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TissueArray.com LLC tissue microarray slides
Tissue Microarray Slides, supplied by TissueArray.com LLC, 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/melanoma+tissue+microarray+slides/tissue+microarray+slides/pmc03511679-183-0-6
Average 90 stars, based on 1 article reviews
tissue microarray slides - by Bioz Stars, 2026-11
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Article Title: Activin B and Activin C Have Opposing Effects on Prostate Cancer Progression and Cell Growth
Article Snippet: Tissue microarray (TMA) slides (PR483b, PR752, PR8011a; US Biomax, Derwood, MD, USA) containing cores from human cases of primary prostate adenocarcinoma (134 cores, 88 cases) and normal prostate tissue (15 cores, 13 cases) were immuno-stained following methods described by Marino et al. [ ].

Article Title: Nuclear localization of APLF facilitates breast cancer metastasis.
Article Snippet: Most breast cancer deaths result from metastases.. We previously reported that DNA repair factor and histone chaperone Aprataxin PNK-like Factor (APLF) is involved in EMT-associated metastasis of triple negative breast cancer (TNBC) cells.. However, non-metastatic cells also expressed APLF, the implications of which in disease advancement remain uncertain.

Article Title: PROX1 is a regulator of neuroendocrine-related gene expression in lung carcinoid.
Article Snippet: Lung neuroendocrine neoplasms (NENs) are a diverse group of tumors characterized by neuroendocrine (NE) differentiation.. Among lung NENs, lung carcinoid (LC) is a rare tumor with unique characteristics.. Recent research has highlighted the importance of transcription factors (TFs) in establishing gene expression programs in lung NENs such as small cell lung carcinoma.

Microarray:

Article Title: Unlocking Overexpressed Membrane Proteins to Guide Breast Cancer Precision Medicine
Article Snippet: .. BC tissue microarray slides (US Biomax, ref.: BC081116d/ (Rockville, MD, USA)) were kept at 60 °C for 2 h before use. ..

Article Title: The Molecular Pathogenesis of Tumor-Suppressive miR-486-5p and miR-486-3p Target Genes: GINS4 Facilitates Aggressiveness in Lung Adenocarcinoma
Article Snippet: .. GINS4 expression was evaluated by immunohistochemical staining using tissue microarray slides (catalog no.: LC811a, US Biomax, Inc. Derwood, MD, USA). .. The VECTASTAIN Universal Elite ABC Kit (catalog no.: PK-6200, Vector Laboratories, Burlingame, CA, USA) was used for blocking, the primary antibody reaction, the secondary antibody reaction, and the binding of avidin to the biotin complex.

Article Title: Aptamer-Based Recognition of Breast Tumor Cells: A New Era for Breast Cancer Diagnosis.
Article Snippet: .. The assays using clinical specimens from patients with breast cancer were performed with tissue microarray slides purchased from US Biomax Inc. (Rockville, MD, USA) (ref.: BR1008b). ..

Article Title: HOXC6 drives a therapeutically targetable pancreatic cancer growth and metastasis pathway by regulating MSK1 and PPP2R2B
Article Snippet: Tissue microarray slide (PDAC and matched normal pancreas tissue) , US Biomax, Inc. , Cat# HPan-Ade150CS-02. .. Tissue microarray slide (PDAC and matched normal pancreas tissue) , US Biomax, Inc. , Cat# PA601. ..

Article Title: Minichromosome maintenance proteins in lung adenocarcinoma: Clinical significance and therapeutic targets.
Article Snippet: .. Tissue microarray slides (catalog no.: LC811a; US Biomax, Inc., Derwood, MD, USA) were used for immunohistochemical staining. .. Blocking, the primary antibody reaction, secondary antibody reaction, and binding of avidin to the biotin complex were conducted using a VECTASTAIN Universal Elite ABC Kit (Vector Laboratories, Burlingame, CA, USA) according to the manufacturer’s protocol.

Expressing:

Article Title: The Molecular Pathogenesis of Tumor-Suppressive miR-486-5p and miR-486-3p Target Genes: GINS4 Facilitates Aggressiveness in Lung Adenocarcinoma
Article Snippet: .. GINS4 expression was evaluated by immunohistochemical staining using tissue microarray slides (catalog no.: LC811a, US Biomax, Inc. Derwood, MD, USA). .. The VECTASTAIN Universal Elite ABC Kit (catalog no.: PK-6200, Vector Laboratories, Burlingame, CA, USA) was used for blocking, the primary antibody reaction, the secondary antibody reaction, and the binding of avidin to the biotin complex.

Immunohistochemical staining:

Article Title: The Molecular Pathogenesis of Tumor-Suppressive miR-486-5p and miR-486-3p Target Genes: GINS4 Facilitates Aggressiveness in Lung Adenocarcinoma
Article Snippet: .. GINS4 expression was evaluated by immunohistochemical staining using tissue microarray slides (catalog no.: LC811a, US Biomax, Inc. Derwood, MD, USA). .. The VECTASTAIN Universal Elite ABC Kit (catalog no.: PK-6200, Vector Laboratories, Burlingame, CA, USA) was used for blocking, the primary antibody reaction, the secondary antibody reaction, and the binding of avidin to the biotin complex.

Article Title: Minichromosome maintenance proteins in lung adenocarcinoma: Clinical significance and therapeutic targets.
Article Snippet: .. Tissue microarray slides (catalog no.: LC811a; US Biomax, Inc., Derwood, MD, USA) were used for immunohistochemical staining. .. Blocking, the primary antibody reaction, secondary antibody reaction, and binding of avidin to the biotin complex were conducted using a VECTASTAIN Universal Elite ABC Kit (Vector Laboratories, Burlingame, CA, USA) according to the manufacturer’s protocol.

Staining:

Article Title: The Molecular Pathogenesis of Tumor-Suppressive miR-486-5p and miR-486-3p Target Genes: GINS4 Facilitates Aggressiveness in Lung Adenocarcinoma
Article Snippet: .. GINS4 expression was evaluated by immunohistochemical staining using tissue microarray slides (catalog no.: LC811a, US Biomax, Inc. Derwood, MD, USA). .. The VECTASTAIN Universal Elite ABC Kit (catalog no.: PK-6200, Vector Laboratories, Burlingame, CA, USA) was used for blocking, the primary antibody reaction, the secondary antibody reaction, and the binding of avidin to the biotin complex.

Article Title: Minichromosome maintenance proteins in lung adenocarcinoma: Clinical significance and therapeutic targets.
Article Snippet: .. Tissue microarray slides (catalog no.: LC811a; US Biomax, Inc., Derwood, MD, USA) were used for immunohistochemical staining. .. Blocking, the primary antibody reaction, secondary antibody reaction, and binding of avidin to the biotin complex were conducted using a VECTASTAIN Universal Elite ABC Kit (Vector Laboratories, Burlingame, CA, USA) according to the manufacturer’s protocol.



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Upregulation of MHC class II antigen in human melanoma xenografts treated systemically with anle138b, and expression of α-synuclein, MHC class II, and MHC class I proteins in melanoma <t>TMA</t> cores. (a) A tissue section from a nontreated WM983-B tumor xenograft probed with an antibody to human MHC class II (HLA-DPB1) protein (pseudocolored green). (b) A tissue section from an anle138b-treated WM983-B tumor xenograft probed with an antibody to human MHC class II (HLA-DPB1) protein (pseudocolored green). (c) Fluorescence intensity level of expression of proteins – α-synuclein (pseudocolored red), MHC II (pseudocolored yellow), MHC I (pseudocolored green) – in areas, encircled by a white line, in tissue sections from three of the Stage II and from one of the Stage IV melanoma TMA cores in which α-synuclein or vice versa, MHC II, or MHC I protein was expressed more strongly. TMA, tissue <t>microarray.</t>
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Upregulation of MHC class II antigen in human melanoma xenografts treated systemically with anle138b, and expression of α-synuclein, MHC class II, and MHC class I proteins in melanoma <t>TMA</t> cores. (a) A tissue section from a nontreated WM983-B tumor xenograft probed with an antibody to human MHC class II (HLA-DPB1) protein (pseudocolored green). (b) A tissue section from an anle138b-treated WM983-B tumor xenograft probed with an antibody to human MHC class II (HLA-DPB1) protein (pseudocolored green). (c) Fluorescence intensity level of expression of proteins – α-synuclein (pseudocolored red), MHC II (pseudocolored yellow), MHC I (pseudocolored green) – in areas, encircled by a white line, in tissue sections from three of the Stage II and from one of the Stage IV melanoma TMA cores in which α-synuclein or vice versa, MHC II, or MHC I protein was expressed more strongly. TMA, tissue <t>microarray.</t>
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(A) Melanoma cell lines were transiently transfected with an EGFP-LC3 expressing plasmid and grown in normal medium. 24 hours after transfection, the cells were fixed and the autophagosomes in the cells were visualized by the presence of LC3 puncta under fluorescence microscopy, with the percentages of cells showing LC3 puncta (mean ± SD) indicated. All tested cell lines showed positive punctation indicating high basal autophagy. (B) Western blot shows that melanoma cell lines have high basal LC3-II and p62 protein levels. Upon HBSS induced starvation, increased cleavage of LC3-I to LC3-II indicative of autophagy induction and decreased or unchanged p62 levels were seen. Extracts from autophagy competent and autophagy deficient iBMK cells served as positive and negative controls. (C) Immunofluorescence staining for endogenous LC3 on a human melanoma tissue <t>microarray.</t> Punctate LC3 localization for autophagosomes is indicated by red arrows (top panel). The percentages of specimens with punctate LC3 staining in malignant, metastatic and benign nevus groups are indicated in the table (bottom panel). (D) Western blot showed decreased expression levels of Atg7 (top panel) and impaired clonogenic survival (bottom panel) in response to lentiviral shRNA knockdown of the essential autophagy regulator Atg7.
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Biomax Inc melanoma tissue microarray analysis (tma) slides
The consistency of YAP and LRP1 in tissue <t>microarray</t> specimen. ( a , b ) <t>TMA</t> slides include forty skin melanoma tissues and eight skin normal tissues which locate on the bottom of the each TMA. Representative images of IHC from HCC TMA stained with anti-YAP or anti-LRP1 antibodies. Scale bar, 100 μM. ( c ) Representative images of IHC from skin melanoma HCC TMA stained with anti-YAP or anti-LRP1 antibodies. Scale bar, 100 μM. ( d ) The statistical figure of skin melanoma IHC images from HCC TMA stained with anti-YAP or anti-LRP1 antibodies. The TMA data were analyzed using the χ2 test.
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Image Search Results


Upregulation of MHC class II antigen in human melanoma xenografts treated systemically with anle138b, and expression of α-synuclein, MHC class II, and MHC class I proteins in melanoma TMA cores. (a) A tissue section from a nontreated WM983-B tumor xenograft probed with an antibody to human MHC class II (HLA-DPB1) protein (pseudocolored green). (b) A tissue section from an anle138b-treated WM983-B tumor xenograft probed with an antibody to human MHC class II (HLA-DPB1) protein (pseudocolored green). (c) Fluorescence intensity level of expression of proteins – α-synuclein (pseudocolored red), MHC II (pseudocolored yellow), MHC I (pseudocolored green) – in areas, encircled by a white line, in tissue sections from three of the Stage II and from one of the Stage IV melanoma TMA cores in which α-synuclein or vice versa, MHC II, or MHC I protein was expressed more strongly. TMA, tissue microarray.

Journal: Melanoma Research

Article Title: Interfering with aggregated α-synuclein in advanced melanoma leads to a major upregulation of MHC class II proteins

doi: 10.1097/CMR.0000000000000982

Figure Lengend Snippet: Upregulation of MHC class II antigen in human melanoma xenografts treated systemically with anle138b, and expression of α-synuclein, MHC class II, and MHC class I proteins in melanoma TMA cores. (a) A tissue section from a nontreated WM983-B tumor xenograft probed with an antibody to human MHC class II (HLA-DPB1) protein (pseudocolored green). (b) A tissue section from an anle138b-treated WM983-B tumor xenograft probed with an antibody to human MHC class II (HLA-DPB1) protein (pseudocolored green). (c) Fluorescence intensity level of expression of proteins – α-synuclein (pseudocolored red), MHC II (pseudocolored yellow), MHC I (pseudocolored green) – in areas, encircled by a white line, in tissue sections from three of the Stage II and from one of the Stage IV melanoma TMA cores in which α-synuclein or vice versa, MHC II, or MHC I protein was expressed more strongly. TMA, tissue microarray.

Article Snippet: Four melanoma tissue microarray (TMA) slides ( https://www.biomax.us/tissue-arrays/Melanoma/ME811 ), each containing two tissue sections from the same 39 cases of melanoma, and tissue sections from three cases of normal skin tissue were heated at 60 °C, deparaffinized and rehydrated.

Techniques: Expressing, Fluorescence, Microarray

(A) Melanoma cell lines were transiently transfected with an EGFP-LC3 expressing plasmid and grown in normal medium. 24 hours after transfection, the cells were fixed and the autophagosomes in the cells were visualized by the presence of LC3 puncta under fluorescence microscopy, with the percentages of cells showing LC3 puncta (mean ± SD) indicated. All tested cell lines showed positive punctation indicating high basal autophagy. (B) Western blot shows that melanoma cell lines have high basal LC3-II and p62 protein levels. Upon HBSS induced starvation, increased cleavage of LC3-I to LC3-II indicative of autophagy induction and decreased or unchanged p62 levels were seen. Extracts from autophagy competent and autophagy deficient iBMK cells served as positive and negative controls. (C) Immunofluorescence staining for endogenous LC3 on a human melanoma tissue microarray. Punctate LC3 localization for autophagosomes is indicated by red arrows (top panel). The percentages of specimens with punctate LC3 staining in malignant, metastatic and benign nevus groups are indicated in the table (bottom panel). (D) Western blot showed decreased expression levels of Atg7 (top panel) and impaired clonogenic survival (bottom panel) in response to lentiviral shRNA knockdown of the essential autophagy regulator Atg7.

Journal: PLoS ONE

Article Title: Coordinate Autophagy and mTOR Pathway Inhibition Enhances Cell Death in Melanoma

doi: 10.1371/journal.pone.0055096

Figure Lengend Snippet: (A) Melanoma cell lines were transiently transfected with an EGFP-LC3 expressing plasmid and grown in normal medium. 24 hours after transfection, the cells were fixed and the autophagosomes in the cells were visualized by the presence of LC3 puncta under fluorescence microscopy, with the percentages of cells showing LC3 puncta (mean ± SD) indicated. All tested cell lines showed positive punctation indicating high basal autophagy. (B) Western blot shows that melanoma cell lines have high basal LC3-II and p62 protein levels. Upon HBSS induced starvation, increased cleavage of LC3-I to LC3-II indicative of autophagy induction and decreased or unchanged p62 levels were seen. Extracts from autophagy competent and autophagy deficient iBMK cells served as positive and negative controls. (C) Immunofluorescence staining for endogenous LC3 on a human melanoma tissue microarray. Punctate LC3 localization for autophagosomes is indicated by red arrows (top panel). The percentages of specimens with punctate LC3 staining in malignant, metastatic and benign nevus groups are indicated in the table (bottom panel). (D) Western blot showed decreased expression levels of Atg7 (top panel) and impaired clonogenic survival (bottom panel) in response to lentiviral shRNA knockdown of the essential autophagy regulator Atg7.

Article Snippet: Human Malignant Melanoma Tissue Microarray (US Biomax, Inc) slides, or xenograft tumor paraffin slides were deparaffinized, hydrated and incubated with primary antibody against LC3 (Nanotools, 1∶100 dilution) for 15 min at room temperature followed by FITC tagged anti-mouse (Jackson Immuno Research) antibody, then mounted and visualized by epifluorescence microscopy.

Techniques: Transfection, Expressing, Plasmid Preparation, Fluorescence, Microscopy, Western Blot, Immunofluorescence, Staining, Microarray, shRNA

The consistency of YAP and LRP1 in tissue microarray specimen. ( a , b ) TMA slides include forty skin melanoma tissues and eight skin normal tissues which locate on the bottom of the each TMA. Representative images of IHC from HCC TMA stained with anti-YAP or anti-LRP1 antibodies. Scale bar, 100 μM. ( c ) Representative images of IHC from skin melanoma HCC TMA stained with anti-YAP or anti-LRP1 antibodies. Scale bar, 100 μM. ( d ) The statistical figure of skin melanoma IHC images from HCC TMA stained with anti-YAP or anti-LRP1 antibodies. The TMA data were analyzed using the χ2 test.

Journal: Scientific Reports

Article Title: Yes-Associated Protein (YAP) Promotes Tumorigenesis in Melanoma Cells Through Stimulation of Low-Density Lipoprotein Receptor-Related Protein 1 (LRP1)

doi: 10.1038/s41598-017-14764-4

Figure Lengend Snippet: The consistency of YAP and LRP1 in tissue microarray specimen. ( a , b ) TMA slides include forty skin melanoma tissues and eight skin normal tissues which locate on the bottom of the each TMA. Representative images of IHC from HCC TMA stained with anti-YAP or anti-LRP1 antibodies. Scale bar, 100 μM. ( c ) Representative images of IHC from skin melanoma HCC TMA stained with anti-YAP or anti-LRP1 antibodies. Scale bar, 100 μM. ( d ) The statistical figure of skin melanoma IHC images from HCC TMA stained with anti-YAP or anti-LRP1 antibodies. The TMA data were analyzed using the χ2 test.

Article Snippet: For IHC, melanoma tissue microarray analysis (TMA) slides were purchased from Biomax (Rockville, MD, USA).

Techniques: Microarray, Staining