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Alomone Labs
anti cav1 2 Anti Cav1 2, supplied by Alomone Labs, 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/product/creatine+transporter+1/us11433116-437-10-12?v=Alomone+Labs Average 91 stars, based on 1 article reviews
anti cav1 2 - by Bioz Stars,
2026-07
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Proteintech
anti slc6a8 antibody ![]() Anti Slc6a8 Antibody, 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/product/creatine+transporter+1/pmc12963567-35-7-12?v=Proteintech Average 93 stars, based on 1 article reviews
anti slc6a8 antibody - by Bioz Stars,
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Incyte corporation
creatine transporter 1 ![]() Creatine Transporter 1, supplied by Incyte 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/product/creatine+transporter+1/pm11578147-260-22-39?v=Incyte+corporation Average 90 stars, based on 1 article reviews
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This antibody is expected to recognize all reported isoforms (NP_005620.1; NP_001136277.1; NP_001136278.1).
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Creatine transporter 1 Antibody is a Goat Polyclonal antibody against Creatine transporter 1
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Image Search Results
Journal: Journal of Cancer Research and Clinical Oncology
Article Title: Targeting SLC6A8 suppresses tumor growth and enhances ferroptosis in hepatocellular carcinoma
doi: 10.1007/s00432-026-06442-8
Figure Lengend Snippet: SLC6A8 is upregulated in HCC and correlated with poor prognosis of HCC patients. A Expression box plot of SLC6A8 in HCC patients from the GEPIA online database. B The correlation between SLC6A8 expression and 5-year overall survival analyzed by Kaplan-Meier plotter. C The fold change of SLC6A8 mRNA levels in HCC tumor tissues compared to matched para-cancerous tissues using qRT-PCR. C: cancer tissues; N: adjacent normal tissues. And Percentage of SLC6A8 expression alteration in 30 paired of HCC samples. Upregulated: C/ N > 1.5; Downregulated: C/ N < 0.67. D Representative IHC staining images displayed different levels of SLC6A8. Scale bars, up: 200 μm; down: 50 μm. E The AOD values of SLC6A8 protein in tumor and normal tissues from TMA. F Quantification of SLC6A8 expression in tumor and normal tissues from TMA. G The overall survival curve analyzed by Kaplan-Meier for HCC patients with a high or low level of SLC6A8 protein level. * P < 0.05, ** P < 0.01
Article Snippet: Immunohistochemistry (IHC) was carried out with an
Techniques: Expressing, Quantitative RT-PCR, Immunohistochemistry
Journal: Journal of Cancer Research and Clinical Oncology
Article Title: Targeting SLC6A8 suppresses tumor growth and enhances ferroptosis in hepatocellular carcinoma
doi: 10.1007/s00432-026-06442-8
Figure Lengend Snippet: SLC6A8 knockdown suppresses HCC cell growth in vitro. A The efficiency of siSLC6A8 transfection in HCC cells assessed by Western blotting. B CCK-8 assays for HCC cells transfected with siSLC6A8-1, siSLC6A8-2 or siNC. C Colony formation assays for HCC cells transfected with siSLC6A8-1, siSLC6A8-2 or siNC. D Transwell migration assays for HCC cells transfected with siSLC6A8-1, siSLC6A8-2 or siNC. Scale bars, 100 μm. * P < 0.05, ** P < 0.01
Article Snippet: Immunohistochemistry (IHC) was carried out with an
Techniques: Knockdown, In Vitro, Transfection, Western Blot, CCK-8 Assay, Migration
Journal: Journal of Cancer Research and Clinical Oncology
Article Title: Targeting SLC6A8 suppresses tumor growth and enhances ferroptosis in hepatocellular carcinoma
doi: 10.1007/s00432-026-06442-8
Figure Lengend Snippet: SLC6A8 inhibitor RGX-202 exhibits potent antitumor effects in HCC cells. A Cell viability for HCC cells treated with 0, 10 and 20mM RGX-202 assessed by CCK-8 assays B Effect on cell proliferation of RGX202 in HCC cells assessed by Colony formation assays exposed to 0, 5 and 10mM RGX-202. * P < 0.05, ** P < 0.01
Article Snippet: Immunohistochemistry (IHC) was carried out with an
Techniques: CCK-8 Assay
Journal: Journal of Cancer Research and Clinical Oncology
Article Title: Targeting SLC6A8 suppresses tumor growth and enhances ferroptosis in hepatocellular carcinoma
doi: 10.1007/s00432-026-06442-8
Figure Lengend Snippet: Targeting SLC6A8 suppresses tumorigenicity of HCC cells in nude mice model. A HCC-LM3 cells with stable SLC6A8 knockdown used for Subcutaneous xenograft model of nude mice ( n = 5 per group). Representative images of tumors (left), tumor weight (middle), and tumor volume (right). B xenografts from HCC-LM3 cells with or without the treatment of RGX-202 (500 mg/kg, orally gavage once a day, n = 5 per group). Representative images of tumors (left), tumor weight (middle), and tumor volume (right). * P < 0.05, ** P < 0.01
Article Snippet: Immunohistochemistry (IHC) was carried out with an
Techniques: Knockdown
Journal: Journal of Cancer Research and Clinical Oncology
Article Title: Targeting SLC6A8 suppresses tumor growth and enhances ferroptosis in hepatocellular carcinoma
doi: 10.1007/s00432-026-06442-8
Figure Lengend Snippet: SLC6A8 inhibition sensitizes HCC cells to ferroptosis. A Cell growth curve of Huh7 and HCC-LM3 shSLC6A8 and shNC treated with vehicle control, and 0.25μM RSL3 or 0.25μM RSL3 plus 1μM Fer-1 using CCK-8 assays. B Intracellular MDA levels of Huh7 shSLC6A8 and shNC treated with vehicle control, 1μM RSL3, and 1μM RSL3 plus 1μM Fer-1 for 24h. C – D Intracellular ROS content of Huh7 shSLC6A8 and shNC treated with control, 1μM RSL3, and 1μM RSL3 plus 1μM Fer-1 observed using fluorescence microscope and quantified using flow cytometry. Scale bar: 100µm. E xenografts from HCC-LM3 cells with treatment of control, RGX-202 (500mg/kg, orally gavage once a day), RSL3 (10mg/kg, administrated intraperitoneally every other day), or combination of RGX-202 and RSL3. Representative images of tumors (left), tumor weight (middle), and tumor volume (right). * P < 0.05, ** P < 0.01
Article Snippet: Immunohistochemistry (IHC) was carried out with an
Techniques: Inhibition, Control, CCK-8 Assay, Fluorescence, Microscopy, Flow Cytometry