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MCLAB Inc barcoding mix
Barcoding Mix, supplied by MCLAB Inc, 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/barcoding mix/product/MCLAB Inc
Average 90 stars, based on 1 article reviews
barcoding mix - by Bioz Stars, 2026-05
90/100 stars

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Image Search Results


Journal: bioRxiv

Article Title: Optimising the use of Oxford nanopore sequencing technology for detection of Wolbachia bacterial endosymbionts in Anopheles mosquitoes

doi: 10.1101/2025.06.16.659891

Figure Lengend Snippet:

Article Snippet: Extracted gDNA from individual mosquitoes was prepared by diluting 10ng of DNA in 15μL of nuclease free water and then the diluted DNA was combined with NEB LongAmp Taq 2x master mix and respective 16S barcodes.

Techniques: Sequencing

All bar graphs depict sequencing runs using two different barcoding kits: the Rapid PCR Barcoding Kit 24 V14 (runs 2-6) and the 16S Barcoding Kit 24 V14 (runs 7,8,9,11,12). Each run is represented by a vertical column. A ) Total Data generated (GB). B ) Percentage of passed vs failed bases called for each run. C ) Total number of reads obtained in each sequencing run. D ) Percentage of unclassified passed reads and unclassified passed bases for each run.

Journal: bioRxiv

Article Title: Optimising the use of Oxford nanopore sequencing technology for detection of Wolbachia bacterial endosymbionts in Anopheles mosquitoes

doi: 10.1101/2025.06.16.659891

Figure Lengend Snippet: All bar graphs depict sequencing runs using two different barcoding kits: the Rapid PCR Barcoding Kit 24 V14 (runs 2-6) and the 16S Barcoding Kit 24 V14 (runs 7,8,9,11,12). Each run is represented by a vertical column. A ) Total Data generated (GB). B ) Percentage of passed vs failed bases called for each run. C ) Total number of reads obtained in each sequencing run. D ) Percentage of unclassified passed reads and unclassified passed bases for each run.

Article Snippet: Extracted gDNA from individual mosquitoes was prepared by diluting 10ng of DNA in 15μL of nuclease free water and then the diluted DNA was combined with NEB LongAmp Taq 2x master mix and respective 16S barcodes.

Techniques: Sequencing, Generated

Libraries prepared and sequenced using either the Rapid PCR Barcoding Kit 24 V14 (Rapid) or 16S Barcoding Kit 24 V14 (16S).

Journal: bioRxiv

Article Title: Optimising the use of Oxford nanopore sequencing technology for detection of Wolbachia bacterial endosymbionts in Anopheles mosquitoes

doi: 10.1101/2025.06.16.659891

Figure Lengend Snippet: Libraries prepared and sequenced using either the Rapid PCR Barcoding Kit 24 V14 (Rapid) or 16S Barcoding Kit 24 V14 (16S).

Article Snippet: Extracted gDNA from individual mosquitoes was prepared by diluting 10ng of DNA in 15μL of nuclease free water and then the diluted DNA was combined with NEB LongAmp Taq 2x master mix and respective 16S barcodes.

Techniques:

Antibodies for CyTOF.

Journal: Frontiers in Immunology

Article Title: The gut-brain-axis one year after treatment with cladribine tablets in patients with relapsing remitting multiple sclerosis: a pilot study

doi: 10.3389/fimmu.2025.1514762

Figure Lengend Snippet: Antibodies for CyTOF.

Article Snippet: We first barcoded the samples using CD45 barcoding mixes (Standard BioTools).

Techniques:

Different repopulation of various immune cells after cladribine treatment. (A) UMAP plot displaying CD45 + immune cells from the blood of cladribine-treated patients at different time points. Colors correspond to PARC-guided clustering. (B) Density UMAP plots showing the proportion of cells assigned to each time point according to each cluster. Color key indicates high (red) and low (blue) percentage of immune cells. (C) Percentage of each annotated cell population out of the total CD45 + immune cells at each time point. Each data point corresponds to each individual, colored by time point. Significant P-values are stated in the graphs. D0: baseline visit; M3: 3 month visit; M12: 12 month visit.

Journal: Frontiers in Immunology

Article Title: The gut-brain-axis one year after treatment with cladribine tablets in patients with relapsing remitting multiple sclerosis: a pilot study

doi: 10.3389/fimmu.2025.1514762

Figure Lengend Snippet: Different repopulation of various immune cells after cladribine treatment. (A) UMAP plot displaying CD45 + immune cells from the blood of cladribine-treated patients at different time points. Colors correspond to PARC-guided clustering. (B) Density UMAP plots showing the proportion of cells assigned to each time point according to each cluster. Color key indicates high (red) and low (blue) percentage of immune cells. (C) Percentage of each annotated cell population out of the total CD45 + immune cells at each time point. Each data point corresponds to each individual, colored by time point. Significant P-values are stated in the graphs. D0: baseline visit; M3: 3 month visit; M12: 12 month visit.

Article Snippet: We first barcoded the samples using CD45 barcoding mixes (Standard BioTools).

Techniques: