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Santa Cruz Biotechnology mta1
Mta1, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 159 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mta1/MTA1+Antibody/pmc12704216-52-9-15
Average 93 stars, based on 159 article reviews
mta1 - by Bioz Stars, 2026-10
93/100 stars

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Related Articles

other:

Article Title: Nicotinic Acid-Mediated Modulation of Metastasis-Associated Protein 1 Methylation and Inflammation in Brain Arteriovenous Malformation.
Article Snippet: We used the following antibodies for the experiments: p-RELA/NFκB p65 antibody (Cat: sc-136548, Santa Cruz Biotechnology, TX, USA), MTA1 (Cat: sc-373765, Santa Cruz), HRP-conjugated Affinipure Goat Anti-Rabbit IgG (Cat: SA00001-2, Proteintech, Wuhan, China), HRP-conjugated Affinipure Goat Anti-Mouse IgG (Cat: SA00001-1, Proteintech), and β-actin Antibody (Cat: AF7018, Affinity, Jiangsu, China).

Article Title: Leptin-Upregulated Metastasis-Associated Protein 1 Promotes Vasculogenic Mimicry in Breast Cancer Cells
Article Snippet: MTA1 , Santa Cruz , 1:500 , SC-17773.

Incubation:

Article Title: Validation of survivin and HMGA2 as biomarkers for cisplatin resistance in bladder cancer.
Article Snippet: Objectives: Cisplatin-based chemotherapy represents the gold standard in the treatment of advanced bladder cancer (BC) both in the neoadjuvant and adjuvant setting.. Since novel immunooncologic agents are available for cisplatin-resistant or ineligible patients, biological markers for the prediction of cisplatin resistance become more important in treatment decisions.. Therefore, we aimed to assess the therapy predictive value of 8 promising tissue biomarkers with regard to cisplatin therapy.

Article Title: Membranous CD44v6 is upregulated as an early event in colorectal cancer: Downregulation is associated with circulating tumor cells and poor prognosis
Article Snippet: .. Sections were incubated at 4°C overnight with the following primary antibodies at the specified dilutions mCD44v6 (Bio-Rad MCA1730, dilution 1:100), MTA1 (Santa Cruz Biotechnology SC-17773 dilution 1:200). .. The detection was performed according to the ChemMateEnVision system (DAKO EnVision Detection Systems, Peroxidase/DAB, Rabbit/Mouse) protocol.

Immunohistochemistry:

Article Title: Validation of survivin and HMGA2 as biomarkers for cisplatin resistance in bladder cancer.
Article Snippet: Objectives: Cisplatin-based chemotherapy represents the gold standard in the treatment of advanced bladder cancer (BC) both in the neoadjuvant and adjuvant setting.. Since novel immunooncologic agents are available for cisplatin-resistant or ineligible patients, biological markers for the prediction of cisplatin resistance become more important in treatment decisions.. Therefore, we aimed to assess the therapy predictive value of 8 promising tissue biomarkers with regard to cisplatin therapy.

Staining:

Article Title: Validation of survivin and HMGA2 as biomarkers for cisplatin resistance in bladder cancer.
Article Snippet: Objectives: Cisplatin-based chemotherapy represents the gold standard in the treatment of advanced bladder cancer (BC) both in the neoadjuvant and adjuvant setting.. Since novel immunooncologic agents are available for cisplatin-resistant or ineligible patients, biological markers for the prediction of cisplatin resistance become more important in treatment decisions.. Therefore, we aimed to assess the therapy predictive value of 8 promising tissue biomarkers with regard to cisplatin therapy.



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Santa Cruz Biotechnology mta1 crispr activation plasmid
Figure 1. Leptin upregulates <t>MTA1</t> expression in human breast cancer cells. MTA1 mRNA expression was analyzed using qPCR in MDA-MB-231 (A) and Hs 578T cells (B) after leptin treatment for 24 h. Results are expressed as mean ± SD; * p < 0.05 and ** p < 0.01 vs. untreated control. MTA1 protein expression was assessed using Western blot in MDA-MB-231 (C) and Hs 578T cells (D) after 24 h of leptin treatment.
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Figure 1. Leptin upregulates MTA1 expression in human breast cancer cells. MTA1 mRNA expression was analyzed using qPCR in MDA-MB-231 (A) and Hs 578T cells (B) after leptin treatment for 24 h. Results are expressed as mean ± SD; * p < 0.05 and ** p < 0.01 vs. untreated control. MTA1 protein expression was assessed using Western blot in MDA-MB-231 (C) and Hs 578T cells (D) after 24 h of leptin treatment.

Journal: International Journal of Molecular Sciences

Article Title: Leptin-Upregulated Metastasis-Associated Protein 1 Promotes Vasculogenic Mimicry in Breast Cancer Cells

doi: 10.3390/ijms26125726

Figure Lengend Snippet: Figure 1. Leptin upregulates MTA1 expression in human breast cancer cells. MTA1 mRNA expression was analyzed using qPCR in MDA-MB-231 (A) and Hs 578T cells (B) after leptin treatment for 24 h. Results are expressed as mean ± SD; * p < 0.05 and ** p < 0.01 vs. untreated control. MTA1 protein expression was assessed using Western blot in MDA-MB-231 (C) and Hs 578T cells (D) after 24 h of leptin treatment.

Article Snippet: MDA-MB-231 cells (1.5 × 105) and Hs 578T cells (2.0 × 105) were cultured under optimal conditions and transfected with 1 μg of the control or 0.5 μg of the MTA1 CRISPR activation plasmid (Santa Cruz, Danvers, MA, USA) for 48 h. Transfection was performed using the UltraCruz transfection reagent (Santa Cruz), according to the manufacturer’s protocol.

Techniques: Expressing, Control, Western Blot

Figure 2. Leptin upregulates MTA1 expression via the Ob-R/STAT3 pathway in human breast cancer cells. MTA1 protein expression was evaluated using Western blot in MDA-MB-231 (A,C) and Hs 578T cells (B,D) after 24 h of leptin treatment in the presence or absence of Ob-R BP (A,B) or AG490 (C,D).

Journal: International Journal of Molecular Sciences

Article Title: Leptin-Upregulated Metastasis-Associated Protein 1 Promotes Vasculogenic Mimicry in Breast Cancer Cells

doi: 10.3390/ijms26125726

Figure Lengend Snippet: Figure 2. Leptin upregulates MTA1 expression via the Ob-R/STAT3 pathway in human breast cancer cells. MTA1 protein expression was evaluated using Western blot in MDA-MB-231 (A,C) and Hs 578T cells (B,D) after 24 h of leptin treatment in the presence or absence of Ob-R BP (A,B) or AG490 (C,D).

Article Snippet: MDA-MB-231 cells (1.5 × 105) and Hs 578T cells (2.0 × 105) were cultured under optimal conditions and transfected with 1 μg of the control or 0.5 μg of the MTA1 CRISPR activation plasmid (Santa Cruz, Danvers, MA, USA) for 48 h. Transfection was performed using the UltraCruz transfection reagent (Santa Cruz), according to the manufacturer’s protocol.

Techniques: Expressing, Western Blot

Figure 3. MTA1 overexpression promotes VM in human breast cancer cells. MDA-MB-231 (A,C,E) and Hs 578T cells (B,D,F) were transfected with the MTA1 CRISPR activation plasmid for 48 h. MTA1 protein expression was assessed using Western blot in MDA-MB-231 (A) and Hs 578T cells (B). VM was performed using a 3D culture assay for 16 h in MDA-MB-231 (C) and Hs 578T cells (D) (40× mag- nification; scale bar = 500 µm). Results are expressed as mean ± SD; *** p < 0.001 vs. control plasmid. Expression of VM-related proteins was evaluated using Western blot in MDA-MB-231 (E) and Hs 578T cells (F).

Journal: International Journal of Molecular Sciences

Article Title: Leptin-Upregulated Metastasis-Associated Protein 1 Promotes Vasculogenic Mimicry in Breast Cancer Cells

doi: 10.3390/ijms26125726

Figure Lengend Snippet: Figure 3. MTA1 overexpression promotes VM in human breast cancer cells. MDA-MB-231 (A,C,E) and Hs 578T cells (B,D,F) were transfected with the MTA1 CRISPR activation plasmid for 48 h. MTA1 protein expression was assessed using Western blot in MDA-MB-231 (A) and Hs 578T cells (B). VM was performed using a 3D culture assay for 16 h in MDA-MB-231 (C) and Hs 578T cells (D) (40× mag- nification; scale bar = 500 µm). Results are expressed as mean ± SD; *** p < 0.001 vs. control plasmid. Expression of VM-related proteins was evaluated using Western blot in MDA-MB-231 (E) and Hs 578T cells (F).

Article Snippet: MDA-MB-231 cells (1.5 × 105) and Hs 578T cells (2.0 × 105) were cultured under optimal conditions and transfected with 1 μg of the control or 0.5 μg of the MTA1 CRISPR activation plasmid (Santa Cruz, Danvers, MA, USA) for 48 h. Transfection was performed using the UltraCruz transfection reagent (Santa Cruz), according to the manufacturer’s protocol.

Techniques: Over Expression, Transfection, CRISPR, Activation Assay, Plasmid Preparation, Expressing, Western Blot, Control

Figure 4. MTA1 silencing inhibits leptin-induced VM in human breast cancer cells. MDA-MB- 231 (A,C,E) and Hs 578T cells (B,D,F) were treated with leptin 48 h after transfection with MTA1 siRNA. MTA1 protein expression was evaluated using Western blot in MDA-MB-231 (A) and Hs 578T cells (B). VM was performed using a 3D culture assay for 16 h in MDA-MB-231 (C) and Hs 578T cells (D) (40× magnification; scale bar = 250 µm). Results are expressed as mean ± SD; *** p < 0.001 vs. untreated control; ### p < 0.001 vs. control siRNA. Expression of VM-related proteins was evaluated using Western blot in MDA-MB-231 (E) and Hs 578T cells (F).

Journal: International Journal of Molecular Sciences

Article Title: Leptin-Upregulated Metastasis-Associated Protein 1 Promotes Vasculogenic Mimicry in Breast Cancer Cells

doi: 10.3390/ijms26125726

Figure Lengend Snippet: Figure 4. MTA1 silencing inhibits leptin-induced VM in human breast cancer cells. MDA-MB- 231 (A,C,E) and Hs 578T cells (B,D,F) were treated with leptin 48 h after transfection with MTA1 siRNA. MTA1 protein expression was evaluated using Western blot in MDA-MB-231 (A) and Hs 578T cells (B). VM was performed using a 3D culture assay for 16 h in MDA-MB-231 (C) and Hs 578T cells (D) (40× magnification; scale bar = 250 µm). Results are expressed as mean ± SD; *** p < 0.001 vs. untreated control; ### p < 0.001 vs. control siRNA. Expression of VM-related proteins was evaluated using Western blot in MDA-MB-231 (E) and Hs 578T cells (F).

Article Snippet: MDA-MB-231 cells (1.5 × 105) and Hs 578T cells (2.0 × 105) were cultured under optimal conditions and transfected with 1 μg of the control or 0.5 μg of the MTA1 CRISPR activation plasmid (Santa Cruz, Danvers, MA, USA) for 48 h. Transfection was performed using the UltraCruz transfection reagent (Santa Cruz), according to the manufacturer’s protocol.

Techniques: Transfection, Expressing, Western Blot, Control