acss1 Search Results


gene exp acss1 hs00287264 m1  (Thermo Fisher)
85
Thermo Fisher gene exp acss1 hs00287264 m1
Gene Exp Acss1 Hs00287264 M1, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/gene exp acss1 hs00287264 m1/product/Thermo Fisher
Average 85 stars, based on 1 article reviews
gene exp acss1 hs00287264 m1 - by Bioz Stars, 2026-03
85/100 stars
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myc tagged hspa8 plasmid pcmv3 acss1  (Sino Biological)
93
Sino Biological myc tagged hspa8 plasmid pcmv3 acss1
(A and B) HR LNCaP and C4-2 cells were treated with acetate (5 mM) for 24 h under hypoxia. (A) H3K9ac, H3K27ac, and H3 proteins were determined by western blot. H3 was the loading control. (B) BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. ACTB was the loading control. (C and D) Both <t>ACSS1</t> and ACSS2 were stably knocked down by shRNA in HR cells. (C) ACSS1, ACSS2, H3K9ac, H3K27ac, and H3 proteins were determined by Western blot. H3 was the loading control. (D) ACSS1, ACSS2, BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. (E and F) ACSS1 or ACSS2 was overexpressed in HR cells. (E) ACSS1, ACSS2, H3K9ac, H3K27ac, and H3 proteins were determined by western blot. H3 was the loading control. (F) BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. ACTB was the loading control. *p < 0.05 using a one sample two-tailed t test. Error bars represent mean ± SEM.
Myc Tagged Hspa8 Plasmid Pcmv3 Acss1, supplied by Sino Biological, 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/result/myc tagged hspa8 plasmid pcmv3 acss1/product/Sino Biological
Average 93 stars, based on 1 article reviews
myc tagged hspa8 plasmid pcmv3 acss1 - by Bioz Stars, 2026-03
93/100 stars
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acss1  (Proteintech)
93
Proteintech acss1
(A and B) HR LNCaP and C4-2 cells were treated with acetate (5 mM) for 24 h under hypoxia. (A) H3K9ac, H3K27ac, and H3 proteins were determined by western blot. H3 was the loading control. (B) BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. ACTB was the loading control. (C and D) Both <t>ACSS1</t> and ACSS2 were stably knocked down by shRNA in HR cells. (C) ACSS1, ACSS2, H3K9ac, H3K27ac, and H3 proteins were determined by Western blot. H3 was the loading control. (D) ACSS1, ACSS2, BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. (E and F) ACSS1 or ACSS2 was overexpressed in HR cells. (E) ACSS1, ACSS2, H3K9ac, H3K27ac, and H3 proteins were determined by western blot. H3 was the loading control. (F) BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. ACTB was the loading control. *p < 0.05 using a one sample two-tailed t test. Error bars represent mean ± SEM.
Acss1, supplied by Proteintech, 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/result/acss1/product/Proteintech
Average 93 stars, based on 1 article reviews
acss1 - by Bioz Stars, 2026-03
93/100 stars
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acss1  (Atlas Antibodies)
94
Atlas Antibodies acss1
(A and B) HR LNCaP and C4-2 cells were treated with acetate (5 mM) for 24 h under hypoxia. (A) H3K9ac, H3K27ac, and H3 proteins were determined by western blot. H3 was the loading control. (B) BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. ACTB was the loading control. (C and D) Both <t>ACSS1</t> and ACSS2 were stably knocked down by shRNA in HR cells. (C) ACSS1, ACSS2, H3K9ac, H3K27ac, and H3 proteins were determined by Western blot. H3 was the loading control. (D) ACSS1, ACSS2, BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. (E and F) ACSS1 or ACSS2 was overexpressed in HR cells. (E) ACSS1, ACSS2, H3K9ac, H3K27ac, and H3 proteins were determined by western blot. H3 was the loading control. (F) BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. ACTB was the loading control. *p < 0.05 using a one sample two-tailed t test. Error bars represent mean ± SEM.
Acss1, supplied by Atlas Antibodies, 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/result/acss1/product/Atlas Antibodies
Average 94 stars, based on 1 article reviews
acss1 - by Bioz Stars, 2026-03
94/100 stars
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sc 373847  (Santa Cruz Biotechnology)
91
Santa Cruz Biotechnology sc 373847
(A and B) HR LNCaP and C4-2 cells were treated with acetate (5 mM) for 24 h under hypoxia. (A) H3K9ac, H3K27ac, and H3 proteins were determined by western blot. H3 was the loading control. (B) BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. ACTB was the loading control. (C and D) Both <t>ACSS1</t> and ACSS2 were stably knocked down by shRNA in HR cells. (C) ACSS1, ACSS2, H3K9ac, H3K27ac, and H3 proteins were determined by Western blot. H3 was the loading control. (D) ACSS1, ACSS2, BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. (E and F) ACSS1 or ACSS2 was overexpressed in HR cells. (E) ACSS1, ACSS2, H3K9ac, H3K27ac, and H3 proteins were determined by western blot. H3 was the loading control. (F) BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. ACTB was the loading control. *p < 0.05 using a one sample two-tailed t test. Error bars represent mean ± SEM.
Sc 373847, supplied by Santa Cruz Biotechnology, 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/sc 373847/product/Santa Cruz Biotechnology
Average 91 stars, based on 1 article reviews
sc 373847 - by Bioz Stars, 2026-03
91/100 stars
  Buy from Supplier
gene exp acss1 mm00475647 m1  (Thermo Fisher)
85
Thermo Fisher gene exp acss1 mm00475647 m1
(A and B) HR LNCaP and C4-2 cells were treated with acetate (5 mM) for 24 h under hypoxia. (A) H3K9ac, H3K27ac, and H3 proteins were determined by western blot. H3 was the loading control. (B) BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. ACTB was the loading control. (C and D) Both <t>ACSS1</t> and ACSS2 were stably knocked down by shRNA in HR cells. (C) ACSS1, ACSS2, H3K9ac, H3K27ac, and H3 proteins were determined by Western blot. H3 was the loading control. (D) ACSS1, ACSS2, BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. (E and F) ACSS1 or ACSS2 was overexpressed in HR cells. (E) ACSS1, ACSS2, H3K9ac, H3K27ac, and H3 proteins were determined by western blot. H3 was the loading control. (F) BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. ACTB was the loading control. *p < 0.05 using a one sample two-tailed t test. Error bars represent mean ± SEM.
Gene Exp Acss1 Mm00475647 M1, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/gene exp acss1 mm00475647 m1/product/Thermo Fisher
Average 85 stars, based on 1 article reviews
gene exp acss1 mm00475647 m1 - by Bioz Stars, 2026-03
85/100 stars
  Buy from Supplier
gene exp acss1 hs00544656 g1  (Thermo Fisher)
91
Thermo Fisher gene exp acss1 hs00544656 g1
(A and B) HR LNCaP and C4-2 cells were treated with acetate (5 mM) for 24 h under hypoxia. (A) H3K9ac, H3K27ac, and H3 proteins were determined by western blot. H3 was the loading control. (B) BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. ACTB was the loading control. (C and D) Both <t>ACSS1</t> and ACSS2 were stably knocked down by shRNA in HR cells. (C) ACSS1, ACSS2, H3K9ac, H3K27ac, and H3 proteins were determined by Western blot. H3 was the loading control. (D) ACSS1, ACSS2, BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. (E and F) ACSS1 or ACSS2 was overexpressed in HR cells. (E) ACSS1, ACSS2, H3K9ac, H3K27ac, and H3 proteins were determined by western blot. H3 was the loading control. (F) BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. ACTB was the loading control. *p < 0.05 using a one sample two-tailed t test. Error bars represent mean ± SEM.
Gene Exp Acss1 Hs00544656 G1, supplied by Thermo Fisher, 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/gene exp acss1 hs00544656 g1/product/Thermo Fisher
Average 91 stars, based on 1 article reviews
gene exp acss1 hs00544656 g1 - by Bioz Stars, 2026-03
91/100 stars
  Buy from Supplier
acss1 a15007 antibody  (ABclonal Biotechnology)
90
ABclonal Biotechnology acss1 a15007 antibody
(A and B) HR LNCaP and C4-2 cells were treated with acetate (5 mM) for 24 h under hypoxia. (A) H3K9ac, H3K27ac, and H3 proteins were determined by western blot. H3 was the loading control. (B) BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. ACTB was the loading control. (C and D) Both <t>ACSS1</t> and ACSS2 were stably knocked down by shRNA in HR cells. (C) ACSS1, ACSS2, H3K9ac, H3K27ac, and H3 proteins were determined by Western blot. H3 was the loading control. (D) ACSS1, ACSS2, BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. (E and F) ACSS1 or ACSS2 was overexpressed in HR cells. (E) ACSS1, ACSS2, H3K9ac, H3K27ac, and H3 proteins were determined by western blot. H3 was the loading control. (F) BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. ACTB was the loading control. *p < 0.05 using a one sample two-tailed t test. Error bars represent mean ± SEM.
Acss1 A15007 Antibody, supplied by ABclonal 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/result/acss1 a15007 antibody/product/ABclonal Biotechnology
Average 90 stars, based on 1 article reviews
acss1 a15007 antibody - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier
human acss1 gene orf cdna clone expression plasmid  (Sino Biological)
93
Sino Biological human acss1 gene orf cdna clone expression plasmid
(A and B) HR LNCaP and C4-2 cells were treated with acetate (5 mM) for 24 h under hypoxia. (A) H3K9ac, H3K27ac, and H3 proteins were determined by western blot. H3 was the loading control. (B) BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. ACTB was the loading control. (C and D) Both <t>ACSS1</t> and ACSS2 were stably knocked down by shRNA in HR cells. (C) ACSS1, ACSS2, H3K9ac, H3K27ac, and H3 proteins were determined by Western blot. H3 was the loading control. (D) ACSS1, ACSS2, BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. (E and F) ACSS1 or ACSS2 was overexpressed in HR cells. (E) ACSS1, ACSS2, H3K9ac, H3K27ac, and H3 proteins were determined by western blot. H3 was the loading control. (F) BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. ACTB was the loading control. *p < 0.05 using a one sample two-tailed t test. Error bars represent mean ± SEM.
Human Acss1 Gene Orf Cdna Clone Expression Plasmid, supplied by Sino Biological, 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/result/human acss1 gene orf cdna clone expression plasmid/product/Sino Biological
Average 93 stars, based on 1 article reviews
human acss1 gene orf cdna clone expression plasmid - by Bioz Stars, 2026-03
93/100 stars
  Buy from Supplier
acetyl acss1  (Cusabio)
91
Cusabio acetyl acss1
(A and B) HR LNCaP and C4-2 cells were treated with acetate (5 mM) for 24 h under hypoxia. (A) H3K9ac, H3K27ac, and H3 proteins were determined by western blot. H3 was the loading control. (B) BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. ACTB was the loading control. (C and D) Both <t>ACSS1</t> and ACSS2 were stably knocked down by shRNA in HR cells. (C) ACSS1, ACSS2, H3K9ac, H3K27ac, and H3 proteins were determined by Western blot. H3 was the loading control. (D) ACSS1, ACSS2, BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. (E and F) ACSS1 or ACSS2 was overexpressed in HR cells. (E) ACSS1, ACSS2, H3K9ac, H3K27ac, and H3 proteins were determined by western blot. H3 was the loading control. (F) BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. ACTB was the loading control. *p < 0.05 using a one sample two-tailed t test. Error bars represent mean ± SEM.
Acetyl Acss1, supplied by Cusabio, 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/acetyl acss1/product/Cusabio
Average 91 stars, based on 1 article reviews
acetyl acss1 - by Bioz Stars, 2026-03
91/100 stars
  Buy from Supplier
acss1 antibody  (Bio-Techne corporation)
90
Bio-Techne corporation acss1 antibody
(A and B) HR LNCaP and C4-2 cells were treated with acetate (5 mM) for 24 h under hypoxia. (A) H3K9ac, H3K27ac, and H3 proteins were determined by western blot. H3 was the loading control. (B) BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. ACTB was the loading control. (C and D) Both <t>ACSS1</t> and ACSS2 were stably knocked down by shRNA in HR cells. (C) ACSS1, ACSS2, H3K9ac, H3K27ac, and H3 proteins were determined by Western blot. H3 was the loading control. (D) ACSS1, ACSS2, BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. (E and F) ACSS1 or ACSS2 was overexpressed in HR cells. (E) ACSS1, ACSS2, H3K9ac, H3K27ac, and H3 proteins were determined by western blot. H3 was the loading control. (F) BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. ACTB was the loading control. *p < 0.05 using a one sample two-tailed t test. Error bars represent mean ± SEM.
Acss1 Antibody, supplied by Bio-Techne corporation, 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/acss1 antibody/product/Bio-Techne corporation
Average 90 stars, based on 1 article reviews
acss1 antibody - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier

Image Search Results


(A and B) HR LNCaP and C4-2 cells were treated with acetate (5 mM) for 24 h under hypoxia. (A) H3K9ac, H3K27ac, and H3 proteins were determined by western blot. H3 was the loading control. (B) BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. ACTB was the loading control. (C and D) Both ACSS1 and ACSS2 were stably knocked down by shRNA in HR cells. (C) ACSS1, ACSS2, H3K9ac, H3K27ac, and H3 proteins were determined by Western blot. H3 was the loading control. (D) ACSS1, ACSS2, BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. (E and F) ACSS1 or ACSS2 was overexpressed in HR cells. (E) ACSS1, ACSS2, H3K9ac, H3K27ac, and H3 proteins were determined by western blot. H3 was the loading control. (F) BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. ACTB was the loading control. *p < 0.05 using a one sample two-tailed t test. Error bars represent mean ± SEM.

Journal: Cell reports

Article Title: Chronic hypoxia stabilizes 3βHSD1 via autophagy suppression

doi: 10.1016/j.celrep.2023.113575

Figure Lengend Snippet: (A and B) HR LNCaP and C4-2 cells were treated with acetate (5 mM) for 24 h under hypoxia. (A) H3K9ac, H3K27ac, and H3 proteins were determined by western blot. H3 was the loading control. (B) BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. ACTB was the loading control. (C and D) Both ACSS1 and ACSS2 were stably knocked down by shRNA in HR cells. (C) ACSS1, ACSS2, H3K9ac, H3K27ac, and H3 proteins were determined by Western blot. H3 was the loading control. (D) ACSS1, ACSS2, BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. (E and F) ACSS1 or ACSS2 was overexpressed in HR cells. (E) ACSS1, ACSS2, H3K9ac, H3K27ac, and H3 proteins were determined by western blot. H3 was the loading control. (F) BECN1, ATG10, ATG7, ATG3, ATG4A, ATG4B, LC3B , and ATG2A mRNA was determined by qPCR. ACTB was the loading control. *p < 0.05 using a one sample two-tailed t test. Error bars represent mean ± SEM.

Article Snippet: The following plasmids were purchased from Sino Biological: plasmid pCMV3-OFPSpark-LC3A (HG14322-ANR) expressing N-terminal OFPSpark-tagged LC3A plasmid pCMV3-HSD3B1-HA (HG14410-CY) expressing C-terminal HA tagged HSD3B1 plasmid pCMV3-HSPA8-Myc (HG11329-CM) expressing C-terminal Myc tagged HSPA8 plasmid pCMV3-ACSS1 (HG12250-UT) expressing ACSS1 plasmid pCMV3-ACSS2-HA (HG22964-CY) expressing C-terminal HA tagged ACSS2 .

Techniques: Western Blot, Stable Transfection, shRNA, Two Tailed Test

KEY RESOURCES TABLE

Journal: Cell reports

Article Title: Chronic hypoxia stabilizes 3βHSD1 via autophagy suppression

doi: 10.1016/j.celrep.2023.113575

Figure Lengend Snippet: KEY RESOURCES TABLE

Article Snippet: The following plasmids were purchased from Sino Biological: plasmid pCMV3-OFPSpark-LC3A (HG14322-ANR) expressing N-terminal OFPSpark-tagged LC3A plasmid pCMV3-HSD3B1-HA (HG14410-CY) expressing C-terminal HA tagged HSD3B1 plasmid pCMV3-HSPA8-Myc (HG11329-CM) expressing C-terminal Myc tagged HSPA8 plasmid pCMV3-ACSS1 (HG12250-UT) expressing ACSS1 plasmid pCMV3-ACSS2-HA (HG22964-CY) expressing C-terminal HA tagged ACSS2 .

Techniques: Recombinant, Transfection, Mutagenesis, Viability Assay, Sequencing, Negative Control, shRNA, Plasmid Preparation, Expressing, Variant Assay, Software