rabbit polyclonal p acc s79 Search Results


97
Cell Signaling Technology Inc rabbit polyclonal p acc s79
Key Resource Table
Rabbit Polyclonal P Acc S79, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/rabbit polyclonal p acc s79/product/Cell Signaling Technology Inc
Average 97 stars, based on 1 article reviews
rabbit polyclonal p acc s79 - by Bioz Stars, 2026-03
97/100 stars
  Buy from Supplier

96
Cell Signaling Technology Inc polyclonal p lkb1
Key Resource Table
Polyclonal P Lkb1, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/polyclonal p lkb1/product/Cell Signaling Technology Inc
Average 96 stars, based on 1 article reviews
polyclonal p lkb1 - by Bioz Stars, 2026-03
96/100 stars
  Buy from Supplier

96
Cell Signaling Technology Inc polyclonal p c raf
Key Resource Table
Polyclonal P C Raf, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/polyclonal p c raf/product/Cell Signaling Technology Inc
Average 96 stars, based on 1 article reviews
polyclonal p c raf - by Bioz Stars, 2026-03
96/100 stars
  Buy from Supplier

97
Cell Signaling Technology Inc polyclonal acc
Figure 1. Effects of LY3009120 on the adipogenesis and growth of differentiating 3T3‑L1 cells. (A) Protocol used to induce 3T3‑L1 preadipocyte differentia- tion. 3T3‑L1 preadipocytes were induced to differentiate with induction medium in the presence or absence of LY3009120 at the indicated concentrations and for the indicated times. (B) On D8, cellular lipid content was assessed by Oil Red O staining (upper panels). Phase‑contrast images of the cells were also recorded following treatment (lower panels). (C) On D8, cellular TG content was quantified using the AdipoRed assay. Values are presented as the mean ± stan- dard error of the mean of data from three independent experiments with three replicates. *P<0.05, vs. control. (D) On D8, LY3009120‑treated 3T3‑L1 cells, which are not stained by trypan blue dye, were counted under a microscope. The cell count assay was performed in triplicate. Data are presented as the mean ± standard error of the mean of data from three independent experiments. *P<0.05, vs. control. (E) 3T3‑L1 preadipocytes were induced to differentiate with induction medium in the presence or absence of LY3009120 at the indicated concentrations for 8 days. Cellular proteins were extracted and analyzed by western blot analysis. LY, LY3009120; MDI, IBMX, dexamethasone, and insulin; FBS, fetal bovine serum; D, day; TG, triglyceride; PARP, <t>polyclonal</t> poly (ADP‑ribose) polymerase; DR5, death receptor 5.
Polyclonal Acc, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/polyclonal acc/product/Cell Signaling Technology Inc
Average 97 stars, based on 1 article reviews
polyclonal acc - by Bioz Stars, 2026-03
97/100 stars
  Buy from Supplier

Image Search Results


Key Resource Table

Journal: Cell reports

Article Title: The transcription factors TFEB and TFE3 link the FLCN-AMPK signaling axis to innate immune response and pathogen resistance

doi: 10.1016/j.celrep.2019.02.102

Figure Lengend Snippet: Key Resource Table

Article Snippet: Rabbit polyclonal p-ACC (S79) , Cell Signaling , Cat#3661.

Techniques: Virus, Plasmid Preparation, shRNA, Clone Assay, Recombinant, Cell Viability Assay, Gene Expression, Microarray, Over Expression, Software

Figure 1. Effects of LY3009120 on the adipogenesis and growth of differentiating 3T3‑L1 cells. (A) Protocol used to induce 3T3‑L1 preadipocyte differentia- tion. 3T3‑L1 preadipocytes were induced to differentiate with induction medium in the presence or absence of LY3009120 at the indicated concentrations and for the indicated times. (B) On D8, cellular lipid content was assessed by Oil Red O staining (upper panels). Phase‑contrast images of the cells were also recorded following treatment (lower panels). (C) On D8, cellular TG content was quantified using the AdipoRed assay. Values are presented as the mean ± stan- dard error of the mean of data from three independent experiments with three replicates. *P<0.05, vs. control. (D) On D8, LY3009120‑treated 3T3‑L1 cells, which are not stained by trypan blue dye, were counted under a microscope. The cell count assay was performed in triplicate. Data are presented as the mean ± standard error of the mean of data from three independent experiments. *P<0.05, vs. control. (E) 3T3‑L1 preadipocytes were induced to differentiate with induction medium in the presence or absence of LY3009120 at the indicated concentrations for 8 days. Cellular proteins were extracted and analyzed by western blot analysis. LY, LY3009120; MDI, IBMX, dexamethasone, and insulin; FBS, fetal bovine serum; D, day; TG, triglyceride; PARP, polyclonal poly (ADP‑ribose) polymerase; DR5, death receptor 5.

Journal: International journal of molecular medicine

Article Title: LY3009120, a pan-Raf kinase inhibitor, inhibits adipogenesis of 3T3-L1 cells by controlling the expression and phosphorylation of C/EBP-α, PPAR-γ, STAT‑3, FAS, ACC, perilipin A, and AMPK.

doi: 10.3892/ijmm.2018.3890

Figure Lengend Snippet: Figure 1. Effects of LY3009120 on the adipogenesis and growth of differentiating 3T3‑L1 cells. (A) Protocol used to induce 3T3‑L1 preadipocyte differentia- tion. 3T3‑L1 preadipocytes were induced to differentiate with induction medium in the presence or absence of LY3009120 at the indicated concentrations and for the indicated times. (B) On D8, cellular lipid content was assessed by Oil Red O staining (upper panels). Phase‑contrast images of the cells were also recorded following treatment (lower panels). (C) On D8, cellular TG content was quantified using the AdipoRed assay. Values are presented as the mean ± stan- dard error of the mean of data from three independent experiments with three replicates. *P<0.05, vs. control. (D) On D8, LY3009120‑treated 3T3‑L1 cells, which are not stained by trypan blue dye, were counted under a microscope. The cell count assay was performed in triplicate. Data are presented as the mean ± standard error of the mean of data from three independent experiments. *P<0.05, vs. control. (E) 3T3‑L1 preadipocytes were induced to differentiate with induction medium in the presence or absence of LY3009120 at the indicated concentrations for 8 days. Cellular proteins were extracted and analyzed by western blot analysis. LY, LY3009120; MDI, IBMX, dexamethasone, and insulin; FBS, fetal bovine serum; D, day; TG, triglyceride; PARP, polyclonal poly (ADP‑ribose) polymerase; DR5, death receptor 5.

Article Snippet: Polyclonal p-AMPK (T172, cat. no. 2535), monoclonal AMPK (cat. no. 2793), polyclonal p-Acc (S79, cat. no. 3661), polyclonal Acc (cat. no. 3662), polyclonal liver kinase B1 (LKB1; cat. no. 3047), polyclonal p-LKB1 (S428, cat. no. 3482), polyclonal p-A-Raf (S299, cat. no. 4431), polyclonal A-Raf (cat. no. 4432), polyclonal p-B-Raf (S445, cat. no. 2696), polyclonal B-Raf (cat. no. 9433), polyclonal p-c-Raf (S259, cat. no. 9421), and monoclonal c-Raf (cat. no. 12552) antibodies were acquired from cell Signaling Technology, Inc. (danvers, MA, USA).

Techniques: Staining, Control, Microscopy, Cell Counting, Western Blot