short chain fatty acids Search Results


93
Proteintech anti elovl6
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OriGene anti elovl3 antibodies
Anti Elovl3 Antibodies, supplied by OriGene, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Rockland Immunochemicals 600 401 ep0
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Boster Bio acsl4 antibody
Primers used in this study.
Acsl4 Antibody, 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
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Boster Bio primary antibody rabbit acsl1 polyclonal antibody
Primers used in this study.
Primary Antibody Rabbit Acsl1 Polyclonal Antibody, supplied by Boster Bio, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Boster Bio slc27a5
The expression and function of <t>SLC27A5</t> in HCC. ( A – C ) The transcriptional expression of SLC27A5 in HCC and normal tissues of TCGA-LIHC ( A ), GSE14520 ( B ) and GSE64041 ( C ) datasets. ( D ) The protein level of SLC27A5 in HCC and normal tissues. ( E , F ) CCK-8 assay for HepG2 ( E ) and LM-3 ( F ) cells overexpressing SL27A5. ( G , H ) HepG2 ( G ) and LM-3 ( H ) cells were subject to flow cytometry analysis for cell cycle. ( I ) HCC cells overexpressing SLC27A5 were subject to EdU staining. ( J ) HCC cells overexpressing SLC27A5 were subject to wound healing assay.
Slc27a5, 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
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Boster Bio elovl1
The expression and function of <t>SLC27A5</t> in HCC. ( A – C ) The transcriptional expression of SLC27A5 in HCC and normal tissues of TCGA-LIHC ( A ), GSE14520 ( B ) and GSE64041 ( C ) datasets. ( D ) The protein level of SLC27A5 in HCC and normal tissues. ( E , F ) CCK-8 assay for HepG2 ( E ) and LM-3 ( F ) cells overexpressing SL27A5. ( G , H ) HepG2 ( G ) and LM-3 ( H ) cells were subject to flow cytometry analysis for cell cycle. ( I ) HCC cells overexpressing SLC27A5 were subject to EdU staining. ( J ) HCC cells overexpressing SLC27A5 were subject to wound healing assay.
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OriGene elongation
The expression and function of <t>SLC27A5</t> in HCC. ( A – C ) The transcriptional expression of SLC27A5 in HCC and normal tissues of TCGA-LIHC ( A ), GSE14520 ( B ) and GSE64041 ( C ) datasets. ( D ) The protein level of SLC27A5 in HCC and normal tissues. ( E , F ) CCK-8 assay for HepG2 ( E ) and LM-3 ( F ) cells overexpressing SL27A5. ( G , H ) HepG2 ( G ) and LM-3 ( H ) cells were subject to flow cytometry analysis for cell cycle. ( I ) HCC cells overexpressing SLC27A5 were subject to EdU staining. ( J ) HCC cells overexpressing SLC27A5 were subject to wound healing assay.
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Boster Bio slc27a2
The expression and function of <t>SLC27A5</t> in HCC. ( A – C ) The transcriptional expression of SLC27A5 in HCC and normal tissues of TCGA-LIHC ( A ), GSE14520 ( B ) and GSE64041 ( C ) datasets. ( D ) The protein level of SLC27A5 in HCC and normal tissues. ( E , F ) CCK-8 assay for HepG2 ( E ) and LM-3 ( F ) cells overexpressing SL27A5. ( G , H ) HepG2 ( G ) and LM-3 ( H ) cells were subject to flow cytometry analysis for cell cycle. ( I ) HCC cells overexpressing SLC27A5 were subject to EdU staining. ( J ) HCC cells overexpressing SLC27A5 were subject to wound healing assay.
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MicroLumen inc surface treated with any long chain fatty acid
The expression and function of <t>SLC27A5</t> in HCC. ( A – C ) The transcriptional expression of SLC27A5 in HCC and normal tissues of TCGA-LIHC ( A ), GSE14520 ( B ) and GSE64041 ( C ) datasets. ( D ) The protein level of SLC27A5 in HCC and normal tissues. ( E , F ) CCK-8 assay for HepG2 ( E ) and LM-3 ( F ) cells overexpressing SL27A5. ( G , H ) HepG2 ( G ) and LM-3 ( H ) cells were subject to flow cytometry analysis for cell cycle. ( I ) HCC cells overexpressing SLC27A5 were subject to EdU staining. ( J ) HCC cells overexpressing SLC27A5 were subject to wound healing assay.
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Ordway Research Institute Inc exogenous long chain fatty acids (lcfas)
The expression and function of <t>SLC27A5</t> in HCC. ( A – C ) The transcriptional expression of SLC27A5 in HCC and normal tissues of TCGA-LIHC ( A ), GSE14520 ( B ) and GSE64041 ( C ) datasets. ( D ) The protein level of SLC27A5 in HCC and normal tissues. ( E , F ) CCK-8 assay for HepG2 ( E ) and LM-3 ( F ) cells overexpressing SL27A5. ( G , H ) HepG2 ( G ) and LM-3 ( H ) cells were subject to flow cytometry analysis for cell cycle. ( I ) HCC cells overexpressing SLC27A5 were subject to EdU staining. ( J ) HCC cells overexpressing SLC27A5 were subject to wound healing assay.
Exogenous Long Chain Fatty Acids (Lcfas), supplied by Ordway Research Institute Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Primers used in this study.

Journal: Frontiers in Oncology

Article Title: Scutellaria barbata Inhibits Hepatocellular Carcinoma Tumorigenicity by Inducing Ferroptosis of Hepatocellular Carcinoma Cells

doi: 10.3389/fonc.2022.693395

Figure Lengend Snippet: Primers used in this study.

Article Snippet: The primary antibodies used in the present study were diluted into 5% nonfat milk as follow: GPX4 antibody (PAC994Hu01, USCN, Wuhan, China, 1:1,000), ACSL4 antibody (A04372-2, Boster, Wuhan, China, 1:1,000), CCRB1 (SLC7A11) antibody (bs-6883R, Bioss, Beijing, China, 1:1,000), IREB2 antibody (PAH789Hu01, USCN, 1:1,000), and GAPDH antibody (KC-5G5, Aksomics, Shanghai, China, 1:10,000).

Techniques: Sequencing

Scutellaria barbata induces ferroptosis through regulating genes involved in lipid ROS metabolism and iron perioxidation in HCC cells. (A) The mRNA levels of GPX4, SLC7A11, IREB2, and ACSL4 were detected by RT-PCR in HCC cell lines (SMMC-7721, HepG2, and Huh7) with or without S. barbata treatment. (B) The protein levels of GPX4, SLC7A11, IREB2, and ACSL4 were detected by Western blot analysis in HCC cell lines (SMMC-7721, HepG2, and Huh7) with or without S. barbata treatment. Data were representative of three independent experiments and analyzed by unpaired t-test. Error bars denote SD. *p < 0.05.

Journal: Frontiers in Oncology

Article Title: Scutellaria barbata Inhibits Hepatocellular Carcinoma Tumorigenicity by Inducing Ferroptosis of Hepatocellular Carcinoma Cells

doi: 10.3389/fonc.2022.693395

Figure Lengend Snippet: Scutellaria barbata induces ferroptosis through regulating genes involved in lipid ROS metabolism and iron perioxidation in HCC cells. (A) The mRNA levels of GPX4, SLC7A11, IREB2, and ACSL4 were detected by RT-PCR in HCC cell lines (SMMC-7721, HepG2, and Huh7) with or without S. barbata treatment. (B) The protein levels of GPX4, SLC7A11, IREB2, and ACSL4 were detected by Western blot analysis in HCC cell lines (SMMC-7721, HepG2, and Huh7) with or without S. barbata treatment. Data were representative of three independent experiments and analyzed by unpaired t-test. Error bars denote SD. *p < 0.05.

Article Snippet: The primary antibodies used in the present study were diluted into 5% nonfat milk as follow: GPX4 antibody (PAC994Hu01, USCN, Wuhan, China, 1:1,000), ACSL4 antibody (A04372-2, Boster, Wuhan, China, 1:1,000), CCRB1 (SLC7A11) antibody (bs-6883R, Bioss, Beijing, China, 1:1,000), IREB2 antibody (PAH789Hu01, USCN, 1:1,000), and GAPDH antibody (KC-5G5, Aksomics, Shanghai, China, 1:10,000).

Techniques: Reverse Transcription Polymerase Chain Reaction, Western Blot

The expression and function of SLC27A5 in HCC. ( A – C ) The transcriptional expression of SLC27A5 in HCC and normal tissues of TCGA-LIHC ( A ), GSE14520 ( B ) and GSE64041 ( C ) datasets. ( D ) The protein level of SLC27A5 in HCC and normal tissues. ( E , F ) CCK-8 assay for HepG2 ( E ) and LM-3 ( F ) cells overexpressing SL27A5. ( G , H ) HepG2 ( G ) and LM-3 ( H ) cells were subject to flow cytometry analysis for cell cycle. ( I ) HCC cells overexpressing SLC27A5 were subject to EdU staining. ( J ) HCC cells overexpressing SLC27A5 were subject to wound healing assay.

Journal: Aging (Albany NY)

Article Title: Copper metabolism-related risk score identifies hepatocellular carcinoma subtypes and SLC27A5 as a potential regulator of cuproptosis

doi: 10.18632/aging.205334

Figure Lengend Snippet: The expression and function of SLC27A5 in HCC. ( A – C ) The transcriptional expression of SLC27A5 in HCC and normal tissues of TCGA-LIHC ( A ), GSE14520 ( B ) and GSE64041 ( C ) datasets. ( D ) The protein level of SLC27A5 in HCC and normal tissues. ( E , F ) CCK-8 assay for HepG2 ( E ) and LM-3 ( F ) cells overexpressing SL27A5. ( G , H ) HepG2 ( G ) and LM-3 ( H ) cells were subject to flow cytometry analysis for cell cycle. ( I ) HCC cells overexpressing SLC27A5 were subject to EdU staining. ( J ) HCC cells overexpressing SLC27A5 were subject to wound healing assay.

Article Snippet: Western blotting was performed using antibodies against FDX1 (M05441, Boster), SLC27A5 (A09287-2, Boster), GAPDH (BM3876, Boster).

Techniques: Expressing, CCK-8 Assay, Flow Cytometry, Staining, Wound Healing Assay

SLC27A5 upregulates FDX1 in HCC. ( A , B ) The correlation between the expression of SLC27A5 and that of FDX1 in TCGA-LIHC ( A ) and GSE14520 ( B ) datasets. ( C ) Dot plot showing the dependency scores for SLC27A5 and FDX1 across all tumor cell lines in the Project Achilles/Cancer Dependency Map Portal (DepMap). ( D , E ) The expression of and correlation between SLC27A5 and FDX1 in collected HCC tissue chip. ( F , G ) HepG2 ( F ) and LM-3 ( G ) cells overexpressing SLC27A5 were subject to qRT-PCR analysis. ( H , I ) Western blotting using lysates of HepG2 ( H ) and LM-3 ( I ) cells after overexpressing SLC27A5.

Journal: Aging (Albany NY)

Article Title: Copper metabolism-related risk score identifies hepatocellular carcinoma subtypes and SLC27A5 as a potential regulator of cuproptosis

doi: 10.18632/aging.205334

Figure Lengend Snippet: SLC27A5 upregulates FDX1 in HCC. ( A , B ) The correlation between the expression of SLC27A5 and that of FDX1 in TCGA-LIHC ( A ) and GSE14520 ( B ) datasets. ( C ) Dot plot showing the dependency scores for SLC27A5 and FDX1 across all tumor cell lines in the Project Achilles/Cancer Dependency Map Portal (DepMap). ( D , E ) The expression of and correlation between SLC27A5 and FDX1 in collected HCC tissue chip. ( F , G ) HepG2 ( F ) and LM-3 ( G ) cells overexpressing SLC27A5 were subject to qRT-PCR analysis. ( H , I ) Western blotting using lysates of HepG2 ( H ) and LM-3 ( I ) cells after overexpressing SLC27A5.

Article Snippet: Western blotting was performed using antibodies against FDX1 (M05441, Boster), SLC27A5 (A09287-2, Boster), GAPDH (BM3876, Boster).

Techniques: Expressing, Quantitative RT-PCR, Western Blot