kinase 1 ask1 Search Results


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ELISA for estimation of Human Apoptosis signal regulating Kinase 1, ASK-1 in serum, plasma and other biological fluids
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93
Boster Bio anti ask1
Anti Ask1, supplied by Boster Bio, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/kinase+1+ask1/Anti-ASK+1+MAP3K5+Antibody/pm35179864__ac1c05181_si_001-10-7-30
Average 93 stars, based on 1 article reviews
anti ask1 - by Bioz Stars, 2026-10
93/100 stars
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90
ProSci Incorporated ask1
AS-IV attenuated ER stress and ER stress-induced apoptotic pathway in the kidney of db/db mice. (A,B) Representative pictures for GRP78 immunohistochemistry staining (A) and quantification of IOD (B) for GRP78 in each group. Scale bars, 10 μm; Original magnification, ×400. (C,D) Western blot analyses (C) and densitometric quantification (D) of GRP78 expression in the kidney cortex lysates from each group. (E,F) Representative immunoblots (E) and densitometric quantification (F) of ATF6, p-PERK, p-eIF2α, ATF4, CHOP expression in total lysates of kidney cortex from each group. (G,H) Representative immunoblots (G) and densitometric quantification (H) of p-IRE1α, spliced-XBP1, TRAF2, <t>ASK1,</t> and phospho-JNK Thr183/Tyr185 expression in total lysates of kidney cortex from each group. (I,J) Representative immunoblots (I) and densitometric quantification (J) of cleaved caspase 12, cleaved caspase 9 and cleaved caspase 3 expression in total lysates of kidney cortex from each group. Data are expressed as mean ± SEM. n = 6. ∗∗ P < 0.01; # P < 0.05 and ## P < 0.01. One-way ANOVA and Newman–Keuls multiple comparisons test (B,D,F,H,J) .
Ask1, supplied by ProSci Incorporated, 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/kinase+1+ask1/ASK1+Antibody/pmc05174081-71-98-100
Average 90 stars, based on 1 article reviews
ask1 - by Bioz Stars, 2026-10
90/100 stars
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90
Signal Research apoptosis signal-research regulating kinase1 (ask1)
AS-IV attenuated ER stress and ER stress-induced apoptotic pathway in the kidney of db/db mice. (A,B) Representative pictures for GRP78 immunohistochemistry staining (A) and quantification of IOD (B) for GRP78 in each group. Scale bars, 10 μm; Original magnification, ×400. (C,D) Western blot analyses (C) and densitometric quantification (D) of GRP78 expression in the kidney cortex lysates from each group. (E,F) Representative immunoblots (E) and densitometric quantification (F) of ATF6, p-PERK, p-eIF2α, ATF4, CHOP expression in total lysates of kidney cortex from each group. (G,H) Representative immunoblots (G) and densitometric quantification (H) of p-IRE1α, spliced-XBP1, TRAF2, <t>ASK1,</t> and phospho-JNK Thr183/Tyr185 expression in total lysates of kidney cortex from each group. (I,J) Representative immunoblots (I) and densitometric quantification (J) of cleaved caspase 12, cleaved caspase 9 and cleaved caspase 3 expression in total lysates of kidney cortex from each group. Data are expressed as mean ± SEM. n = 6. ∗∗ P < 0.01; # P < 0.05 and ## P < 0.01. One-way ANOVA and Newman–Keuls multiple comparisons test (B,D,F,H,J) .
Apoptosis Signal Research Regulating Kinase1 (Ask1), supplied by Signal Research, 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/kinase+1+ask1/apoptosis+signal+research+regulating+kinase1++ask1+/pmc05823020-287-15-16
Average 90 stars, based on 1 article reviews
apoptosis signal-research regulating kinase1 (ask1) - by Bioz Stars, 2026-10
90/100 stars
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94
MedChemExpress phospho ask1 ser966
AS-IV attenuated ER stress and ER stress-induced apoptotic pathway in the kidney of db/db mice. (A,B) Representative pictures for GRP78 immunohistochemistry staining (A) and quantification of IOD (B) for GRP78 in each group. Scale bars, 10 μm; Original magnification, ×400. (C,D) Western blot analyses (C) and densitometric quantification (D) of GRP78 expression in the kidney cortex lysates from each group. (E,F) Representative immunoblots (E) and densitometric quantification (F) of ATF6, p-PERK, p-eIF2α, ATF4, CHOP expression in total lysates of kidney cortex from each group. (G,H) Representative immunoblots (G) and densitometric quantification (H) of p-IRE1α, spliced-XBP1, TRAF2, <t>ASK1,</t> and phospho-JNK Thr183/Tyr185 expression in total lysates of kidney cortex from each group. (I,J) Representative immunoblots (I) and densitometric quantification (J) of cleaved caspase 12, cleaved caspase 9 and cleaved caspase 3 expression in total lysates of kidney cortex from each group. Data are expressed as mean ± SEM. n = 6. ∗∗ P < 0.01; # P < 0.05 and ## P < 0.01. One-way ANOVA and Newman–Keuls multiple comparisons test (B,D,F,H,J) .
Phospho Ask1 Ser966, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/kinase+1+ask1/Phospho-ASK1+(Ser966)+Antibody/pm41621573-58-0-8
Average 94 stars, based on 1 article reviews
phospho ask1 ser966 - by Bioz Stars, 2026-10
94/100 stars
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94
MedChemExpress ask1
AS-IV attenuated ER stress and ER stress-induced apoptotic pathway in the kidney of db/db mice. (A,B) Representative pictures for GRP78 immunohistochemistry staining (A) and quantification of IOD (B) for GRP78 in each group. Scale bars, 10 μm; Original magnification, ×400. (C,D) Western blot analyses (C) and densitometric quantification (D) of GRP78 expression in the kidney cortex lysates from each group. (E,F) Representative immunoblots (E) and densitometric quantification (F) of ATF6, p-PERK, p-eIF2α, ATF4, CHOP expression in total lysates of kidney cortex from each group. (G,H) Representative immunoblots (G) and densitometric quantification (H) of p-IRE1α, spliced-XBP1, TRAF2, <t>ASK1,</t> and phospho-JNK Thr183/Tyr185 expression in total lysates of kidney cortex from each group. (I,J) Representative immunoblots (I) and densitometric quantification (J) of cleaved caspase 12, cleaved caspase 9 and cleaved caspase 3 expression in total lysates of kidney cortex from each group. Data are expressed as mean ± SEM. n = 6. ∗∗ P < 0.01; # P < 0.05 and ## P < 0.01. One-way ANOVA and Newman–Keuls multiple comparisons test (B,D,F,H,J) .
Ask1, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/kinase+1+ask1/ASK1%2C+Human/pm41519004-19-29-51
Average 94 stars, based on 1 article reviews
ask1 - by Bioz Stars, 2026-10
94/100 stars
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90
Makoto USA Inc apoptosis signal-regulating kinase 1 (ask1)
AS-IV attenuated ER stress and ER stress-induced apoptotic pathway in the kidney of db/db mice. (A,B) Representative pictures for GRP78 immunohistochemistry staining (A) and quantification of IOD (B) for GRP78 in each group. Scale bars, 10 μm; Original magnification, ×400. (C,D) Western blot analyses (C) and densitometric quantification (D) of GRP78 expression in the kidney cortex lysates from each group. (E,F) Representative immunoblots (E) and densitometric quantification (F) of ATF6, p-PERK, p-eIF2α, ATF4, CHOP expression in total lysates of kidney cortex from each group. (G,H) Representative immunoblots (G) and densitometric quantification (H) of p-IRE1α, spliced-XBP1, TRAF2, <t>ASK1,</t> and phospho-JNK Thr183/Tyr185 expression in total lysates of kidney cortex from each group. (I,J) Representative immunoblots (I) and densitometric quantification (J) of cleaved caspase 12, cleaved caspase 9 and cleaved caspase 3 expression in total lysates of kidney cortex from each group. Data are expressed as mean ± SEM. n = 6. ∗∗ P < 0.01; # P < 0.05 and ## P < 0.01. One-way ANOVA and Newman–Keuls multiple comparisons test (B,D,F,H,J) .
Apoptosis Signal Regulating Kinase 1 (Ask1), supplied by Makoto USA 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/product/kinase+1+ask1/apoptosis+signal+regulating+kinase+1++ask1+/pm20006657-10-181-39
Average 90 stars, based on 1 article reviews
apoptosis signal-regulating kinase 1 (ask1) - by Bioz Stars, 2026-10
90/100 stars
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90
MyBiosource Biotechnology apoptosis signal regulating kinase (ask)-1
AS-IV attenuated ER stress and ER stress-induced apoptotic pathway in the kidney of db/db mice. (A,B) Representative pictures for GRP78 immunohistochemistry staining (A) and quantification of IOD (B) for GRP78 in each group. Scale bars, 10 μm; Original magnification, ×400. (C,D) Western blot analyses (C) and densitometric quantification (D) of GRP78 expression in the kidney cortex lysates from each group. (E,F) Representative immunoblots (E) and densitometric quantification (F) of ATF6, p-PERK, p-eIF2α, ATF4, CHOP expression in total lysates of kidney cortex from each group. (G,H) Representative immunoblots (G) and densitometric quantification (H) of p-IRE1α, spliced-XBP1, TRAF2, <t>ASK1,</t> and phospho-JNK Thr183/Tyr185 expression in total lysates of kidney cortex from each group. (I,J) Representative immunoblots (I) and densitometric quantification (J) of cleaved caspase 12, cleaved caspase 9 and cleaved caspase 3 expression in total lysates of kidney cortex from each group. Data are expressed as mean ± SEM. n = 6. ∗∗ P < 0.01; # P < 0.05 and ## P < 0.01. One-way ANOVA and Newman–Keuls multiple comparisons test (B,D,F,H,J) .
Apoptosis Signal Regulating Kinase (Ask) 1, supplied by MyBiosource Biotechnology, 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/kinase+1+ask1/apoptosis+signal+regulating+kinase+1++ask1++kit/pm34564023-68-36-38
Average 90 stars, based on 1 article reviews
apoptosis signal regulating kinase (ask)-1 - by Bioz Stars, 2026-10
90/100 stars
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Polyclonal Antibody to Apoptosis Signal Regulating Kinase 1 ASK1
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Image Search Results


AS-IV attenuated ER stress and ER stress-induced apoptotic pathway in the kidney of db/db mice. (A,B) Representative pictures for GRP78 immunohistochemistry staining (A) and quantification of IOD (B) for GRP78 in each group. Scale bars, 10 μm; Original magnification, ×400. (C,D) Western blot analyses (C) and densitometric quantification (D) of GRP78 expression in the kidney cortex lysates from each group. (E,F) Representative immunoblots (E) and densitometric quantification (F) of ATF6, p-PERK, p-eIF2α, ATF4, CHOP expression in total lysates of kidney cortex from each group. (G,H) Representative immunoblots (G) and densitometric quantification (H) of p-IRE1α, spliced-XBP1, TRAF2, ASK1, and phospho-JNK Thr183/Tyr185 expression in total lysates of kidney cortex from each group. (I,J) Representative immunoblots (I) and densitometric quantification (J) of cleaved caspase 12, cleaved caspase 9 and cleaved caspase 3 expression in total lysates of kidney cortex from each group. Data are expressed as mean ± SEM. n = 6. ∗∗ P < 0.01; # P < 0.05 and ## P < 0.01. One-way ANOVA and Newman–Keuls multiple comparisons test (B,D,F,H,J) .

Journal: Frontiers in Pharmacology

Article Title: Astragaloside IV Attenuates Podocyte Apoptosis Mediated by Endoplasmic Reticulum Stress through Upregulating Sarco/Endoplasmic Reticulum Ca 2+ -ATPase 2 Expression in Diabetic Nephropathy

doi: 10.3389/fphar.2016.00500

Figure Lengend Snippet: AS-IV attenuated ER stress and ER stress-induced apoptotic pathway in the kidney of db/db mice. (A,B) Representative pictures for GRP78 immunohistochemistry staining (A) and quantification of IOD (B) for GRP78 in each group. Scale bars, 10 μm; Original magnification, ×400. (C,D) Western blot analyses (C) and densitometric quantification (D) of GRP78 expression in the kidney cortex lysates from each group. (E,F) Representative immunoblots (E) and densitometric quantification (F) of ATF6, p-PERK, p-eIF2α, ATF4, CHOP expression in total lysates of kidney cortex from each group. (G,H) Representative immunoblots (G) and densitometric quantification (H) of p-IRE1α, spliced-XBP1, TRAF2, ASK1, and phospho-JNK Thr183/Tyr185 expression in total lysates of kidney cortex from each group. (I,J) Representative immunoblots (I) and densitometric quantification (J) of cleaved caspase 12, cleaved caspase 9 and cleaved caspase 3 expression in total lysates of kidney cortex from each group. Data are expressed as mean ± SEM. n = 6. ∗∗ P < 0.01; # P < 0.05 and ## P < 0.01. One-way ANOVA and Newman–Keuls multiple comparisons test (B,D,F,H,J) .

Article Snippet: The following primary antibodies were used: eIF2α, JNK, phospho-JNK Thr183/Tyr185 , AIF, cyclophilin D, and ANT from Santa Cruz Biotechnology (Santa Cruz, CA, USA), GAPDH, SERCA1, inositol-requiring enzyme 1α (IRE1α), TNF receptor associated factor 2 (TRAF2), PERK, phospho-PERK Thr980 , phospho-eIF2α Ser51 , activating transcription factor 4 (ATF4), caspase 12, caspase 9, caspase 3, CHOP, and cytochrome c from Cell Signaling Technology (Danvers, MA, USA), SERCA2, Podocin, Nephrin, GRP78, ATF6, XBP1, voltage dependent anion channel 1 (VDAC1), APAF1, and PPARγ from Abcam company (Cambridge, MA, USA), phospho-IRE1α Ser724 from Novus Biologicals, SERCA3 from Proteintech Group (Chicago, IL, USA), ASK1 from ProSci Incorporated (San Diego, CA, USA).

Techniques: Immunohistochemistry, Staining, Western Blot, Expressing

AS-IV restored SERCA2 expression and inhibited ER stress-mediated apoptosis in palmitate-stimulated podocytes. Podocytes were pretreated with or without AS-IV at the indicated concentrations (20, 40, and 80 μM respectively) for 12 h followed by 250 μM palmitate exposure for 24h. (A) Representative flow cytometry results for podocytes under different cultural conditions. (B) Semiquantitative data showing percentage of apoptotic podocytes under different cultural conditions. (C,D) Representative immunoblots (C) and quantification (D) of Podocin, SERCA2 and GRP78 under different conditions. (E) SERCA activity under different conditions. (F,G) Representative immunoblots (F) and quantification (G) of key molecules in ATF6-CHOP/PERK–eIF-2α–ATF4–CHOP signaling pathways under different conditions. (H,I) Representative immunoblots (H) and quantification (I) of key molecules in IRE1–XBP1/IRE1-TRAF2–ASK1–JNK signaling pathway. (J,K) Representative immunoblots (J) and quantification (K) of cleaved caspase 12 and cleaved caspase 3 under different conditions. Data are expressed as mean ± SEM. n = 3–5. ∗∗ P < 0.01; # P < 0.05 and ## P < 0.01. One-way ANOVA and Newman–Keuls multiple comparisons test (B,D,E,G,I,K) .

Journal: Frontiers in Pharmacology

Article Title: Astragaloside IV Attenuates Podocyte Apoptosis Mediated by Endoplasmic Reticulum Stress through Upregulating Sarco/Endoplasmic Reticulum Ca 2+ -ATPase 2 Expression in Diabetic Nephropathy

doi: 10.3389/fphar.2016.00500

Figure Lengend Snippet: AS-IV restored SERCA2 expression and inhibited ER stress-mediated apoptosis in palmitate-stimulated podocytes. Podocytes were pretreated with or without AS-IV at the indicated concentrations (20, 40, and 80 μM respectively) for 12 h followed by 250 μM palmitate exposure for 24h. (A) Representative flow cytometry results for podocytes under different cultural conditions. (B) Semiquantitative data showing percentage of apoptotic podocytes under different cultural conditions. (C,D) Representative immunoblots (C) and quantification (D) of Podocin, SERCA2 and GRP78 under different conditions. (E) SERCA activity under different conditions. (F,G) Representative immunoblots (F) and quantification (G) of key molecules in ATF6-CHOP/PERK–eIF-2α–ATF4–CHOP signaling pathways under different conditions. (H,I) Representative immunoblots (H) and quantification (I) of key molecules in IRE1–XBP1/IRE1-TRAF2–ASK1–JNK signaling pathway. (J,K) Representative immunoblots (J) and quantification (K) of cleaved caspase 12 and cleaved caspase 3 under different conditions. Data are expressed as mean ± SEM. n = 3–5. ∗∗ P < 0.01; # P < 0.05 and ## P < 0.01. One-way ANOVA and Newman–Keuls multiple comparisons test (B,D,E,G,I,K) .

Article Snippet: The following primary antibodies were used: eIF2α, JNK, phospho-JNK Thr183/Tyr185 , AIF, cyclophilin D, and ANT from Santa Cruz Biotechnology (Santa Cruz, CA, USA), GAPDH, SERCA1, inositol-requiring enzyme 1α (IRE1α), TNF receptor associated factor 2 (TRAF2), PERK, phospho-PERK Thr980 , phospho-eIF2α Ser51 , activating transcription factor 4 (ATF4), caspase 12, caspase 9, caspase 3, CHOP, and cytochrome c from Cell Signaling Technology (Danvers, MA, USA), SERCA2, Podocin, Nephrin, GRP78, ATF6, XBP1, voltage dependent anion channel 1 (VDAC1), APAF1, and PPARγ from Abcam company (Cambridge, MA, USA), phospho-IRE1α Ser724 from Novus Biologicals, SERCA3 from Proteintech Group (Chicago, IL, USA), ASK1 from ProSci Incorporated (San Diego, CA, USA).

Techniques: Expressing, Flow Cytometry, Western Blot, Activity Assay, Protein-Protein interactions