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DuPont de Nemours macro-enabled excel tool
Macro Enabled Excel Tool, supplied by DuPont de Nemours, 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/macro-enabled+excel+tool/pmc08328194-120-12-17?v=DuPont+de+Nemours
Average 90 stars, based on 1 article reviews
macro-enabled excel tool - by Bioz Stars, 2026-08
90/100 stars

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DuPont de Nemours macro-enabled excel tool
Macro Enabled Excel Tool, supplied by DuPont de Nemours, 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/macro-enabled+excel+tool/pmc08328194-120-12-17?v=DuPont+de+Nemours
Average 90 stars, based on 1 article reviews
macro-enabled excel tool - by Bioz Stars, 2026-08
90/100 stars
  Buy from Supplier

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DuPont de Nemours macro-enabled excel tool crispr database ii
Genetic organization of the CRISPR1- cas locus in Streptococcus agalactiae . cas genes and core genes are shown as black arrows and blue arrows, respectively. The leader sequence is located between the cas gene cluster and the <t>CRISPR</t> array (white box; L) while the trailer sequence is located downstream of the array (white box; T). The direct repeats (DR) are shown as black diamonds and the terminal repeat, which differs from the consensus DR, is shown as a white diamond. Spacers are shown as colored rectangles and unique spacers are represented by unique colors. Below the CRISPR array, the sequence of the first two repeat-spacer units is shown with the DRs in black characters and the spacers in color characters.
Macro Enabled Excel Tool Crispr Database Ii, supplied by DuPont de Nemours, 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/macro-enabled+excel+tool/pmc04466440-120-12-21?v=DuPont+de+Nemours
Average 90 stars, based on 1 article reviews
macro-enabled excel tool crispr database ii - by Bioz Stars, 2026-08
90/100 stars
  Buy from Supplier

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Genetic organization of the CRISPR1- cas locus in Streptococcus agalactiae . cas genes and core genes are shown as black arrows and blue arrows, respectively. The leader sequence is located between the cas gene cluster and the CRISPR array (white box; L) while the trailer sequence is located downstream of the array (white box; T). The direct repeats (DR) are shown as black diamonds and the terminal repeat, which differs from the consensus DR, is shown as a white diamond. Spacers are shown as colored rectangles and unique spacers are represented by unique colors. Below the CRISPR array, the sequence of the first two repeat-spacer units is shown with the DRs in black characters and the spacers in color characters.

Journal: Frontiers in Genetics

Article Title: Analysis of the type II-A CRISPR-Cas system of Streptococcus agalactiae reveals distinctive features according to genetic lineages

doi: 10.3389/fgene.2015.00214

Figure Lengend Snippet: Genetic organization of the CRISPR1- cas locus in Streptococcus agalactiae . cas genes and core genes are shown as black arrows and blue arrows, respectively. The leader sequence is located between the cas gene cluster and the CRISPR array (white box; L) while the trailer sequence is located downstream of the array (white box; T). The direct repeats (DR) are shown as black diamonds and the terminal repeat, which differs from the consensus DR, is shown as a white diamond. Spacers are shown as colored rectangles and unique spacers are represented by unique colors. Below the CRISPR array, the sequence of the first two repeat-spacer units is shown with the DRs in black characters and the spacers in color characters.

Article Snippet: In a second step, CRISPR1 array structure was determined anew using a macro-enabled Excel tool named CRISPR database II (P. Horvath, DuPont) that comprises different programs for the identification and extraction of CRISPR features in nucleotide sequences, and for subsequently establishing a graphic representation of spacer diversity.

Techniques: Sequencing, CRISPR