallus BioPharmaceuticals dna primers based on the sequence of a cdna clone of gallus gallus cytoplasmic -actin
FIGURE 3. Engineering a full-length PHR1 <t>cDNA.</t> Indicated by thin black lines are products generated <t>by</t> <t>5-RACE,</t> 3-RACE, and RT-PCR that were used to form the full-length PHR1 cDNA. An N-terminal cassette was formed by joining products A and B using a NotI site. A C-terminal cassette was formed by joining products G, H, and F using SphI and EagI. The N- and C-terminal cassettes were joined to form the full-length PHR1 cDNA using a unique (*) SmaI site.
Dna Primers Based On The Sequence Of A Cdna Clone Of Gallus Gallus Cytoplasmic Actin, supplied by Gallus BioPharmaceuticals, 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/result/dna primers based on the sequence of a cdna clone of gallus gallus cytoplasmic -actin/product/Gallus BioPharmaceuticals
Average 90 stars, based on 1 article reviews
dna primers based on the sequence of a cdna clone of gallus gallus cytoplasmic -actin - by Bioz Stars, 2026-06
90/100 stars
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90
Clonegene cdna clone gene speciwc sense primers
FIGURE 3. Engineering a full-length PHR1 <t>cDNA.</t> Indicated by thin black lines are products generated <t>by</t> <t>5-RACE,</t> 3-RACE, and RT-PCR that were used to form the full-length PHR1 cDNA. An N-terminal cassette was formed by joining products A and B using a NotI site. A C-terminal cassette was formed by joining products G, H, and F using SphI and EagI. The N- and C-terminal cassettes were joined to form the full-length PHR1 cDNA using a unique (*) SmaI site.
Cdna Clone Gene Speciwc Sense Primers, supplied by Clonegene, 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/result/cdna clone gene speciwc sense primers/product/Clonegene
Average 90 stars, based on 1 article reviews
cdna clone gene speciwc sense primers - by Bioz Stars, 2026-06
90/100 stars
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90
TIB MOLBIOL primers for pcr cloning and cdna sequencing
FIGURE 3. Engineering a full-length PHR1 <t>cDNA.</t> Indicated by thin black lines are products generated <t>by</t> <t>5-RACE,</t> 3-RACE, and RT-PCR that were used to form the full-length PHR1 cDNA. An N-terminal cassette was formed by joining products A and B using a NotI site. A C-terminal cassette was formed by joining products G, H, and F using SphI and EagI. The N- and C-terminal cassettes were joined to form the full-length PHR1 cDNA using a unique (*) SmaI site.
Primers For Pcr Cloning And Cdna Sequencing, supplied by TIB MOLBIOL, 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/result/primers for pcr cloning and cdna sequencing/product/TIB MOLBIOL
Average 90 stars, based on 1 article reviews
primers for pcr cloning and cdna sequencing - by Bioz Stars, 2026-06
90/100 stars
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Image Search Results


FIGURE 3. Engineering a full-length PHR1 cDNA. Indicated by thin black lines are products generated by 5-RACE, 3-RACE, and RT-PCR that were used to form the full-length PHR1 cDNA. An N-terminal cassette was formed by joining products A and B using a NotI site. A C-terminal cassette was formed by joining products G, H, and F using SphI and EagI. The N- and C-terminal cassettes were joined to form the full-length PHR1 cDNA using a unique (*) SmaI site.

Journal: Journal of Biological Chemistry

Article Title: Critical Role of 7,8-Didemethyl-8-hydroxy-5-deazariboflavin for Photoreactivation in Chlamydomonas reinhardtii

doi: 10.1074/jbc.m110.146050

Figure Lengend Snippet: FIGURE 3. Engineering a full-length PHR1 cDNA. Indicated by thin black lines are products generated by 5-RACE, 3-RACE, and RT-PCR that were used to form the full-length PHR1 cDNA. An N-terminal cassette was formed by joining products A and B using a NotI site. A C-terminal cassette was formed by joining products G, H, and F using SphI and EagI. The N- and C-terminal cassettes were joined to form the full-length PHR1 cDNA using a unique (*) SmaI site.

Article Snippet: 3 -RACE—Poly(A)RNA fromChlamydomonas strain cc-125 was reverse-transcribed using cDNA cloning primer (Integrated DNA Technologies) and ImProm-II reverse transcriptase (Promega).

Techniques: Generated, Reverse Transcription Polymerase Chain Reaction