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Axon Medchem LLC bx430
Bx430, supplied by Axon Medchem LLC, 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/bx430/bx430/10__1021_slash_acsptsci__4c00688-173-0-4
Average 90 stars, based on 1 article reviews
bx430 - by Bioz Stars, 2026-09
90/100 stars

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Article Title: Species Differences of P2X4 Receptor Modulators
Article Snippet: The P2X4 receptor is an ATP-gated ion channel that was proposed as a novel drug target for neuropathic pain, neurodegenerative diseases, epilepsy, and cancer.. Animal models are indispensable for elucidating the role of receptors in health and disease and for drug development.. Here, we present a systematic analysis and comparison of P2X4 receptors of nine different species that are relevant for basic and applied research, human, monkey, dog, guinea pig, pig, rabbit, rat, mouse, and zebrafish.



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Tocris bx430
(A-B) Number of Ca2+ spikes in MA104-GCaMP cells in RV-infected (SA11cl3-mRuby3) at MOI 0.01 and neighboring (NB)+3 cell, treated with: (A) DMSO, 30μM 18β-glycyrrhetinic acid (18β-gly), or 50μM TAT-Gap19 (Gap19) and imaged ~8–24 hpi or (B) anti-VP7 M60 MAb, anti-NSP4 MAb 622, or rabbit anti-NSP4 antisera 120–147 (Rb Ab) and imaged ~8–24 hpi. (data combined from N=3 independent experiments) (C) Representative images of intercellular calcium waves in MA104-GCaMP cells infected with RV (SA11cl3-mRuby3) at MOI 0.1 and mock- or 10U/mL apyrase-treated (5 U/mL apyrase VI and 5U/mL apyrase VII) and imaged ~10 hpi with (D) representative Ca2+ traces from ~8–25 hpi. (E) Ca2+ spikes in RV-infected and NB cells. (F) Average magnitude of Ca2+ spikes/cell in RV-infected and NB cells, (data combined from N=3 independent experiments). (G) qPCR of purinergic receptor mRNA normalized to 18S mRNA and fold change relative to P2X3 mRNA transcript levels in MA104 cells, (data combined from N=3 independent experiments) (H-I) Ca2+ spikes in MA104-GCaMP cells RV (SA114F)-infected (H) or neighboring (NB) cells (I) and treated with DMSO, 10μM BPTU, 10μM AR-C 118925XX (ARC), 10μM <t>Bx430,</t> or 10μM 5-BDBD (data combined from N=3 independent experiments). (A-B, E-F, H-I) Kruskal-Wallis with Dunn’s multiple comparisons test used. Scale bar = 100 μm. Data represented as mean ± SD, (*p<0.05, ****p<0.0001).
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(A-B) Number of Ca2+ spikes in MA104-GCaMP cells in RV-infected (SA11cl3-mRuby3) at MOI 0.01 and neighboring (NB)+3 cell, treated with: (A) DMSO, 30μM 18β-glycyrrhetinic acid (18β-gly), or 50μM TAT-Gap19 (Gap19) and imaged ~8–24 hpi or (B) anti-VP7 M60 MAb, anti-NSP4 MAb 622, or rabbit anti-NSP4 antisera 120–147 (Rb Ab) and imaged ~8–24 hpi. (data combined from N=3 independent experiments) (C) Representative images of intercellular calcium waves in MA104-GCaMP cells infected with RV (SA11cl3-mRuby3) at MOI 0.1 and mock- or 10U/mL apyrase-treated (5 U/mL apyrase VI and 5U/mL apyrase VII) and imaged ~10 hpi with (D) representative Ca2+ traces from ~8–25 hpi. (E) Ca2+ spikes in RV-infected and NB cells. (F) Average magnitude of Ca2+ spikes/cell in RV-infected and NB cells, (data combined from N=3 independent experiments). (G) qPCR of purinergic receptor mRNA normalized to 18S mRNA and fold change relative to P2X3 mRNA transcript levels in MA104 cells, (data combined from N=3 independent experiments) (H-I) Ca2+ spikes in MA104-GCaMP cells RV (SA114F)-infected (H) or neighboring (NB) cells (I) and treated with DMSO, 10μM BPTU, 10μM AR-C 118925XX (ARC), 10μM Bx430, or 10μM 5-BDBD (data combined from N=3 independent experiments). (A-B, E-F, H-I) Kruskal-Wallis with Dunn’s multiple comparisons test used. Scale bar = 100 μm. Data represented as mean ± SD, (*p<0.05, ****p<0.0001).

Journal: Science (New York, N.Y.)

Article Title: Rotavirus induces intercellular calcium waves through ADP signaling

doi: 10.1126/science.abc3621

Figure Lengend Snippet: (A-B) Number of Ca2+ spikes in MA104-GCaMP cells in RV-infected (SA11cl3-mRuby3) at MOI 0.01 and neighboring (NB)+3 cell, treated with: (A) DMSO, 30μM 18β-glycyrrhetinic acid (18β-gly), or 50μM TAT-Gap19 (Gap19) and imaged ~8–24 hpi or (B) anti-VP7 M60 MAb, anti-NSP4 MAb 622, or rabbit anti-NSP4 antisera 120–147 (Rb Ab) and imaged ~8–24 hpi. (data combined from N=3 independent experiments) (C) Representative images of intercellular calcium waves in MA104-GCaMP cells infected with RV (SA11cl3-mRuby3) at MOI 0.1 and mock- or 10U/mL apyrase-treated (5 U/mL apyrase VI and 5U/mL apyrase VII) and imaged ~10 hpi with (D) representative Ca2+ traces from ~8–25 hpi. (E) Ca2+ spikes in RV-infected and NB cells. (F) Average magnitude of Ca2+ spikes/cell in RV-infected and NB cells, (data combined from N=3 independent experiments). (G) qPCR of purinergic receptor mRNA normalized to 18S mRNA and fold change relative to P2X3 mRNA transcript levels in MA104 cells, (data combined from N=3 independent experiments) (H-I) Ca2+ spikes in MA104-GCaMP cells RV (SA114F)-infected (H) or neighboring (NB) cells (I) and treated with DMSO, 10μM BPTU, 10μM AR-C 118925XX (ARC), 10μM Bx430, or 10μM 5-BDBD (data combined from N=3 independent experiments). (A-B, E-F, H-I) Kruskal-Wallis with Dunn’s multiple comparisons test used. Scale bar = 100 μm. Data represented as mean ± SD, (*p<0.05, ****p<0.0001).

Article Snippet: BPTU, AR-C 118925XX, Bx430, 5-BDBD, MRS2179, MRS2279, MRS2500, 10-Panx, suramin, TAT-Gap19, PPADS (Pyridoxalphosphate-6-azophenyl-2’,4’-disulfonic acid), NOC-7, prostaglandin E2, ARL 67156, and ω-agatoxin were purchased from Tocris Bioscience.

Techniques: Infection

(A) J3 jHIE-GCaMP6s monolayers mock- or RV (Ito)-infected produce intercellular calcium waves originating at a cell (arrowheads), imaged at ~4 hpi. (B) IF images of (J3)HIE-GCaMP6s monolayers mock- or RV-infected, fixed at 24 hpi, and immunostained for RV antigen (pink) and counterstained with DAPI (gray). (C) Ca2+ spikes per field-of-view (FOV), in (J3)HIEs mock- or RV-infected and treated with vehicle, 100 μM carbenoxolone (CBX), or 10 μM 10Panx at 8–22 hpi (data combined from N=3 independent experiments). (D) qPCR of purinergic receptor mRNA normalized to 18S mRNA and fold change relative to P2X3 mRNA transcript levels in (J3)HIE monolayers (data combined from N=3 independent experiments). (E) Representative Ca2+ traces/FOV of (J3)HIE-GCaMP6s monolayers either mock- or RV-infected and treated with DMSO, 100 U/mL apyrase, or 10 μM BPTU between 8.5–22 hpi. Mock- or RV-infected (J3)HIEs, treated with DMSO, apyrase, or purinergic receptor blockers. (F) Ca2+ spikes/FOV in (J3)HIE-GCaMP6s monolayers treated with DMSO, 100U/mL apyrase (50 U/mL apyrase VI and 50U/mL apyrase VII), 10 μM BPTU, 10 μM AR-C 118925XX, 10 μM Bx430, or 10 μM 5-BDBD and (G) average magnitude of Ca2+ spikes/FOV for 8.5–22 hpi, (data combined from N=3 independent experiments) (H) Ca2+ spikes/FOV of patient J2 jHIE-GCaMP6s monolayers mock- or RV-infected and treated with DMSO, 10 μM BPTU, 10 μM MRS2179, 10 μM MRS2279, or 10 μM MRS2500 and (I) average magnitude of Ca2+ spikes/FOV for 8–22 hpi, (data combined from N=3 independent experiments). (C,H,I) One-way ANOVA with Bonferroni’s and (F,G) Kruskal-Wallis with Dunn’s multiple corrections test used. Scale bar = 50 μm. Data represented as mean ± SD, (*p<0.05, **p<0.01, ***p<0.001, ****p<0.0001)

Journal: Science (New York, N.Y.)

Article Title: Rotavirus induces intercellular calcium waves through ADP signaling

doi: 10.1126/science.abc3621

Figure Lengend Snippet: (A) J3 jHIE-GCaMP6s monolayers mock- or RV (Ito)-infected produce intercellular calcium waves originating at a cell (arrowheads), imaged at ~4 hpi. (B) IF images of (J3)HIE-GCaMP6s monolayers mock- or RV-infected, fixed at 24 hpi, and immunostained for RV antigen (pink) and counterstained with DAPI (gray). (C) Ca2+ spikes per field-of-view (FOV), in (J3)HIEs mock- or RV-infected and treated with vehicle, 100 μM carbenoxolone (CBX), or 10 μM 10Panx at 8–22 hpi (data combined from N=3 independent experiments). (D) qPCR of purinergic receptor mRNA normalized to 18S mRNA and fold change relative to P2X3 mRNA transcript levels in (J3)HIE monolayers (data combined from N=3 independent experiments). (E) Representative Ca2+ traces/FOV of (J3)HIE-GCaMP6s monolayers either mock- or RV-infected and treated with DMSO, 100 U/mL apyrase, or 10 μM BPTU between 8.5–22 hpi. Mock- or RV-infected (J3)HIEs, treated with DMSO, apyrase, or purinergic receptor blockers. (F) Ca2+ spikes/FOV in (J3)HIE-GCaMP6s monolayers treated with DMSO, 100U/mL apyrase (50 U/mL apyrase VI and 50U/mL apyrase VII), 10 μM BPTU, 10 μM AR-C 118925XX, 10 μM Bx430, or 10 μM 5-BDBD and (G) average magnitude of Ca2+ spikes/FOV for 8.5–22 hpi, (data combined from N=3 independent experiments) (H) Ca2+ spikes/FOV of patient J2 jHIE-GCaMP6s monolayers mock- or RV-infected and treated with DMSO, 10 μM BPTU, 10 μM MRS2179, 10 μM MRS2279, or 10 μM MRS2500 and (I) average magnitude of Ca2+ spikes/FOV for 8–22 hpi, (data combined from N=3 independent experiments). (C,H,I) One-way ANOVA with Bonferroni’s and (F,G) Kruskal-Wallis with Dunn’s multiple corrections test used. Scale bar = 50 μm. Data represented as mean ± SD, (*p<0.05, **p<0.01, ***p<0.001, ****p<0.0001)

Article Snippet: BPTU, AR-C 118925XX, Bx430, 5-BDBD, MRS2179, MRS2279, MRS2500, 10-Panx, suramin, TAT-Gap19, PPADS (Pyridoxalphosphate-6-azophenyl-2’,4’-disulfonic acid), NOC-7, prostaglandin E2, ARL 67156, and ω-agatoxin were purchased from Tocris Bioscience.

Techniques: Infection

(A) Rotavirus yield from SA114F-infected MA104 cells treated with DMSO vehicle, 10U/mL apyrase, 10μM BPTU, 10μM AR-C 118925XX, 20μM Bx430, 20μM 5-BDBD, 300μM suramin, or 10μM PPADS by fluorescent focus assay (data combined from N=3 independent experiments). (B) Plaque assay yield of RV (SA114F)-infected MA104-GCaMP (Par) or MA104-GCaMP P2Y1 knockout (KO) cells (data combined from N=3 independent experiments). (C-E) qPCR of mRNA transcripts normalized to 18S mRNA transcripts and fold change relative to the Mock-DMSO transcript levels in (J3)HIE monolayers mock- or RV (Ito)-infected and treated with DMSO vehicle, 100U/mL apyrase, or 10 μM BPTU (data combined from N=3 independent experiments). (F-G) Serotonin secretion from RV (Ito)-infected jHIE (F) monolayers and (G) transwells treated with DMSO, 100U/mL apyrase, 10μM BPTU, or 300nM ω-agatoxin (data combined from N=3 independent experiments). (H) Enteroid swelling assay: 3D jHIE-GCaMP6s enteroids mock- or RV (Ito)-infected and treated with DMSO or 10μM BPTU. Cross-sectional area of the internal lumen (pink outline) used for percent increase between basal and max swelling (left panels). Scale bar = 100μm. (n ≥ 68 HIEs per condition, data combined from N=3 independent experiments) (I-K) C57Bl/6J mouse pups with diarrhea infected with Rhesus RV and vehicle- or BPTU-treated and the (J) mean diarrhea score. (data combined from 4 cages of each condition, 26–30 pups total per condition, mean ± SEM) (K) Summary model of RV-induced ICWs mediated by extracellular ADP. (A-B, F-G) One-way ANOVA with Bonferroni multiple comparisons test, (C-J) Kruskal-Wallis with Dunn’s multiple comparisons, or (I-J) Mann-Whitney tests used. (A-H) Data represented as mean ± SD, (*p<0.05, **p<0.01, ***p<0.001, ****p<0.0001).

Journal: Science (New York, N.Y.)

Article Title: Rotavirus induces intercellular calcium waves through ADP signaling

doi: 10.1126/science.abc3621

Figure Lengend Snippet: (A) Rotavirus yield from SA114F-infected MA104 cells treated with DMSO vehicle, 10U/mL apyrase, 10μM BPTU, 10μM AR-C 118925XX, 20μM Bx430, 20μM 5-BDBD, 300μM suramin, or 10μM PPADS by fluorescent focus assay (data combined from N=3 independent experiments). (B) Plaque assay yield of RV (SA114F)-infected MA104-GCaMP (Par) or MA104-GCaMP P2Y1 knockout (KO) cells (data combined from N=3 independent experiments). (C-E) qPCR of mRNA transcripts normalized to 18S mRNA transcripts and fold change relative to the Mock-DMSO transcript levels in (J3)HIE monolayers mock- or RV (Ito)-infected and treated with DMSO vehicle, 100U/mL apyrase, or 10 μM BPTU (data combined from N=3 independent experiments). (F-G) Serotonin secretion from RV (Ito)-infected jHIE (F) monolayers and (G) transwells treated with DMSO, 100U/mL apyrase, 10μM BPTU, or 300nM ω-agatoxin (data combined from N=3 independent experiments). (H) Enteroid swelling assay: 3D jHIE-GCaMP6s enteroids mock- or RV (Ito)-infected and treated with DMSO or 10μM BPTU. Cross-sectional area of the internal lumen (pink outline) used for percent increase between basal and max swelling (left panels). Scale bar = 100μm. (n ≥ 68 HIEs per condition, data combined from N=3 independent experiments) (I-K) C57Bl/6J mouse pups with diarrhea infected with Rhesus RV and vehicle- or BPTU-treated and the (J) mean diarrhea score. (data combined from 4 cages of each condition, 26–30 pups total per condition, mean ± SEM) (K) Summary model of RV-induced ICWs mediated by extracellular ADP. (A-B, F-G) One-way ANOVA with Bonferroni multiple comparisons test, (C-J) Kruskal-Wallis with Dunn’s multiple comparisons, or (I-J) Mann-Whitney tests used. (A-H) Data represented as mean ± SD, (*p<0.05, **p<0.01, ***p<0.001, ****p<0.0001).

Article Snippet: BPTU, AR-C 118925XX, Bx430, 5-BDBD, MRS2179, MRS2279, MRS2500, 10-Panx, suramin, TAT-Gap19, PPADS (Pyridoxalphosphate-6-azophenyl-2’,4’-disulfonic acid), NOC-7, prostaglandin E2, ARL 67156, and ω-agatoxin were purchased from Tocris Bioscience.

Techniques: Infection, Plaque Assay, Knock-Out, MANN-WHITNEY