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slc25a1 polyclonal antibody  (Proteintech)


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    Proteintech slc25a1 polyclonal antibody
    ( A ) Venn diagram showing differential genes in pairs among the three groups. Log2 FC (Fold Change) > 1.2 or < –1.2, q value < 0.05. ( B ) Histogram showing pairwise comparison of differential gene expression (DEG) from bulk RNA-seq among the CTRL, SEC, and WOI groups. q value < 0.05, |logFC| > 1. ( C ) PCA plot computed with differentially expressed proteins in the micro proteomics of endometrial assembloids belonging to the CTRL, SEC, and WOI groups. ( D ) Venn diagram showing differential proteins in pairs among the three groups. Log2 FC > 1.2 or < –1.2, q value < 0.05. ( E ) Histogram showing pairwise comparison of differential proteins in microproteomics among the CTRL, SEC, and WOI groups. ( F ) Scatterplot depicting the correlation between the transcriptome and proteome as for the WOI group and CTRL group. For the transcriptome, FC > 2 and p value < 0.05 were defined as significantly upregulated. For the proteome, FC > 1.2 and p value < 0.05 were defined as significantly upregulated. ( G ) Circle diagram showing the functions of genes upregulated in both the transcriptome and proteome as for the WOI group compared to the CTRL group. ( H ) Verification of hypoxia response by the expression levels of HIF1α. Scale bar = 50 μm. * p ≤0.05, ** p ≤0.005.n = 5, with 4–5 sections collected from each sample. ( I ) Verification of lipid metabolism by the expression levels of <t>SLC25A1.</t> Scale bar = 50 μm. **** p ≤0.0001. n = 5, with 3–5 sections collected from each sample.
    Slc25a1 Polyclonal Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 36 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/slc25a1+polyclonal+antibody/pmc13043174-20-2-8?v=Proteintech
    Average 93 stars, based on 36 article reviews
    slc25a1 polyclonal antibody - by Bioz Stars, 2026-08
    93/100 stars

    Images

    1) Product Images from "Human receptive endometrial assembloid for deciphering the implantation window"

    Article Title: Human receptive endometrial assembloid for deciphering the implantation window

    Journal: eLife

    doi: 10.7554/eLife.90729

    ( A ) Venn diagram showing differential genes in pairs among the three groups. Log2 FC (Fold Change) > 1.2 or < –1.2, q value < 0.05. ( B ) Histogram showing pairwise comparison of differential gene expression (DEG) from bulk RNA-seq among the CTRL, SEC, and WOI groups. q value < 0.05, |logFC| > 1. ( C ) PCA plot computed with differentially expressed proteins in the micro proteomics of endometrial assembloids belonging to the CTRL, SEC, and WOI groups. ( D ) Venn diagram showing differential proteins in pairs among the three groups. Log2 FC > 1.2 or < –1.2, q value < 0.05. ( E ) Histogram showing pairwise comparison of differential proteins in microproteomics among the CTRL, SEC, and WOI groups. ( F ) Scatterplot depicting the correlation between the transcriptome and proteome as for the WOI group and CTRL group. For the transcriptome, FC > 2 and p value < 0.05 were defined as significantly upregulated. For the proteome, FC > 1.2 and p value < 0.05 were defined as significantly upregulated. ( G ) Circle diagram showing the functions of genes upregulated in both the transcriptome and proteome as for the WOI group compared to the CTRL group. ( H ) Verification of hypoxia response by the expression levels of HIF1α. Scale bar = 50 μm. * p ≤0.05, ** p ≤0.005.n = 5, with 4–5 sections collected from each sample. ( I ) Verification of lipid metabolism by the expression levels of SLC25A1. Scale bar = 50 μm. **** p ≤0.0001. n = 5, with 3–5 sections collected from each sample.
    Figure Legend Snippet: ( A ) Venn diagram showing differential genes in pairs among the three groups. Log2 FC (Fold Change) > 1.2 or < –1.2, q value < 0.05. ( B ) Histogram showing pairwise comparison of differential gene expression (DEG) from bulk RNA-seq among the CTRL, SEC, and WOI groups. q value < 0.05, |logFC| > 1. ( C ) PCA plot computed with differentially expressed proteins in the micro proteomics of endometrial assembloids belonging to the CTRL, SEC, and WOI groups. ( D ) Venn diagram showing differential proteins in pairs among the three groups. Log2 FC > 1.2 or < –1.2, q value < 0.05. ( E ) Histogram showing pairwise comparison of differential proteins in microproteomics among the CTRL, SEC, and WOI groups. ( F ) Scatterplot depicting the correlation between the transcriptome and proteome as for the WOI group and CTRL group. For the transcriptome, FC > 2 and p value < 0.05 were defined as significantly upregulated. For the proteome, FC > 1.2 and p value < 0.05 were defined as significantly upregulated. ( G ) Circle diagram showing the functions of genes upregulated in both the transcriptome and proteome as for the WOI group compared to the CTRL group. ( H ) Verification of hypoxia response by the expression levels of HIF1α. Scale bar = 50 μm. * p ≤0.05, ** p ≤0.005.n = 5, with 4–5 sections collected from each sample. ( I ) Verification of lipid metabolism by the expression levels of SLC25A1. Scale bar = 50 μm. **** p ≤0.0001. n = 5, with 3–5 sections collected from each sample.

    Techniques Used: Comparison, Gene Expression, RNA Sequencing, Expressing



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    ( A ) Venn diagram showing differential genes in pairs among the three groups. Log2 FC (Fold Change) > 1.2 or < –1.2, q value < 0.05. ( B ) Histogram showing pairwise comparison of differential gene expression (DEG) from bulk RNA-seq among the CTRL, SEC, and WOI groups. q value < 0.05, |logFC| > 1. ( C ) PCA plot computed with differentially expressed proteins in the micro proteomics of endometrial assembloids belonging to the CTRL, SEC, and WOI groups. ( D ) Venn diagram showing differential proteins in pairs among the three groups. Log2 FC > 1.2 or < –1.2, q value < 0.05. ( E ) Histogram showing pairwise comparison of differential proteins in microproteomics among the CTRL, SEC, and WOI groups. ( F ) Scatterplot depicting the correlation between the transcriptome and proteome as for the WOI group and CTRL group. For the transcriptome, FC > 2 and p value < 0.05 were defined as significantly upregulated. For the proteome, FC > 1.2 and p value < 0.05 were defined as significantly upregulated. ( G ) Circle diagram showing the functions of genes upregulated in both the transcriptome and proteome as for the WOI group compared to the CTRL group. ( H ) Verification of hypoxia response by the expression levels of HIF1α. Scale bar = 50 μm. * p ≤0.05, ** p ≤0.005.n = 5, with 4–5 sections collected from each sample. ( I ) Verification of lipid metabolism by the expression levels of <t>SLC25A1.</t> Scale bar = 50 μm. **** p ≤0.0001. n = 5, with 3–5 sections collected from each sample.
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    ( A ) Venn diagram showing differential genes in pairs among the three groups. Log2 FC (Fold Change) > 1.2 or < –1.2, q value < 0.05. ( B ) Histogram showing pairwise comparison of differential gene expression (DEG) from bulk RNA-seq among the CTRL, SEC, and WOI groups. q value < 0.05, |logFC| > 1. ( C ) PCA plot computed with differentially expressed proteins in the micro proteomics of endometrial assembloids belonging to the CTRL, SEC, and WOI groups. ( D ) Venn diagram showing differential proteins in pairs among the three groups. Log2 FC > 1.2 or < –1.2, q value < 0.05. ( E ) Histogram showing pairwise comparison of differential proteins in microproteomics among the CTRL, SEC, and WOI groups. ( F ) Scatterplot depicting the correlation between the transcriptome and proteome as for the WOI group and CTRL group. For the transcriptome, FC > 2 and p value < 0.05 were defined as significantly upregulated. For the proteome, FC > 1.2 and p value < 0.05 were defined as significantly upregulated. ( G ) Circle diagram showing the functions of genes upregulated in both the transcriptome and proteome as for the WOI group compared to the CTRL group. ( H ) Verification of hypoxia response by the expression levels of HIF1α. Scale bar = 50 μm. * p ≤0.05, ** p ≤0.005.n = 5, with 4–5 sections collected from each sample. ( I ) Verification of lipid metabolism by the expression levels of <t>SLC25A1.</t> Scale bar = 50 μm. **** p ≤0.0001. n = 5, with 3–5 sections collected from each sample.
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    Image Search Results


    ( A ) Venn diagram showing differential genes in pairs among the three groups. Log2 FC (Fold Change) > 1.2 or < –1.2, q value < 0.05. ( B ) Histogram showing pairwise comparison of differential gene expression (DEG) from bulk RNA-seq among the CTRL, SEC, and WOI groups. q value < 0.05, |logFC| > 1. ( C ) PCA plot computed with differentially expressed proteins in the micro proteomics of endometrial assembloids belonging to the CTRL, SEC, and WOI groups. ( D ) Venn diagram showing differential proteins in pairs among the three groups. Log2 FC > 1.2 or < –1.2, q value < 0.05. ( E ) Histogram showing pairwise comparison of differential proteins in microproteomics among the CTRL, SEC, and WOI groups. ( F ) Scatterplot depicting the correlation between the transcriptome and proteome as for the WOI group and CTRL group. For the transcriptome, FC > 2 and p value < 0.05 were defined as significantly upregulated. For the proteome, FC > 1.2 and p value < 0.05 were defined as significantly upregulated. ( G ) Circle diagram showing the functions of genes upregulated in both the transcriptome and proteome as for the WOI group compared to the CTRL group. ( H ) Verification of hypoxia response by the expression levels of HIF1α. Scale bar = 50 μm. * p ≤0.05, ** p ≤0.005.n = 5, with 4–5 sections collected from each sample. ( I ) Verification of lipid metabolism by the expression levels of SLC25A1. Scale bar = 50 μm. **** p ≤0.0001. n = 5, with 3–5 sections collected from each sample.

    Journal: eLife

    Article Title: Human receptive endometrial assembloid for deciphering the implantation window

    doi: 10.7554/eLife.90729

    Figure Lengend Snippet: ( A ) Venn diagram showing differential genes in pairs among the three groups. Log2 FC (Fold Change) > 1.2 or < –1.2, q value < 0.05. ( B ) Histogram showing pairwise comparison of differential gene expression (DEG) from bulk RNA-seq among the CTRL, SEC, and WOI groups. q value < 0.05, |logFC| > 1. ( C ) PCA plot computed with differentially expressed proteins in the micro proteomics of endometrial assembloids belonging to the CTRL, SEC, and WOI groups. ( D ) Venn diagram showing differential proteins in pairs among the three groups. Log2 FC > 1.2 or < –1.2, q value < 0.05. ( E ) Histogram showing pairwise comparison of differential proteins in microproteomics among the CTRL, SEC, and WOI groups. ( F ) Scatterplot depicting the correlation between the transcriptome and proteome as for the WOI group and CTRL group. For the transcriptome, FC > 2 and p value < 0.05 were defined as significantly upregulated. For the proteome, FC > 1.2 and p value < 0.05 were defined as significantly upregulated. ( G ) Circle diagram showing the functions of genes upregulated in both the transcriptome and proteome as for the WOI group compared to the CTRL group. ( H ) Verification of hypoxia response by the expression levels of HIF1α. Scale bar = 50 μm. * p ≤0.05, ** p ≤0.005.n = 5, with 4–5 sections collected from each sample. ( I ) Verification of lipid metabolism by the expression levels of SLC25A1. Scale bar = 50 μm. **** p ≤0.0001. n = 5, with 3–5 sections collected from each sample.

    Article Snippet: Antibody , SLC25A1 Polyclonal antibody (Rabbit polyclonal) , Proteintech , Cat#: 15235–1-AP RRID: AB_2254794 , IF (1:500).

    Techniques: Comparison, Gene Expression, RNA Sequencing, Expressing

    Journal: The EMBO Journal

    Article Title: Hypoxia promotes osteogenesis by facilitating acetyl‐CoA ‐mediated mitochondrial–nuclear communication

    doi: 10.15252/embj.2022111239

    Figure Lengend Snippet:

    Article Snippet: Rabbit anti‐Citrate carrier, Polyclonal (1:500) , ProteinTech , #15235‐1‐AP.

    Techniques: Transgenic Assay, Isolation, Recombinant, Generated, Software, Bicinchoninic Acid Protein Assay, RNA Extraction, Reverse Transcription, Ligation, Mass Spectrometry, Liquid Chromatography, Microscopy

    Irradiation induces alterations to the extracellular matrix and mitochondrial metabolism. (A) Immunohistochemistry staining analysis of Col1a1 and Col3a1 in the heart tissues. Magnification, ×400. (B) Western blotting and (C) semi-quantitative analysis of Col1a1, Col3a1, Vimentin and CTGF. (D) Western blotting and (E) semi-quantitative analysis of metabolism related genes Fasn and Slc25al. Relative protein levels of Col1a1, Col3a1, Vimentin, CTGF, Fasn and Slc25al were normalized to Tubulin. (F) Electron micrographs of the cardiac mitochondria from the mice in sham-irradiated and 5-month groups after 16 Gy radiation. Left magnification, ×3,000; Middle magnification, ×6,000; Right magnification, ×20,000. Green arrows show the myofilaments with fuzzy boundaries. Red arrows show swollen mitochondria with cavitation. Measurement of (G) ATP levels and (H) lactic acid concentration in the sham-irradiated and 5-month mice heart tissues. *P<0.05, **P<0.01, ***P<0.001; # P<0.05; n=3 per group. Col1a1, collagen type 1 α 1 chain; Col3a1, collagen type III α 1 chain; CTGF, CCCTC-binding factor; Fasn, fatty acid synthase; Slc25a1, solute carrier family 25 member 1.

    Journal: Molecular Medicine Reports

    Article Title: Radiation-induced dysfunction of energy metabolism in the heart results in the fibrosis of cardiac tissues

    doi: 10.3892/mmr.2021.12482

    Figure Lengend Snippet: Irradiation induces alterations to the extracellular matrix and mitochondrial metabolism. (A) Immunohistochemistry staining analysis of Col1a1 and Col3a1 in the heart tissues. Magnification, ×400. (B) Western blotting and (C) semi-quantitative analysis of Col1a1, Col3a1, Vimentin and CTGF. (D) Western blotting and (E) semi-quantitative analysis of metabolism related genes Fasn and Slc25al. Relative protein levels of Col1a1, Col3a1, Vimentin, CTGF, Fasn and Slc25al were normalized to Tubulin. (F) Electron micrographs of the cardiac mitochondria from the mice in sham-irradiated and 5-month groups after 16 Gy radiation. Left magnification, ×3,000; Middle magnification, ×6,000; Right magnification, ×20,000. Green arrows show the myofilaments with fuzzy boundaries. Red arrows show swollen mitochondria with cavitation. Measurement of (G) ATP levels and (H) lactic acid concentration in the sham-irradiated and 5-month mice heart tissues. *P<0.05, **P<0.01, ***P<0.001; # P<0.05; n=3 per group. Col1a1, collagen type 1 α 1 chain; Col3a1, collagen type III α 1 chain; CTGF, CCCTC-binding factor; Fasn, fatty acid synthase; Slc25a1, solute carrier family 25 member 1.

    Article Snippet: The primary antibodies used in the present study were: Anti-Col1a1 polyclonal antibody (1:1,000; Wuhan Boster Biological Technology, Ltd.; cat. no. BA0325), anti-Col3a1 monoclonal antibody (1:1,000; Wuhan Boster Biological Technology, Ltd.; cat. no. M00788), anti-CCCTC-binding factor (CTGF) polyclonal antibody (1:1,000; Wuhan Boster Biological Technology, Ltd.; cat. no. PB0570), anti-vimentin (VIM) monoclonal antibody (1:1,000; Wuhan Boster Biological Technology, Ltd.; cat. no. BM0135), anti-fatty acid synthase (Fasn) monoclonal antibody (1:1,000; Wuhan Boster Biological Technology, Ltd.; cat. no. BM4865), anti-solute carrier family 25 member 1 (Slc25a1) polyclonal antibody (1:1,000; Wuhan Boster Biological Technology, Ltd.; cat. no. A05995-2) and anti-α-tubulin monoclonal antibody (1:1,000; Wuhan Boster Biological Technology, Ltd.; cat. no. M03989-2).

    Techniques: Irradiation, Immunohistochemistry, Staining, Western Blot, Concentration Assay, Binding Assay

    Upregulation of metabolism-related proteins in the mouse heart 5 months after exposure to ionizing radiation.

    Journal: Molecular Medicine Reports

    Article Title: Radiation-induced dysfunction of energy metabolism in the heart results in the fibrosis of cardiac tissues

    doi: 10.3892/mmr.2021.12482

    Figure Lengend Snippet: Upregulation of metabolism-related proteins in the mouse heart 5 months after exposure to ionizing radiation.

    Article Snippet: The primary antibodies used in the present study were: Anti-Col1a1 polyclonal antibody (1:1,000; Wuhan Boster Biological Technology, Ltd.; cat. no. BA0325), anti-Col3a1 monoclonal antibody (1:1,000; Wuhan Boster Biological Technology, Ltd.; cat. no. M00788), anti-CCCTC-binding factor (CTGF) polyclonal antibody (1:1,000; Wuhan Boster Biological Technology, Ltd.; cat. no. PB0570), anti-vimentin (VIM) monoclonal antibody (1:1,000; Wuhan Boster Biological Technology, Ltd.; cat. no. BM0135), anti-fatty acid synthase (Fasn) monoclonal antibody (1:1,000; Wuhan Boster Biological Technology, Ltd.; cat. no. BM4865), anti-solute carrier family 25 member 1 (Slc25a1) polyclonal antibody (1:1,000; Wuhan Boster Biological Technology, Ltd.; cat. no. A05995-2) and anti-α-tubulin monoclonal antibody (1:1,000; Wuhan Boster Biological Technology, Ltd.; cat. no. M03989-2).

    Techniques: