human tissue expression data Search Results


human tissue samples and associated data  (ProPath Laboratory Inc)
90
ProPath Laboratory Inc human tissue samples and associated data
Human Tissue Samples And Associated Data, supplied by ProPath Laboratory 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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human tissue samples and associated data - by Bioz Stars, 2026-07
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rna-seq data human and mouse tissues  (Epigenomics ag)
90
Epigenomics ag rna-seq data human and mouse tissues
Rna Seq Data Human And Mouse Tissues, supplied by Epigenomics ag, 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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rna-seq data human and mouse tissues - by Bioz Stars, 2026-07
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tnm stage data  (Cooperative Human Tissue Network (CHTN)
90
Cooperative Human Tissue Network (CHTN tnm stage data
Tnm Stage Data, supplied by Cooperative Human Tissue Network (CHTN, 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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tnm stage data - by Bioz Stars, 2026-07
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expression profiles for 10 selected proteins in 33 normal human tissues  (Pantomics Inc)
90
Pantomics Inc expression profiles for 10 selected proteins in 33 normal human tissues
Expression Profiles For 10 Selected Proteins In 33 Normal Human Tissues, supplied by Pantomics 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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expression profiles for 10 selected proteins in 33 normal human tissues - by Bioz Stars, 2026-07
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blm expression  (Cooperative Human Tissue Network (CHTN)
90
Cooperative Human Tissue Network (CHTN blm expression
Blm Expression, supplied by Cooperative Human Tissue Network (CHTN, 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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blm expression - by Bioz Stars, 2026-07
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human rna multiple tissue expression array  (Becton Dickinson)
90
Becton Dickinson human rna multiple tissue expression array
Human Rna Multiple Tissue Expression Array, supplied by Becton Dickinson, 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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human rna multiple tissue expression array - by Bioz Stars, 2026-07
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gene expression across 57 human tissues  (Epigenomics ag)
90
Epigenomics ag gene expression across 57 human tissues
Gene Expression Across 57 Human Tissues, supplied by Epigenomics ag, 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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gene expression across 57 human tissues - by Bioz Stars, 2026-07
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prlr isoform expression  (Cooperative Human Tissue Network (CHTN)
90
Cooperative Human Tissue Network (CHTN prlr isoform expression
Characterization of <t>PRLR</t> <t>isoform</t> antibodies. A. Western blot analysis indicating specificity of polyclonal antibodies. CHO cells were transiently transfected with isoform specific PRLR cDNA as described. Cell lysates were prepared and proteins separated by PAGE. Each isoform specific lysate was probed with each isoform specific antibody. Each transfection was performed in triplicate and Western blot analysis performed twice. Data shown are a representative autoradiogram. Molecular weights are marked as indicated: LF = 93 kDa, SF1a = 57 kDa, SF1b = 38 kDa. Cell lysates from CHO transfected cells were immunoprecipitated with their respective antibodies, then immunoblotted with the same antibodies. Each transfection was performed in triplicate and Western blot analysis performed twice. Data shown are a representative autoradiogram. IP indicates immunoprecipitation. B. Western blot analysis using commercially available PRLR antibody. ECD = antibody recognizing extracellular domain C. Fluorescent immunocytochemical analysis. CHO cells were transiently transfected with isoform specific PRLR cDNA as described. Specific staining was observed using isoform specific polyclonal antibodies. The negative control (not shown) lacks primary antibody and appears black. Data shown are representative of triplicate experiments. Magnification 20×.
Prlr Isoform Expression, supplied by Cooperative Human Tissue Network (CHTN, 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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prlr isoform expression - by Bioz Stars, 2026-07
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human white adipose tissue single-cell rna sequencing data  (Broad Institute Inc)
90
Broad Institute Inc human white adipose tissue single-cell rna sequencing data
Characterization of <t>PRLR</t> <t>isoform</t> antibodies. A. Western blot analysis indicating specificity of polyclonal antibodies. CHO cells were transiently transfected with isoform specific PRLR cDNA as described. Cell lysates were prepared and proteins separated by PAGE. Each isoform specific lysate was probed with each isoform specific antibody. Each transfection was performed in triplicate and Western blot analysis performed twice. Data shown are a representative autoradiogram. Molecular weights are marked as indicated: LF = 93 kDa, SF1a = 57 kDa, SF1b = 38 kDa. Cell lysates from CHO transfected cells were immunoprecipitated with their respective antibodies, then immunoblotted with the same antibodies. Each transfection was performed in triplicate and Western blot analysis performed twice. Data shown are a representative autoradiogram. IP indicates immunoprecipitation. B. Western blot analysis using commercially available PRLR antibody. ECD = antibody recognizing extracellular domain C. Fluorescent immunocytochemical analysis. CHO cells were transiently transfected with isoform specific PRLR cDNA as described. Specific staining was observed using isoform specific polyclonal antibodies. The negative control (not shown) lacks primary antibody and appears black. Data shown are representative of triplicate experiments. Magnification 20×.
Human White Adipose Tissue Single Cell Rna Sequencing Data, supplied by Broad 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
https://www.bioz.com/product/human+tissue+expression+data/pmc11960805-552-0-17?v=Broad+Institute+Inc
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human white adipose tissue single-cell rna sequencing data - by Bioz Stars, 2026-07
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recq expression level  (Cooperative Human Tissue Network (CHTN)
90
Cooperative Human Tissue Network (CHTN recq expression level
Characterization of <t>PRLR</t> <t>isoform</t> antibodies. A. Western blot analysis indicating specificity of polyclonal antibodies. CHO cells were transiently transfected with isoform specific PRLR cDNA as described. Cell lysates were prepared and proteins separated by PAGE. Each isoform specific lysate was probed with each isoform specific antibody. Each transfection was performed in triplicate and Western blot analysis performed twice. Data shown are a representative autoradiogram. Molecular weights are marked as indicated: LF = 93 kDa, SF1a = 57 kDa, SF1b = 38 kDa. Cell lysates from CHO transfected cells were immunoprecipitated with their respective antibodies, then immunoblotted with the same antibodies. Each transfection was performed in triplicate and Western blot analysis performed twice. Data shown are a representative autoradiogram. IP indicates immunoprecipitation. B. Western blot analysis using commercially available PRLR antibody. ECD = antibody recognizing extracellular domain C. Fluorescent immunocytochemical analysis. CHO cells were transiently transfected with isoform specific PRLR cDNA as described. Specific staining was observed using isoform specific polyclonal antibodies. The negative control (not shown) lacks primary antibody and appears black. Data shown are representative of triplicate experiments. Magnification 20×.
Recq Expression Level, supplied by Cooperative Human Tissue Network (CHTN, 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/human+tissue+expression+data/pmc03730021-188-2-12?v=Cooperative+Human+Tissue+Network+%28CHTN
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recq expression level - by Bioz Stars, 2026-07
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super-express mrna β-actin-normalized northern blot of 12 human normal adult tissues nmhan-vii-e  (BioChain Institute)
90
BioChain Institute super-express mrna β-actin-normalized northern blot of 12 human normal adult tissues nmhan-vii-e
Characterization of <t>PRLR</t> <t>isoform</t> antibodies. A. Western blot analysis indicating specificity of polyclonal antibodies. CHO cells were transiently transfected with isoform specific PRLR cDNA as described. Cell lysates were prepared and proteins separated by PAGE. Each isoform specific lysate was probed with each isoform specific antibody. Each transfection was performed in triplicate and Western blot analysis performed twice. Data shown are a representative autoradiogram. Molecular weights are marked as indicated: LF = 93 kDa, SF1a = 57 kDa, SF1b = 38 kDa. Cell lysates from CHO transfected cells were immunoprecipitated with their respective antibodies, then immunoblotted with the same antibodies. Each transfection was performed in triplicate and Western blot analysis performed twice. Data shown are a representative autoradiogram. IP indicates immunoprecipitation. B. Western blot analysis using commercially available PRLR antibody. ECD = antibody recognizing extracellular domain C. Fluorescent immunocytochemical analysis. CHO cells were transiently transfected with isoform specific PRLR cDNA as described. Specific staining was observed using isoform specific polyclonal antibodies. The negative control (not shown) lacks primary antibody and appears black. Data shown are representative of triplicate experiments. Magnification 20×.
Super Express Mrna β Actin Normalized Northern Blot Of 12 Human Normal Adult Tissues Nmhan Vii E, supplied by BioChain Institute, 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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super-express mrna β-actin-normalized northern blot of 12 human normal adult tissues nmhan-vii-e - by Bioz Stars, 2026-07
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version 22 0  (Human Protein Atlas)
86
Human Protein Atlas version 22 0
Characterization of <t>PRLR</t> <t>isoform</t> antibodies. A. Western blot analysis indicating specificity of polyclonal antibodies. CHO cells were transiently transfected with isoform specific PRLR cDNA as described. Cell lysates were prepared and proteins separated by PAGE. Each isoform specific lysate was probed with each isoform specific antibody. Each transfection was performed in triplicate and Western blot analysis performed twice. Data shown are a representative autoradiogram. Molecular weights are marked as indicated: LF = 93 kDa, SF1a = 57 kDa, SF1b = 38 kDa. Cell lysates from CHO transfected cells were immunoprecipitated with their respective antibodies, then immunoblotted with the same antibodies. Each transfection was performed in triplicate and Western blot analysis performed twice. Data shown are a representative autoradiogram. IP indicates immunoprecipitation. B. Western blot analysis using commercially available PRLR antibody. ECD = antibody recognizing extracellular domain C. Fluorescent immunocytochemical analysis. CHO cells were transiently transfected with isoform specific PRLR cDNA as described. Specific staining was observed using isoform specific polyclonal antibodies. The negative control (not shown) lacks primary antibody and appears black. Data shown are representative of triplicate experiments. Magnification 20×.
Version 22 0, supplied by Human Protein Atlas, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/human+tissue+expression+data/pmc12335587-95-12-9?v=Human+Protein+Atlas
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version 22 0 - by Bioz Stars, 2026-07
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Image Search Results


Characterization of PRLR isoform antibodies. A. Western blot analysis indicating specificity of polyclonal antibodies. CHO cells were transiently transfected with isoform specific PRLR cDNA as described. Cell lysates were prepared and proteins separated by PAGE. Each isoform specific lysate was probed with each isoform specific antibody. Each transfection was performed in triplicate and Western blot analysis performed twice. Data shown are a representative autoradiogram. Molecular weights are marked as indicated: LF = 93 kDa, SF1a = 57 kDa, SF1b = 38 kDa. Cell lysates from CHO transfected cells were immunoprecipitated with their respective antibodies, then immunoblotted with the same antibodies. Each transfection was performed in triplicate and Western blot analysis performed twice. Data shown are a representative autoradiogram. IP indicates immunoprecipitation. B. Western blot analysis using commercially available PRLR antibody. ECD = antibody recognizing extracellular domain C. Fluorescent immunocytochemical analysis. CHO cells were transiently transfected with isoform specific PRLR cDNA as described. Specific staining was observed using isoform specific polyclonal antibodies. The negative control (not shown) lacks primary antibody and appears black. Data shown are representative of triplicate experiments. Magnification 20×.

Journal: BMC Cancer

Article Title: Characterization of ductal and lobular breast carcinomas using novel prolactin receptor isoform specific antibodies

doi: 10.1186/1471-2407-10-678

Figure Lengend Snippet: Characterization of PRLR isoform antibodies. A. Western blot analysis indicating specificity of polyclonal antibodies. CHO cells were transiently transfected with isoform specific PRLR cDNA as described. Cell lysates were prepared and proteins separated by PAGE. Each isoform specific lysate was probed with each isoform specific antibody. Each transfection was performed in triplicate and Western blot analysis performed twice. Data shown are a representative autoradiogram. Molecular weights are marked as indicated: LF = 93 kDa, SF1a = 57 kDa, SF1b = 38 kDa. Cell lysates from CHO transfected cells were immunoprecipitated with their respective antibodies, then immunoblotted with the same antibodies. Each transfection was performed in triplicate and Western blot analysis performed twice. Data shown are a representative autoradiogram. IP indicates immunoprecipitation. B. Western blot analysis using commercially available PRLR antibody. ECD = antibody recognizing extracellular domain C. Fluorescent immunocytochemical analysis. CHO cells were transiently transfected with isoform specific PRLR cDNA as described. Specific staining was observed using isoform specific polyclonal antibodies. The negative control (not shown) lacks primary antibody and appears black. Data shown are representative of triplicate experiments. Magnification 20×.

Article Snippet: PRLR isoform expression was examined on 12 lobular carcinoma and 10 ductal carcinoma specimens obtained from CHTN; other investigators may have received samples from these same tissues.

Techniques: Western Blot, Transfection, Immunoprecipitation, Staining, Negative Control

Immunoanalysis on human xenografts. A. Fluorescent immunohistochemistry was performed on MCF7, MDA-MB-231, or T47D cells which were injected into the cleared fat pads of nude mice; once tumors reached 1 cm 2 (measured in two dimensions), they were excised, formalin fixed, sectioned, and stained with the indicated PRLR isoform specific antibodies. B. Immunohistochemical analysis using DAB as chromogen of MCF7, MDA-MB-231, or T47D xenograft tumors. neg = no primary antibody as negative control; DAPI stain to visualize the presence of cells. Photographs are representative from 5 different tumors for each cell line. Magnification 40×.

Journal: BMC Cancer

Article Title: Characterization of ductal and lobular breast carcinomas using novel prolactin receptor isoform specific antibodies

doi: 10.1186/1471-2407-10-678

Figure Lengend Snippet: Immunoanalysis on human xenografts. A. Fluorescent immunohistochemistry was performed on MCF7, MDA-MB-231, or T47D cells which were injected into the cleared fat pads of nude mice; once tumors reached 1 cm 2 (measured in two dimensions), they were excised, formalin fixed, sectioned, and stained with the indicated PRLR isoform specific antibodies. B. Immunohistochemical analysis using DAB as chromogen of MCF7, MDA-MB-231, or T47D xenograft tumors. neg = no primary antibody as negative control; DAPI stain to visualize the presence of cells. Photographs are representative from 5 different tumors for each cell line. Magnification 40×.

Article Snippet: PRLR isoform expression was examined on 12 lobular carcinoma and 10 ductal carcinoma specimens obtained from CHTN; other investigators may have received samples from these same tissues.

Techniques: Immunohistochemistry, Injection, Staining, Immunohistochemical staining, Negative Control

Message for PRLR isoforms in breast carcinomas. RNA was extracted from 7 ductal (left) and 7 lobular (right) carcinomas and qPCR was performed. Data shown are the mean +/- SE of delta delta Ct values relative to SF1a expression.

Journal: BMC Cancer

Article Title: Characterization of ductal and lobular breast carcinomas using novel prolactin receptor isoform specific antibodies

doi: 10.1186/1471-2407-10-678

Figure Lengend Snippet: Message for PRLR isoforms in breast carcinomas. RNA was extracted from 7 ductal (left) and 7 lobular (right) carcinomas and qPCR was performed. Data shown are the mean +/- SE of delta delta Ct values relative to SF1a expression.

Article Snippet: PRLR isoform expression was examined on 12 lobular carcinoma and 10 ductal carcinoma specimens obtained from CHTN; other investigators may have received samples from these same tissues.

Techniques: Expressing

Immunohistochemical analysis from ductal breast tissue arrays. Representative photographs taken of ductal carcinoma specimens to demonstrate absent, low, medium, or high amounts of fluorescent red intensity staining. 144 individual ductal specimens were stained with PRLR isoform specific antibodies and analyzed. Scale bar indicates range of red scoring.

Journal: BMC Cancer

Article Title: Characterization of ductal and lobular breast carcinomas using novel prolactin receptor isoform specific antibodies

doi: 10.1186/1471-2407-10-678

Figure Lengend Snippet: Immunohistochemical analysis from ductal breast tissue arrays. Representative photographs taken of ductal carcinoma specimens to demonstrate absent, low, medium, or high amounts of fluorescent red intensity staining. 144 individual ductal specimens were stained with PRLR isoform specific antibodies and analyzed. Scale bar indicates range of red scoring.

Article Snippet: PRLR isoform expression was examined on 12 lobular carcinoma and 10 ductal carcinoma specimens obtained from CHTN; other investigators may have received samples from these same tissues.

Techniques: Immunohistochemical staining, Staining

Immunohistochemical analysis from lobular breast tissue arrays. Representative photographs of lobular carcinoma specimens to demonstrate absent, low, medium, or high amounts of fluorescent red intensity staining. 104 individual lobular specimens were stained with PRLR isoform specific antibodies and analyzed. Scale bar indicates range of red scoring.

Journal: BMC Cancer

Article Title: Characterization of ductal and lobular breast carcinomas using novel prolactin receptor isoform specific antibodies

doi: 10.1186/1471-2407-10-678

Figure Lengend Snippet: Immunohistochemical analysis from lobular breast tissue arrays. Representative photographs of lobular carcinoma specimens to demonstrate absent, low, medium, or high amounts of fluorescent red intensity staining. 104 individual lobular specimens were stained with PRLR isoform specific antibodies and analyzed. Scale bar indicates range of red scoring.

Article Snippet: PRLR isoform expression was examined on 12 lobular carcinoma and 10 ductal carcinoma specimens obtained from CHTN; other investigators may have received samples from these same tissues.

Techniques: Immunohistochemical staining, Staining