apc a Search Results


anti-rat-apc-a antibody  (Becton Dickinson)
90
Becton Dickinson anti-rat-apc-a antibody
Anti Rat Apc A Antibody, supplied by Becton Dickinson, 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/apc+a/pm22640926-301-21-23?v=Becton+Dickinson
Average 90 stars, based on 1 article reviews
anti-rat-apc-a antibody - by Bioz Stars, 2026-07
90/100 stars
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apc-a filters  (Becton Dickinson)
90
Becton Dickinson apc-a filters
Apc A Filters, supplied by Becton Dickinson, 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/apc+a/pm28124402-204-2-4?v=Becton+Dickinson
Average 90 stars, based on 1 article reviews
apc-a filters - by Bioz Stars, 2026-07
90/100 stars
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apc-a signal jf 646  (Becton Dickinson)
90
Becton Dickinson apc-a signal jf 646
(A) RT-qPCR of TFIIB normalized to 18S RNA harvested from reactivated TRExRTA BCBL-1 cells at the given timepoints. **** P < 000.1, *** P = 0.0008; one-way ANOVA with Tukey multiple comparison test. (B) Western analysis of endogenous TFIIB in TRExRTA BCBL-1 cells or (C) iSLK-KSHV(+) BAC16 cells at timepoints post-reactivation or mock. KSHV SOX is an early gene and vinculin, and GAPDH probed with mouse is a loading control. * P = 0.01636; Student’s t-test. (D) As in (A) but in iSLK-KSHV(+) BAC16 cells. (E) Flow analysis of iSLK-KSHV(+) BAC16 cells transduced with Halo or TFIIB-Halo and mock or 48 h reactivation with doxycycline (dox) and sodium butyrate; Halo was labeled with JF646-Halo dye and measured by signal in <t>the</t> <t>APC-A</t> channel. Fluorescence distributions are shown for a representative replicate and mean APC-A quantification for all samples is shown on the right. ns-nonsignificant, ** P = 0.0057; One-way ANOVA with Tukey multiple comparison test. (F) Confocal microscopy of iSLK-KSHV(+) BAC16 cells transduced with Halo protein or TFIIB-Halo, +/-viral reactivation. Hoescht 3342 delineates nuclei. Scale bar = 20 μm.
Apc A Signal Jf 646, supplied by Becton Dickinson, 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/apc+a/bio_rxiv__2024__01__16__575933-247-0-12?v=Becton+Dickinson
Average 90 stars, based on 1 article reviews
apc-a signal jf 646 - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier
second antibody reagents and isotype controls tagged with fluorochromes including allophycocyanin (apc)-a  (Becton Dickinson)
90
Becton Dickinson second antibody reagents and isotype controls tagged with fluorochromes including allophycocyanin (apc)-a
(A) RT-qPCR of TFIIB normalized to 18S RNA harvested from reactivated TRExRTA BCBL-1 cells at the given timepoints. **** P < 000.1, *** P = 0.0008; one-way ANOVA with Tukey multiple comparison test. (B) Western analysis of endogenous TFIIB in TRExRTA BCBL-1 cells or (C) iSLK-KSHV(+) BAC16 cells at timepoints post-reactivation or mock. KSHV SOX is an early gene and vinculin, and GAPDH probed with mouse is a loading control. * P = 0.01636; Student’s t-test. (D) As in (A) but in iSLK-KSHV(+) BAC16 cells. (E) Flow analysis of iSLK-KSHV(+) BAC16 cells transduced with Halo or TFIIB-Halo and mock or 48 h reactivation with doxycycline (dox) and sodium butyrate; Halo was labeled with JF646-Halo dye and measured by signal in <t>the</t> <t>APC-A</t> channel. Fluorescence distributions are shown for a representative replicate and mean APC-A quantification for all samples is shown on the right. ns-nonsignificant, ** P = 0.0057; One-way ANOVA with Tukey multiple comparison test. (F) Confocal microscopy of iSLK-KSHV(+) BAC16 cells transduced with Halo protein or TFIIB-Halo, +/-viral reactivation. Hoescht 3342 delineates nuclei. Scale bar = 20 μm.
Second Antibody Reagents And Isotype Controls Tagged With Fluorochromes Including Allophycocyanin (Apc) A, supplied by Becton Dickinson, 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/apc+a/pm19074419-48-24-35?v=Becton+Dickinson
Average 90 stars, based on 1 article reviews
second antibody reagents and isotype controls tagged with fluorochromes including allophycocyanin (apc)-a - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier

Image Search Results


(A) RT-qPCR of TFIIB normalized to 18S RNA harvested from reactivated TRExRTA BCBL-1 cells at the given timepoints. **** P < 000.1, *** P = 0.0008; one-way ANOVA with Tukey multiple comparison test. (B) Western analysis of endogenous TFIIB in TRExRTA BCBL-1 cells or (C) iSLK-KSHV(+) BAC16 cells at timepoints post-reactivation or mock. KSHV SOX is an early gene and vinculin, and GAPDH probed with mouse is a loading control. * P = 0.01636; Student’s t-test. (D) As in (A) but in iSLK-KSHV(+) BAC16 cells. (E) Flow analysis of iSLK-KSHV(+) BAC16 cells transduced with Halo or TFIIB-Halo and mock or 48 h reactivation with doxycycline (dox) and sodium butyrate; Halo was labeled with JF646-Halo dye and measured by signal in the APC-A channel. Fluorescence distributions are shown for a representative replicate and mean APC-A quantification for all samples is shown on the right. ns-nonsignificant, ** P = 0.0057; One-way ANOVA with Tukey multiple comparison test. (F) Confocal microscopy of iSLK-KSHV(+) BAC16 cells transduced with Halo protein or TFIIB-Halo, +/-viral reactivation. Hoescht 3342 delineates nuclei. Scale bar = 20 μm.

Journal: bioRxiv

Article Title: The RNA polymerase II general transcription factor TFIIB is a target for transcriptome control during cellular stress and viral infection

doi: 10.1101/2024.01.16.575933

Figure Lengend Snippet: (A) RT-qPCR of TFIIB normalized to 18S RNA harvested from reactivated TRExRTA BCBL-1 cells at the given timepoints. **** P < 000.1, *** P = 0.0008; one-way ANOVA with Tukey multiple comparison test. (B) Western analysis of endogenous TFIIB in TRExRTA BCBL-1 cells or (C) iSLK-KSHV(+) BAC16 cells at timepoints post-reactivation or mock. KSHV SOX is an early gene and vinculin, and GAPDH probed with mouse is a loading control. * P = 0.01636; Student’s t-test. (D) As in (A) but in iSLK-KSHV(+) BAC16 cells. (E) Flow analysis of iSLK-KSHV(+) BAC16 cells transduced with Halo or TFIIB-Halo and mock or 48 h reactivation with doxycycline (dox) and sodium butyrate; Halo was labeled with JF646-Halo dye and measured by signal in the APC-A channel. Fluorescence distributions are shown for a representative replicate and mean APC-A quantification for all samples is shown on the right. ns-nonsignificant, ** P = 0.0057; One-way ANOVA with Tukey multiple comparison test. (F) Confocal microscopy of iSLK-KSHV(+) BAC16 cells transduced with Halo protein or TFIIB-Halo, +/-viral reactivation. Hoescht 3342 delineates nuclei. Scale bar = 20 μm.

Article Snippet: APC-A signal (for JF 646) was quantified by flow cytometry on a BD Bioscience LSR Fortessa.

Techniques: Quantitative RT-PCR, Comparison, Western Blot, Transduction, Labeling, Fluorescence, Confocal Microscopy

(A) Western blotting of iSLK cells containing or lacking the KSHV BAC16. Cells were mock treated or dosed with 5 ug/mL doxycycline (Dox) and 1 mM sodium butyrate (NaBut) for 48 h. KSHV SOX is a marker for lytic viral infection and anti-GAPDH probed with rabbit antibody is a loading control. ( B) Flow analysis of iSLK cells expressing TFIIB-Halo and containing or lacking the KSHV BAC16. Cells were treated with Dox and NaBut and harvested 48h later. Halo was labeled with JF646-Halo dye and was measured by the signal in the APC-A channel and the fold change in fluorescence over mock-treated cells was quantified. *P < 0.0307; Student’s unpaired t-test.

Journal: bioRxiv

Article Title: The RNA polymerase II general transcription factor TFIIB is a target for transcriptome control during cellular stress and viral infection

doi: 10.1101/2024.01.16.575933

Figure Lengend Snippet: (A) Western blotting of iSLK cells containing or lacking the KSHV BAC16. Cells were mock treated or dosed with 5 ug/mL doxycycline (Dox) and 1 mM sodium butyrate (NaBut) for 48 h. KSHV SOX is a marker for lytic viral infection and anti-GAPDH probed with rabbit antibody is a loading control. ( B) Flow analysis of iSLK cells expressing TFIIB-Halo and containing or lacking the KSHV BAC16. Cells were treated with Dox and NaBut and harvested 48h later. Halo was labeled with JF646-Halo dye and was measured by the signal in the APC-A channel and the fold change in fluorescence over mock-treated cells was quantified. *P < 0.0307; Student’s unpaired t-test.

Article Snippet: APC-A signal (for JF 646) was quantified by flow cytometry on a BD Bioscience LSR Fortessa.

Techniques: Western Blot, Marker, Infection, Expressing, Labeling, Fluorescence