acss2 Search Results


89
Thermo Fisher gene exp acss2 mm00480101 m1
Gene Exp Acss2 Mm00480101 M1, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 89/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 89 stars, based on 1 article reviews
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93
Sino Biological ha tagged acss2
(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 <t>ACSS2</t> 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.
Ha Tagged Acss2, 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
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Average 93 stars, based on 1 article reviews
ha tagged acss2 - by Bioz Stars, 2026-02
93/100 stars
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93
Thermo Fisher gene exp acss2 rn01753668 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 ACSS1 and <t>ACSS2</t> 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 Acss2 Rn01753668 M1, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 93 stars, based on 1 article reviews
gene exp acss2 rn01753668 m1 - by Bioz Stars, 2026-02
93/100 stars
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94
Selleck Chemicals acss2 inhibitor vy 3 249
(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 <t>ACSS2</t> 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.
Acss2 Inhibitor Vy 3 249, supplied by Selleck Chemicals, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 94 stars, based on 1 article reviews
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93
Proteintech 1 ap
(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 <t>ACSS2</t> 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.
1 Ap, 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
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Average 93 stars, based on 1 article reviews
1 ap - by Bioz Stars, 2026-02
93/100 stars
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86
Thermo Fisher gene exp plin1 hs01106925 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 ACSS1 and <t>ACSS2</t> 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 Plin1 Hs01106925 M1, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 86 stars, based on 1 article reviews
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86/100 stars
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93
Santa Cruz Biotechnology acss2
(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 <t>ACSS2</t> 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.
Acss2, supplied by Santa Cruz Biotechnology, 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/acss2/product/Santa Cruz Biotechnology
Average 93 stars, based on 1 article reviews
acss2 - by Bioz Stars, 2026-02
93/100 stars
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88
Thermo Fisher gene exp acss2 hs00218766 m1
Gene Expression Changes in Primary Sebocytes After 48 hrs
Gene Exp Acss2 Hs00218766 M1, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 88/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 88 stars, based on 1 article reviews
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93
MedChemExpress acss2 inhibitor
Gene Expression Changes in Primary Sebocytes After 48 hrs
Acss2 Inhibitor, supplied by MedChemExpress, 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/acss2 inhibitor/product/MedChemExpress
Average 93 stars, based on 1 article reviews
acss2 inhibitor - by Bioz Stars, 2026-02
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91
Thermo Fisher gene exp acss2 hs01122829 m1
Gene Expression Changes in Primary Sebocytes After 48 hrs
Gene Exp Acss2 Hs01122829 M1, 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
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Average 91 stars, based on 1 article reviews
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93
MedChemExpress acss2
Gene Expression Changes in Primary Sebocytes After 48 hrs
Acss2, supplied by MedChemExpress, 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/acss2/product/MedChemExpress
Average 93 stars, based on 1 article reviews
acss2 - by Bioz Stars, 2026-02
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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

Gene Expression Changes in Primary Sebocytes After 48 hrs

Journal: Clinical, Cosmetic and Investigational Dermatology

Article Title: Biguanides Induce Acute de novo Lipogenesis in Human Primary Sebocytes

doi: 10.2147/CCID.S243154

Figure Lengend Snippet: Gene Expression Changes in Primary Sebocytes After 48 hrs

Article Snippet: Reverse transcription reactions were prepared using 1 μg of total RNA and qPCR analysis was performed in duplicate using 10 ng/well cDNA to determine the transcript levels of SREBF1 (Hs01088691_m1), FASN (Hs01005622_m1), ACSS2 (Hs00218766_m1), SCD (Hs01682761_m1), HMGCR (Hs00168352_m1), SQLE (Hs01123768_m1), ACLY (Hs00982738_m1), ACACA (Hs1046047_m1), ELOVL6 (Hs00907564_m1), KRT7 (Hs00559840_m1), MUC1 (Hs00159357_m1) and TBP (Hs00427620_m1) Taqman probes (Life Technologies, Waltham, MA).

Techniques: Gene Expression