v dia strain 122 Search Results


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Celera celera sequencing strain
Transposons, piRNAs, and piRNA precursors in zucchini and squash mutant ovaries. (A) Transcripts of gypsy, idefix, and ZAM transposons were detected by qPCR. (B) Individual piRNAs targeting gypsy and idefix were detected by qPCR. (C) Piwi protein levels in mutant and heterozygous ovary extracts were measured by Western blotting. Tubulin serves as loading control. Celera sequencing strain (S-strain) is shown in addition. (D) Three ∼100-nt regions of flamenco that are normally highly processed into piRNAs were detected by qPCR. The positions of these segments are indicated in Figure 4. qPCR data were normalized to internal controls rp49 (A,C) or bantam (B). Fold changes relative to heterozygous siblings are shown on a linear scale. Error bars represent one standard deviation over three technical replicates.
Celera Sequencing Strain, supplied by Celera, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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DSMZ dsmz strain 877
Transposons, piRNAs, and piRNA precursors in zucchini and squash mutant ovaries. (A) Transcripts of gypsy, idefix, and ZAM transposons were detected by qPCR. (B) Individual piRNAs targeting gypsy and idefix were detected by qPCR. (C) Piwi protein levels in mutant and heterozygous ovary extracts were measured by Western blotting. Tubulin serves as loading control. Celera sequencing strain (S-strain) is shown in addition. (D) Three ∼100-nt regions of flamenco that are normally highly processed into piRNAs were detected by qPCR. The positions of these segments are indicated in Figure 4. qPCR data were normalized to internal controls rp49 (A,C) or bantam (B). Fold changes relative to heterozygous siblings are shown on a linear scale. Error bars represent one standard deviation over three technical replicates.
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Sanofi bacterial strains e. cloacae
Transposons, piRNAs, and piRNA precursors in zucchini and squash mutant ovaries. (A) Transcripts of gypsy, idefix, and ZAM transposons were detected by qPCR. (B) Individual piRNAs targeting gypsy and idefix were detected by qPCR. (C) Piwi protein levels in mutant and heterozygous ovary extracts were measured by Western blotting. Tubulin serves as loading control. Celera sequencing strain (S-strain) is shown in addition. (D) Three ∼100-nt regions of flamenco that are normally highly processed into piRNAs were detected by qPCR. The positions of these segments are indicated in Figure 4. qPCR data were normalized to internal controls rp49 (A,C) or bantam (B). Fold changes relative to heterozygous siblings are shown on a linear scale. Error bars represent one standard deviation over three technical replicates.
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Pasteur Institute bacterial strains
Transposons, piRNAs, and piRNA precursors in zucchini and squash mutant ovaries. (A) Transcripts of gypsy, idefix, and ZAM transposons were detected by qPCR. (B) Individual piRNAs targeting gypsy and idefix were detected by qPCR. (C) Piwi protein levels in mutant and heterozygous ovary extracts were measured by Western blotting. Tubulin serves as loading control. Celera sequencing strain (S-strain) is shown in addition. (D) Three ∼100-nt regions of flamenco that are normally highly processed into piRNAs were detected by qPCR. The positions of these segments are indicated in Figure 4. qPCR data were normalized to internal controls rp49 (A,C) or bantam (B). Fold changes relative to heterozygous siblings are shown on a linear scale. Error bars represent one standard deviation over three technical replicates.
Bacterial Strains, supplied by Pasteur Institute, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Transposons, piRNAs, and piRNA precursors in zucchini and squash mutant ovaries. (A) Transcripts of gypsy, idefix, and ZAM transposons were detected by qPCR. (B) Individual piRNAs targeting gypsy and idefix were detected by qPCR. (C) Piwi protein levels in mutant and heterozygous ovary extracts were measured by Western blotting. Tubulin serves as loading control. Celera sequencing strain (S-strain) is shown in addition. (D) Three ∼100-nt regions of flamenco that are normally highly processed into piRNAs were detected by qPCR. The positions of these segments are indicated in Figure 4. qPCR data were normalized to internal controls rp49 (A,C) or bantam (B). Fold changes relative to heterozygous siblings are shown on a linear scale. Error bars represent one standard deviation over three technical replicates.

Journal: Genes & Development

Article Title: Probing the initiation and effector phases of the somatic piRNA pathway in Drosophila

doi: 10.1101/gad.1968110

Figure Lengend Snippet: Transposons, piRNAs, and piRNA precursors in zucchini and squash mutant ovaries. (A) Transcripts of gypsy, idefix, and ZAM transposons were detected by qPCR. (B) Individual piRNAs targeting gypsy and idefix were detected by qPCR. (C) Piwi protein levels in mutant and heterozygous ovary extracts were measured by Western blotting. Tubulin serves as loading control. Celera sequencing strain (S-strain) is shown in addition. (D) Three ∼100-nt regions of flamenco that are normally highly processed into piRNAs were detected by qPCR. The positions of these segments are indicated in Figure 4. qPCR data were normalized to internal controls rp49 (A,C) or bantam (B). Fold changes relative to heterozygous siblings are shown on a linear scale. Error bars represent one standard deviation over three technical replicates.

Article Snippet: Celera sequencing strain (S-strain) is shown in addition. ( D ) Three ∼100-nt regions of flamenco that are normally highly processed into piRNAs were detected by qPCR.

Techniques: Mutagenesis, Western Blot, Sequencing, Standard Deviation