Catalog Number Search Results


91
Revvity polyscreen pvdf hybridization transfer membrane
(A) Endogenous PDPK1 was recovered from lysates of the indicated cell lines and probed for co-precipitating WDR5 by IB. Inputs for PDPK1 are 10%–20%. Inputs for WDR5 are 1%–5%. n = 3 biological replicates. (B) Proximity ligation assay with FLAG and WDR5 antibodies in U2OS cells stably expressing FLAG-tagged PDPK1. Cells were treated overnight (30 μM C6/C6nc) before analysis; scale bar, 20 μm. n = 3 biological replicates. (C) HEK293 cells were treated overnight with 30 μM C6 or 5 μM GSK470, lysates prepared, and a PDPK1 IP performed. IB was then performed for the indicated proteins. Inputs are 5% for PDPK1 and 1% for all others. n = 3 biological replicates. (D) HEK293 cells were fractionated into cytosolic (S2), soluble nuclear (S3), and chromatin-associated (P3) fractions. Equal amounts of each fraction were analyzed by IB with the antibodies against the indicated proteins. H3 (nuclear) and α-tubulin (cytosolic) are controls for fractionation. n = 3 biological replicates. (E) Cytosolic and nuclear lysates from HEK293 cells were subject to IP with PDPK1 antibody or an IgG control and immunoblotted with antibodies against the indicated proteins. A short and long exposure of the WDR5 IB are shown. n = 3 biological replicates. (F) PDPK1 possesses two WIN-like motifs centered on R3 and R238. (G) FLAG-tagged PDPK1 (WT and the R3A and R238A mutants) were transiently expressed in HEK293 cells; lysates were prepared and subject to IP with anti-FLAG beads. Immune complexes were probed for PDPK1 or endogenous WDR5 by IB. n = 3 biological replicates. (H) FLAG-tagged PDPK1 (WT and the R3A) was transiently expressed in HEK293 cells, recovered by FLAG-IP, resolved by SDS-PAGE, and transferred to polyvinylidene fluoride <t>(PVDF)</t> membrane. Membranes were then incubated with recombinant WDR5 followed by anti-WDR5 antibody. n = 3 biological replicates. (I) In vitro -transcribed and -translated PDPK1-FLAG variants were incubated with recombinant 6xHis-SUMO-WDR5 proteins, recovered with Ni-NTA agarose, and analyzed by IB. n = 2 biological replicates. PH, pleckstrin homology domain. See also .
Polyscreen Pvdf Hybridization Transfer Membrane, supplied by Revvity, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/polyscreen pvdf hybridization transfer membrane/product/Revvity
Average 91 stars, based on 1 article reviews
polyscreen pvdf hybridization transfer membrane - by Bioz Stars, 2026-04
91/100 stars
  Buy from Supplier

88
Revvity polyscreen polyvinylidene difluoride transfer membrane
(A) Endogenous PDPK1 was recovered from lysates of the indicated cell lines and probed for co-precipitating WDR5 by IB. Inputs for PDPK1 are 10%–20%. Inputs for WDR5 are 1%–5%. n = 3 biological replicates. (B) Proximity ligation assay with FLAG and WDR5 antibodies in U2OS cells stably expressing FLAG-tagged PDPK1. Cells were treated overnight (30 μM C6/C6nc) before analysis; scale bar, 20 μm. n = 3 biological replicates. (C) HEK293 cells were treated overnight with 30 μM C6 or 5 μM GSK470, lysates prepared, and a PDPK1 IP performed. IB was then performed for the indicated proteins. Inputs are 5% for PDPK1 and 1% for all others. n = 3 biological replicates. (D) HEK293 cells were fractionated into cytosolic (S2), soluble nuclear (S3), and chromatin-associated (P3) fractions. Equal amounts of each fraction were analyzed by IB with the antibodies against the indicated proteins. H3 (nuclear) and α-tubulin (cytosolic) are controls for fractionation. n = 3 biological replicates. (E) Cytosolic and nuclear lysates from HEK293 cells were subject to IP with PDPK1 antibody or an IgG control and immunoblotted with antibodies against the indicated proteins. A short and long exposure of the WDR5 IB are shown. n = 3 biological replicates. (F) PDPK1 possesses two WIN-like motifs centered on R3 and R238. (G) FLAG-tagged PDPK1 (WT and the R3A and R238A mutants) were transiently expressed in HEK293 cells; lysates were prepared and subject to IP with anti-FLAG beads. Immune complexes were probed for PDPK1 or endogenous WDR5 by IB. n = 3 biological replicates. (H) FLAG-tagged PDPK1 (WT and the R3A) was transiently expressed in HEK293 cells, recovered by FLAG-IP, resolved by SDS-PAGE, and transferred to polyvinylidene fluoride <t>(PVDF)</t> membrane. Membranes were then incubated with recombinant WDR5 followed by anti-WDR5 antibody. n = 3 biological replicates. (I) In vitro -transcribed and -translated PDPK1-FLAG variants were incubated with recombinant 6xHis-SUMO-WDR5 proteins, recovered with Ni-NTA agarose, and analyzed by IB. n = 2 biological replicates. PH, pleckstrin homology domain. See also .
Polyscreen Polyvinylidene Difluoride Transfer Membrane, supplied by Revvity, used in various techniques. Bioz Stars score: 88/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/polyscreen polyvinylidene difluoride transfer membrane/product/Revvity
Average 88 stars, based on 1 article reviews
polyscreen polyvinylidene difluoride transfer membrane - by Bioz Stars, 2026-04
88/100 stars
  Buy from Supplier

90
Corning Life Sciences polypropylene tubes #352070
(A) Endogenous PDPK1 was recovered from lysates of the indicated cell lines and probed for co-precipitating WDR5 by IB. Inputs for PDPK1 are 10%–20%. Inputs for WDR5 are 1%–5%. n = 3 biological replicates. (B) Proximity ligation assay with FLAG and WDR5 antibodies in U2OS cells stably expressing FLAG-tagged PDPK1. Cells were treated overnight (30 μM C6/C6nc) before analysis; scale bar, 20 μm. n = 3 biological replicates. (C) HEK293 cells were treated overnight with 30 μM C6 or 5 μM GSK470, lysates prepared, and a PDPK1 IP performed. IB was then performed for the indicated proteins. Inputs are 5% for PDPK1 and 1% for all others. n = 3 biological replicates. (D) HEK293 cells were fractionated into cytosolic (S2), soluble nuclear (S3), and chromatin-associated (P3) fractions. Equal amounts of each fraction were analyzed by IB with the antibodies against the indicated proteins. H3 (nuclear) and α-tubulin (cytosolic) are controls for fractionation. n = 3 biological replicates. (E) Cytosolic and nuclear lysates from HEK293 cells were subject to IP with PDPK1 antibody or an IgG control and immunoblotted with antibodies against the indicated proteins. A short and long exposure of the WDR5 IB are shown. n = 3 biological replicates. (F) PDPK1 possesses two WIN-like motifs centered on R3 and R238. (G) FLAG-tagged PDPK1 (WT and the R3A and R238A mutants) were transiently expressed in HEK293 cells; lysates were prepared and subject to IP with anti-FLAG beads. Immune complexes were probed for PDPK1 or endogenous WDR5 by IB. n = 3 biological replicates. (H) FLAG-tagged PDPK1 (WT and the R3A) was transiently expressed in HEK293 cells, recovered by FLAG-IP, resolved by SDS-PAGE, and transferred to polyvinylidene fluoride <t>(PVDF)</t> membrane. Membranes were then incubated with recombinant WDR5 followed by anti-WDR5 antibody. n = 3 biological replicates. (I) In vitro -transcribed and -translated PDPK1-FLAG variants were incubated with recombinant 6xHis-SUMO-WDR5 proteins, recovered with Ni-NTA agarose, and analyzed by IB. n = 2 biological replicates. PH, pleckstrin homology domain. See also .
Polypropylene Tubes #352070, supplied by Corning Life Sciences, 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/polypropylene tubes #352070/product/Corning Life Sciences
Average 90 stars, based on 1 article reviews
polypropylene tubes #352070 - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

90
Geneaid Biotech Ltd loading dye hh 13,701
(A) Endogenous PDPK1 was recovered from lysates of the indicated cell lines and probed for co-precipitating WDR5 by IB. Inputs for PDPK1 are 10%–20%. Inputs for WDR5 are 1%–5%. n = 3 biological replicates. (B) Proximity ligation assay with FLAG and WDR5 antibodies in U2OS cells stably expressing FLAG-tagged PDPK1. Cells were treated overnight (30 μM C6/C6nc) before analysis; scale bar, 20 μm. n = 3 biological replicates. (C) HEK293 cells were treated overnight with 30 μM C6 or 5 μM GSK470, lysates prepared, and a PDPK1 IP performed. IB was then performed for the indicated proteins. Inputs are 5% for PDPK1 and 1% for all others. n = 3 biological replicates. (D) HEK293 cells were fractionated into cytosolic (S2), soluble nuclear (S3), and chromatin-associated (P3) fractions. Equal amounts of each fraction were analyzed by IB with the antibodies against the indicated proteins. H3 (nuclear) and α-tubulin (cytosolic) are controls for fractionation. n = 3 biological replicates. (E) Cytosolic and nuclear lysates from HEK293 cells were subject to IP with PDPK1 antibody or an IgG control and immunoblotted with antibodies against the indicated proteins. A short and long exposure of the WDR5 IB are shown. n = 3 biological replicates. (F) PDPK1 possesses two WIN-like motifs centered on R3 and R238. (G) FLAG-tagged PDPK1 (WT and the R3A and R238A mutants) were transiently expressed in HEK293 cells; lysates were prepared and subject to IP with anti-FLAG beads. Immune complexes were probed for PDPK1 or endogenous WDR5 by IB. n = 3 biological replicates. (H) FLAG-tagged PDPK1 (WT and the R3A) was transiently expressed in HEK293 cells, recovered by FLAG-IP, resolved by SDS-PAGE, and transferred to polyvinylidene fluoride <t>(PVDF)</t> membrane. Membranes were then incubated with recombinant WDR5 followed by anti-WDR5 antibody. n = 3 biological replicates. (I) In vitro -transcribed and -translated PDPK1-FLAG variants were incubated with recombinant 6xHis-SUMO-WDR5 proteins, recovered with Ni-NTA agarose, and analyzed by IB. n = 2 biological replicates. PH, pleckstrin homology domain. See also .
Loading Dye Hh 13,701, supplied by Geneaid Biotech Ltd, 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/loading dye hh 13,701/product/Geneaid Biotech Ltd
Average 90 stars, based on 1 article reviews
loading dye hh 13,701 - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

90
Fisher Scientific pre-labeled and pre-weighed sample containers fisher scientific autoclavable polypropylene biohazard sample bags, catalog number 01-826-5
(A) Endogenous PDPK1 was recovered from lysates of the indicated cell lines and probed for co-precipitating WDR5 by IB. Inputs for PDPK1 are 10%–20%. Inputs for WDR5 are 1%–5%. n = 3 biological replicates. (B) Proximity ligation assay with FLAG and WDR5 antibodies in U2OS cells stably expressing FLAG-tagged PDPK1. Cells were treated overnight (30 μM C6/C6nc) before analysis; scale bar, 20 μm. n = 3 biological replicates. (C) HEK293 cells were treated overnight with 30 μM C6 or 5 μM GSK470, lysates prepared, and a PDPK1 IP performed. IB was then performed for the indicated proteins. Inputs are 5% for PDPK1 and 1% for all others. n = 3 biological replicates. (D) HEK293 cells were fractionated into cytosolic (S2), soluble nuclear (S3), and chromatin-associated (P3) fractions. Equal amounts of each fraction were analyzed by IB with the antibodies against the indicated proteins. H3 (nuclear) and α-tubulin (cytosolic) are controls for fractionation. n = 3 biological replicates. (E) Cytosolic and nuclear lysates from HEK293 cells were subject to IP with PDPK1 antibody or an IgG control and immunoblotted with antibodies against the indicated proteins. A short and long exposure of the WDR5 IB are shown. n = 3 biological replicates. (F) PDPK1 possesses two WIN-like motifs centered on R3 and R238. (G) FLAG-tagged PDPK1 (WT and the R3A and R238A mutants) were transiently expressed in HEK293 cells; lysates were prepared and subject to IP with anti-FLAG beads. Immune complexes were probed for PDPK1 or endogenous WDR5 by IB. n = 3 biological replicates. (H) FLAG-tagged PDPK1 (WT and the R3A) was transiently expressed in HEK293 cells, recovered by FLAG-IP, resolved by SDS-PAGE, and transferred to polyvinylidene fluoride <t>(PVDF)</t> membrane. Membranes were then incubated with recombinant WDR5 followed by anti-WDR5 antibody. n = 3 biological replicates. (I) In vitro -transcribed and -translated PDPK1-FLAG variants were incubated with recombinant 6xHis-SUMO-WDR5 proteins, recovered with Ni-NTA agarose, and analyzed by IB. n = 2 biological replicates. PH, pleckstrin homology domain. See also .
Pre Labeled And Pre Weighed Sample Containers Fisher Scientific Autoclavable Polypropylene Biohazard Sample Bags, Catalog Number 01 826 5, supplied by Fisher Scientific, 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/pre-labeled and pre-weighed sample containers fisher scientific autoclavable polypropylene biohazard sample bags, catalog number 01-826-5/product/Fisher Scientific
Average 90 stars, based on 1 article reviews
pre-labeled and pre-weighed sample containers fisher scientific autoclavable polypropylene biohazard sample bags, catalog number 01-826-5 - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

90
Roboz Surgical fine forceps for tissue collection roboz surgical, catalog number: rs-5240
A. Injection pipettes made of glass capillaries are used for injection of cRNAs encoding for ion channels and other proteins in <t>Xenopus</t> oocytes. Injection workstation components labeled as follows: 1. Stereo microscope with external light source; 2. Micromanipulator and magnetic holding device; 3. Nanoinjector; 4. Nanoinjector controller. B. Loading of injection needle with cRNA. The injection needle is filled with mineral oil. A drop of the solution containing the cRNA of interest is place in the center of a piece of Parafilm. cRNA solution is collect with the injection pipette using the ‘fill’ bottom in the nanoinjector controller. C. Close view of oocytes aligned in a Petri dish. To prevent rolling during injection, oocytes are placed in a Petri dish with a polypropylene mesh glued to the bottom.
Fine Forceps For Tissue Collection Roboz Surgical, Catalog Number: Rs 5240, supplied by Roboz Surgical, 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/fine forceps for tissue collection roboz surgical, catalog number: rs-5240/product/Roboz Surgical
Average 90 stars, based on 1 article reviews
fine forceps for tissue collection roboz surgical, catalog number: rs-5240 - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

90
ApexBio molidustat (catalog number bay85-3934)
Some PHD inhibitors inhibit MBL oligomerization. (A) Representative Western blot showing the effects of PHD inhibitors (roxadustat [Rox], <t>molidustat</t> [Mol], and vadadustat [Vad], all at 10 µM) on expression of MBL, P4HA1, HIF1α, and α-tubulin. (B) Secreted MBL in light fraction (F1–F5) or heavy fraction (F6–F10) separated by sucrose gradient after 24-hour treatment with respective PHD inhibitors. (C) Quantification of the percentage of secreted MBL in the heavy fraction (compared to total MBL) in samples treated with different PHD inhibitors is shown. **P<0.01, ***P<0.001. (D) Representative distribution of relative proportion of secreted MBL (normalized to total secreted MBL) in ten fractions separated by sucrose density gradient for one sample from each group. Uncropped blots are provided in Supplemental Figure 6.
Molidustat (Catalog Number Bay85 3934), supplied by ApexBio, 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/molidustat (catalog number bay85-3934)/product/ApexBio
Average 90 stars, based on 1 article reviews
molidustat (catalog number bay85-3934) - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

90
Qiagen daglb (catalog number qt00173453)
Some PHD inhibitors inhibit MBL oligomerization. (A) Representative Western blot showing the effects of PHD inhibitors (roxadustat [Rox], <t>molidustat</t> [Mol], and vadadustat [Vad], all at 10 µM) on expression of MBL, P4HA1, HIF1α, and α-tubulin. (B) Secreted MBL in light fraction (F1–F5) or heavy fraction (F6–F10) separated by sucrose gradient after 24-hour treatment with respective PHD inhibitors. (C) Quantification of the percentage of secreted MBL in the heavy fraction (compared to total MBL) in samples treated with different PHD inhibitors is shown. **P<0.01, ***P<0.001. (D) Representative distribution of relative proportion of secreted MBL (normalized to total secreted MBL) in ten fractions separated by sucrose density gradient for one sample from each group. Uncropped blots are provided in Supplemental Figure 6.
Daglb (Catalog Number Qt00173453), supplied by Qiagen, 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/daglb (catalog number qt00173453)/product/Qiagen
Average 90 stars, based on 1 article reviews
daglb (catalog number qt00173453) - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

90
Qiagen cd4 antigen qt00096166
Primers purchased from Qiagen.
Cd4 Antigen Qt00096166, supplied by Qiagen, 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/cd4 antigen qt00096166/product/Qiagen
Average 90 stars, based on 1 article reviews
cd4 antigen qt00096166 - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

90
Fisher Bioreagents casamino acids fisher bioreagents catalog number bp1424-500
Primers purchased from Qiagen.
Casamino Acids Fisher Bioreagents Catalog Number Bp1424 500, supplied by Fisher Bioreagents, 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/casamino acids fisher bioreagents catalog number bp1424-500/product/Fisher Bioreagents
Average 90 stars, based on 1 article reviews
casamino acids fisher bioreagents catalog number bp1424-500 - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

90
Fisher Scientific acetonitrile (dna sequencing grade, catalog number bp-1170)
Primers purchased from Qiagen.
Acetonitrile (Dna Sequencing Grade, Catalog Number Bp 1170), supplied by Fisher Scientific, 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/acetonitrile (dna sequencing grade, catalog number bp-1170)/product/Fisher Scientific
Average 90 stars, based on 1 article reviews
acetonitrile (dna sequencing grade, catalog number bp-1170) - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

90
Becton Dickinson cell strainer catalog number 252350
Primers purchased from Qiagen.
Cell Strainer Catalog Number 252350, 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/result/cell strainer catalog number 252350/product/Becton Dickinson
Average 90 stars, based on 1 article reviews
cell strainer catalog number 252350 - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

Image Search Results


(A) Endogenous PDPK1 was recovered from lysates of the indicated cell lines and probed for co-precipitating WDR5 by IB. Inputs for PDPK1 are 10%–20%. Inputs for WDR5 are 1%–5%. n = 3 biological replicates. (B) Proximity ligation assay with FLAG and WDR5 antibodies in U2OS cells stably expressing FLAG-tagged PDPK1. Cells were treated overnight (30 μM C6/C6nc) before analysis; scale bar, 20 μm. n = 3 biological replicates. (C) HEK293 cells were treated overnight with 30 μM C6 or 5 μM GSK470, lysates prepared, and a PDPK1 IP performed. IB was then performed for the indicated proteins. Inputs are 5% for PDPK1 and 1% for all others. n = 3 biological replicates. (D) HEK293 cells were fractionated into cytosolic (S2), soluble nuclear (S3), and chromatin-associated (P3) fractions. Equal amounts of each fraction were analyzed by IB with the antibodies against the indicated proteins. H3 (nuclear) and α-tubulin (cytosolic) are controls for fractionation. n = 3 biological replicates. (E) Cytosolic and nuclear lysates from HEK293 cells were subject to IP with PDPK1 antibody or an IgG control and immunoblotted with antibodies against the indicated proteins. A short and long exposure of the WDR5 IB are shown. n = 3 biological replicates. (F) PDPK1 possesses two WIN-like motifs centered on R3 and R238. (G) FLAG-tagged PDPK1 (WT and the R3A and R238A mutants) were transiently expressed in HEK293 cells; lysates were prepared and subject to IP with anti-FLAG beads. Immune complexes were probed for PDPK1 or endogenous WDR5 by IB. n = 3 biological replicates. (H) FLAG-tagged PDPK1 (WT and the R3A) was transiently expressed in HEK293 cells, recovered by FLAG-IP, resolved by SDS-PAGE, and transferred to polyvinylidene fluoride (PVDF) membrane. Membranes were then incubated with recombinant WDR5 followed by anti-WDR5 antibody. n = 3 biological replicates. (I) In vitro -transcribed and -translated PDPK1-FLAG variants were incubated with recombinant 6xHis-SUMO-WDR5 proteins, recovered with Ni-NTA agarose, and analyzed by IB. n = 2 biological replicates. PH, pleckstrin homology domain. See also .

Journal: Cell reports

Article Title: Impact of WIN site inhibitor on the WDR5 interactome

doi: 10.1016/j.celrep.2020.108636

Figure Lengend Snippet: (A) Endogenous PDPK1 was recovered from lysates of the indicated cell lines and probed for co-precipitating WDR5 by IB. Inputs for PDPK1 are 10%–20%. Inputs for WDR5 are 1%–5%. n = 3 biological replicates. (B) Proximity ligation assay with FLAG and WDR5 antibodies in U2OS cells stably expressing FLAG-tagged PDPK1. Cells were treated overnight (30 μM C6/C6nc) before analysis; scale bar, 20 μm. n = 3 biological replicates. (C) HEK293 cells were treated overnight with 30 μM C6 or 5 μM GSK470, lysates prepared, and a PDPK1 IP performed. IB was then performed for the indicated proteins. Inputs are 5% for PDPK1 and 1% for all others. n = 3 biological replicates. (D) HEK293 cells were fractionated into cytosolic (S2), soluble nuclear (S3), and chromatin-associated (P3) fractions. Equal amounts of each fraction were analyzed by IB with the antibodies against the indicated proteins. H3 (nuclear) and α-tubulin (cytosolic) are controls for fractionation. n = 3 biological replicates. (E) Cytosolic and nuclear lysates from HEK293 cells were subject to IP with PDPK1 antibody or an IgG control and immunoblotted with antibodies against the indicated proteins. A short and long exposure of the WDR5 IB are shown. n = 3 biological replicates. (F) PDPK1 possesses two WIN-like motifs centered on R3 and R238. (G) FLAG-tagged PDPK1 (WT and the R3A and R238A mutants) were transiently expressed in HEK293 cells; lysates were prepared and subject to IP with anti-FLAG beads. Immune complexes were probed for PDPK1 or endogenous WDR5 by IB. n = 3 biological replicates. (H) FLAG-tagged PDPK1 (WT and the R3A) was transiently expressed in HEK293 cells, recovered by FLAG-IP, resolved by SDS-PAGE, and transferred to polyvinylidene fluoride (PVDF) membrane. Membranes were then incubated with recombinant WDR5 followed by anti-WDR5 antibody. n = 3 biological replicates. (I) In vitro -transcribed and -translated PDPK1-FLAG variants were incubated with recombinant 6xHis-SUMO-WDR5 proteins, recovered with Ni-NTA agarose, and analyzed by IB. n = 2 biological replicates. PH, pleckstrin homology domain. See also .

Article Snippet: PolyScreen PVDF Hybridization Transfer Membrane , PerkinElmer , Cat# NEF1002.

Techniques: Proximity Ligation Assay, Stable Transfection, Expressing, Fractionation, Control, SDS Page, Membrane, Incubation, Recombinant, In Vitro

A. Injection pipettes made of glass capillaries are used for injection of cRNAs encoding for ion channels and other proteins in Xenopus oocytes. Injection workstation components labeled as follows: 1. Stereo microscope with external light source; 2. Micromanipulator and magnetic holding device; 3. Nanoinjector; 4. Nanoinjector controller. B. Loading of injection needle with cRNA. The injection needle is filled with mineral oil. A drop of the solution containing the cRNA of interest is place in the center of a piece of Parafilm. cRNA solution is collect with the injection pipette using the ‘fill’ bottom in the nanoinjector controller. C. Close view of oocytes aligned in a Petri dish. To prevent rolling during injection, oocytes are placed in a Petri dish with a polypropylene mesh glued to the bottom.

Journal: Bio-protocol

Article Title: Expression and Analysis of Flow-regulated Ion Channels in Xenopus Oocytes

doi: 10.21769/BioProtoc.2224

Figure Lengend Snippet: A. Injection pipettes made of glass capillaries are used for injection of cRNAs encoding for ion channels and other proteins in Xenopus oocytes. Injection workstation components labeled as follows: 1. Stereo microscope with external light source; 2. Micromanipulator and magnetic holding device; 3. Nanoinjector; 4. Nanoinjector controller. B. Loading of injection needle with cRNA. The injection needle is filled with mineral oil. A drop of the solution containing the cRNA of interest is place in the center of a piece of Parafilm. cRNA solution is collect with the injection pipette using the ‘fill’ bottom in the nanoinjector controller. C. Close view of oocytes aligned in a Petri dish. To prevent rolling during injection, oocytes are placed in a Petri dish with a polypropylene mesh glued to the bottom.

Article Snippet: Harvesting of ovaries from female Xenopus laevis 2-L glass beaker Fine forceps for tissue collection (Roboz Surgical, catalog number: RS-5240) Fine scissors for tissue collection (Fine Science Tools, catalog number: 14060-09) Tissue forceps (Roboz Surgical, catalog number: RS-8162) B. Oocyte isolation and maintenance Dumont size 4 forceps (Fine Science Tools, catalog number: 11241-30) Clay Adams TM Nutator mixer (BD, catalog number: 421105) Oocytes transferring pipette: a polished glass Pasteur pipette (Fisher Scientific, Fisherbrand TM , catalog number: 13-678-20) Pipette pump (SP Scienceware - Bel-Art Products - H-B Instrument, catalog number: F378980000) B.O.D. low temperature refrigerated incubator (VWR) C. Oocyte injection Programmable nanoliter injector (Drummond Scientific, model: Nanoject III) Steel base plate (WPI, catalog number: 5052) Magnetic holding stand (WPI, catalog number: M10) Three-axis manual micromanipulator (WPI, catalog number: M3301) Stereo microscope (Olympus, model: SZ61) Fiber optic illuminator and bifurcated light guide (WPI) Micropipette pullers (NARISHIGE, model: PC10) D. Two-electrode voltage clamp Steel base plate (WPI, catalog number: 5479) Steel base plate (WPI, catalog number: 5052) Magnetic holding devices, three (WPI, catalog number: M10) Three-axis manual micromanipulators, three (WPI, catalog number: M3301) Two-electrode voltage clamp amplifier (Molecular Devices, Axon Accessories, model: GeneClamp 500B) Headstages (Molecular Devices, Axon Accessories, model: HS-2A) Virtual ground bath clamp (Molecular Devices, Axon Accessories, model: VG-2A) Pipette holders (Molecular Devices, model: HL-U) Ag/AgCl pellets (2 mm diameter, 4 mm long) (WPI, catalog number: EP2) Digitizer (Molecular Devices, model: Digidata 1550B) BNC cables (A-M systems) Perfusion system (Warner Instruments, model: VC-6) Flow valve (Warner Instruments, model: FR-50) Vacuum attached waste bottle (Fisher Scientific, Fisherbrand TM , catalog number: FB3002000) Oocyte chamber (20 mm diameter and 6 mm deep ring with glued glass bottom) Silver wire AWG 26 for electrodes (WPI, catalog number: AGW1510) PC computer with Windows operating system

Techniques: Injection, Labeling, Microscopy, Transferring

Some PHD inhibitors inhibit MBL oligomerization. (A) Representative Western blot showing the effects of PHD inhibitors (roxadustat [Rox], molidustat [Mol], and vadadustat [Vad], all at 10 µM) on expression of MBL, P4HA1, HIF1α, and α-tubulin. (B) Secreted MBL in light fraction (F1–F5) or heavy fraction (F6–F10) separated by sucrose gradient after 24-hour treatment with respective PHD inhibitors. (C) Quantification of the percentage of secreted MBL in the heavy fraction (compared to total MBL) in samples treated with different PHD inhibitors is shown. **P<0.01, ***P<0.001. (D) Representative distribution of relative proportion of secreted MBL (normalized to total secreted MBL) in ten fractions separated by sucrose density gradient for one sample from each group. Uncropped blots are provided in Supplemental Figure 6.

Journal: Kidney360

Article Title: Mannose Binding Lectin Is Hydroxylated by Collagen Prolyl-4-hydroxylase and Inhibited by Some PHD Inhibitors

doi: 10.34067/KID.0000092020

Figure Lengend Snippet: Some PHD inhibitors inhibit MBL oligomerization. (A) Representative Western blot showing the effects of PHD inhibitors (roxadustat [Rox], molidustat [Mol], and vadadustat [Vad], all at 10 µM) on expression of MBL, P4HA1, HIF1α, and α-tubulin. (B) Secreted MBL in light fraction (F1–F5) or heavy fraction (F6–F10) separated by sucrose gradient after 24-hour treatment with respective PHD inhibitors. (C) Quantification of the percentage of secreted MBL in the heavy fraction (compared to total MBL) in samples treated with different PHD inhibitors is shown. **P<0.01, ***P<0.001. (D) Representative distribution of relative proportion of secreted MBL (normalized to total secreted MBL) in ten fractions separated by sucrose density gradient for one sample from each group. Uncropped blots are provided in Supplemental Figure 6.

Article Snippet: Dimethyloxaloylglycine (DMOG; catalog number A4506) and molidustat (catalog number BAY85-3934) were purchased from ApexBio Technology.

Techniques: Western Blot, Expressing

Prolyl hydroxylation in the collagen-like region is significantly inhibited by roxadustat and vadadustat but not molidustat. Cells were treated with 10 µM of roxadustat, vadadustat, and molidustat for 24 hours. (A) Representative Western blots showing the effects of 24 hours of treatment with different PHD inhibitors on various proteins of interest in the lysates of MBL-expressing HEK293S cells. (B) Representative Western blots showing the effects of 24 hours of treatment with different PHD inhibitors on MBL secretion in the supernatant. The supernatant from three biologic replicates was concentrated and mass spectrometry analysis on the samples without knowledge of the treatments was undertaken. (C) Relative area of prolyl hydroxylated peptides covering the collagen-like domain containing hydroxylation at various proline residues (normalized to total area of MBL peptides within the collagen-like domain) in different conditions is shown. (D) Relative area of lysyl-modified (open circles) and unmodified (open squares) peptides covering the collagen-like domain (normalized by total area of MBL peptides within the collagen-like domain) in different conditions is shown. **P<0.01, ***P<0.001. Uncropped blots are provided in the Supplemental Figure 8.

Journal: Kidney360

Article Title: Mannose Binding Lectin Is Hydroxylated by Collagen Prolyl-4-hydroxylase and Inhibited by Some PHD Inhibitors

doi: 10.34067/KID.0000092020

Figure Lengend Snippet: Prolyl hydroxylation in the collagen-like region is significantly inhibited by roxadustat and vadadustat but not molidustat. Cells were treated with 10 µM of roxadustat, vadadustat, and molidustat for 24 hours. (A) Representative Western blots showing the effects of 24 hours of treatment with different PHD inhibitors on various proteins of interest in the lysates of MBL-expressing HEK293S cells. (B) Representative Western blots showing the effects of 24 hours of treatment with different PHD inhibitors on MBL secretion in the supernatant. The supernatant from three biologic replicates was concentrated and mass spectrometry analysis on the samples without knowledge of the treatments was undertaken. (C) Relative area of prolyl hydroxylated peptides covering the collagen-like domain containing hydroxylation at various proline residues (normalized to total area of MBL peptides within the collagen-like domain) in different conditions is shown. (D) Relative area of lysyl-modified (open circles) and unmodified (open squares) peptides covering the collagen-like domain (normalized by total area of MBL peptides within the collagen-like domain) in different conditions is shown. **P<0.01, ***P<0.001. Uncropped blots are provided in the Supplemental Figure 8.

Article Snippet: Dimethyloxaloylglycine (DMOG; catalog number A4506) and molidustat (catalog number BAY85-3934) were purchased from ApexBio Technology.

Techniques: Western Blot, Expressing, Mass Spectrometry, Modification

Primers purchased from Qiagen.

Journal: Molecular Medicine

Article Title: Cannabidiol Limits T Cell–Mediated Chronic Autoimmune Myocarditis: Implications to Autoimmune Disorders and Organ Transplantation

doi: 10.2119/molmed.2016.00007

Figure Lengend Snippet: Primers purchased from Qiagen.

Article Snippet: Data were normalized to the housekeeping gene β-actin. table ft1 table-wrap mode="anchored" t5 Table 1. caption a7 Gene Full name Qiagen reference Gene ID CD3e CD3 antigen, epsilon polypeptide QT01058764 {"type":"entrez-nucleotide","attrs":{"text":"NM_007648","term_id":"1402623766","term_text":"NM_007648"}} NM_007648 CD3g CD3 antigen, γ polypeptide QT00173481 {"type":"entrez-nucleotide","attrs":{"text":"NM_009850","term_id":"160333908","term_text":"NM_009850"}} NM_009850 CD4 CD4 antigen QT00096166 {"type":"entrez-nucleotide","attrs":{"text":"NM_013488.2","term_id":"133892562","term_text":"NM_013488.2"}} NM_013488.2 CD8a CD8 antigen, α chain QT00244433 {"type":"entrez-nucleotide","attrs":{"text":"NM_001081110","term_id":"126722839","term_text":"NM_001081110"}} NM_001081110 Itgax Integrin α X (CD11c) QT00113715 {"type":"entrez-nucleotide","attrs":{"text":"NM_021334","term_id":"1394533604","term_text":"NM_021334"}} NM_021334 EmR f4/80 Adgre1 adhesion G protein-coupled receptor E1 QT00099617 {"type":"entrez-nucleotide","attrs":{"text":"NM_010130","term_id":"183583543","term_text":"NM_010130"}} NM_010130 IL-6 Interleukin 6 QT00098875 {"type":"entrez-nucleotide","attrs":{"text":"NM_031168","term_id":"930945753","term_text":"NM_031168"}} NM_031168 IFN-γ Interferon γ QT01038821 {"type":"entrez-nucleotide","attrs":{"text":"NM_008337","term_id":"926657655","term_text":"NM_008337"}} NM_008337 Open in a separate window Gene ID and Qiagen reference number for CD3e, CD3g, CD4, CD8a, Itgax, EmR f4/80, IL-6 and IFN-γ are shown.

Techniques: