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Recombinant Mouse Antibodies

Home >> Antibodies >> Recombinant Mouse Antibodies

Recombinant Mouse Antibodies

Found all antibodies, displaying 611 to 619
DSG1 Antibody / Desmoglein 1 (clone MSVA-544M)
Catalog No : V6068
Applications : IHC
Reactivity : Human
Format : Purified
Recmousemono
Immunohistochemistry of DSG1 Antibody for IHC in normal and cancer tissue microarrays. Formalin-fixed, paraffin-embedded human tissue microarrays were stained with recombinant Desmoglein-1 mouse monoclonal antibody clone MSVA-544M. In normal tissues, strong membranous staining is observed in stratified squamous epithelium including skin, esophagus, and tonsil surface epithelium, consistent with Desmoglein 1 localization in suprabasal keratinocytes. Most non-stratified epithelia and non-epithelial tissues show little to no staining.<BR>In the cancer tissue panel, membranous staining is present in squamous cell carcinomas, including larynx, oral cavity, vulva, and cervix, as well as in selected urothelial carcinomas, consistent with retained epithelial differentiation. Most adenocarcinomas and non-epithelial malignancies demonstrate minimal or negative staining.<BR>The observed tissue distribution and tumor staining profile align with established Desmoglein 1 expression patterns reported in the Human Protein Atlas, supporting the specificity of clone MSVA-544M for desmosomal epithelial cell-cell junctions.
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IBA1 Antibody / AIF1 / Allograft inflammatory factor 1 (clone MSVA-955M)
Catalog No : V6070
Applications : IHC
Reactivity : Human
Format : Purified
Recmousemono
Immunohistochemistry of AIF1 Antibody for IHC in human tissue microarrays. Formalin-fixed, paraffin-embedded normal and cancer tissue microarrays demonstrate cytoplasmic HRP-DAB brown staining in macrophages, monocytes, and microglia-rich tissues, while epithelial and stromal cells are largely negative. Staining was performed using clone MSVA-955M. Strong immunoreactivity is observed in spleen, lymph node, tonsil, and inflammatory cell infiltrates across multiple tumor types, consistent with expected Allograft inflammatory factor 1 / IBA1 expression patterns reported in the Human Protein Atlas.
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FABP1 Antibody / Fatty acid-binding protein 1 (clone MSVA-501M)
Catalog No : V6073
Applications : IHC
Reactivity : Human
Format : Purified
Recmousemono
Immunohistochemistry of FABP1 Antibody for IHC (clone MSVA-501M) in human tissue microarrays. FFPE human normal and cancer tissues were stained with FABP1 antibody for IHC (clone MSVA-501M). In the normal tissue gallery, strong cytoplasmic HRP-DAB brown staining is observed in hepatocytes of liver, consistent with the known high expression of Liver fatty acid binding protein. Prominent cytoplasmic staining is also seen in small intestinal enterocytes and renal proximal tubular epithelial cells, while most other tissues show low to absent staining. In the cancer tissue gallery, hepatocellular carcinoma demonstrates retained cytoplasmic FABP1 expression, whereas many non-hepatic tumors show minimal or negative staining, consistent with reported expression patterns in Human Protein Atlas. The overall staining distribution supports the expected tissue-specific expression profile of FABP1.
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CELA3B Antibody / Chymotrypsin like elastase 3B (clone MSVA-410M)
Catalog No : V6076
Applications : IHC
Reactivity : Human
Format : Purified
Recmousemono
Immunohistochemistry of CELA3B Antibody for IHC in human tissue microarrays. Formalin-fixed, paraffin-embedded normal and cancer tissues were stained using the recombinant mouse monoclonal clone MSVA-410M. Strong cytoplasmic staining is observed in normal pancreatic acinar cells, consistent with the known secretory localization of Chymotrypsin-like elastase family member 3B, while the majority of non-pancreatic tissues are negative. In the cancer panel, pancreatic acinar cell carcinoma shows strong cytoplasmic positivity, whereas most other tumor types are negative, supporting lineage-associated expression. Staining patterns align with published expression data in the Human Protein Atlas.
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GAD65 Antibody / Glutamate decarboxylase 2 (clone MSVA-602M)
Catalog No : V6079
Applications : IHC
Reactivity : Human
Format : Purified
Recmousemono
Immunohistochemistry of GAD2 Antibody for IHC (clone MSVA-602M) in human tissue microarrays. Formalin-fixed, paraffin-embedded normal and cancer tissues demonstrate selective cytoplasmic staining in neuronal-rich regions of brain tissue, consistent with GABAergic neuron localization of Glutamate decarboxylase 2 / GAD65. Non-neuronal tissues show minimal staining, while tumor samples largely lack significant signal except in rare neuroendocrine or neuronal-derived contexts. The observed distribution pattern across normal and malignant tissues aligns with publicly available expression data from the Human Protein Atlas.
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Glycoprotein 2 Antibody / GP2 / ZAP75 (clone MSVA-475M)
Catalog No : V6081
Applications : IHC
Reactivity : Human
Format : Purified
Recmousemono
Immunohistochemistry analysis of Glycoprotein 2 antibody in human tissue microarrays. Formalin-fixed, paraffin-embedded human tissue microarrays containing multiple normal and cancer tissues were stained using GP2 Antibody for IHC recognizing Glycoprotein 2 (clone MSVA-475M). Strong HRP-DAB brown staining is observed in pancreatic acinar cells, consistent with the known localization of pancreatic secretory granule membrane major glycoprotein GP2 within zymogen granules. Most other normal tissues show little to no detectable staining. In cancer tissues, strong cytoplasmic staining is observed in pancreatic acinar cell carcinoma, while most other tumor types remain negative, supporting the tissue-restricted expression pattern of Glycoprotein 2. The staining distribution observed across these tissues aligns with expression patterns reported in the Human Protein Atlas.
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MPO Antibody / Myeloperoxidase (clone MSVA-692M)
Catalog No : V6098
Applications : IHC
Reactivity : Human
Format : Purified
Recmousemono
Myeloperoxidase Antibody for IHC / MPO Immunohistochemistry Antibody (clone MSVA-692M). Immunohistochemistry analysis of FFPE human tissue microarrays using Myeloperoxidase antibody for IHC (clone MSVA-692M). Strong cytoplasmic brown staining is observed in granulocytic cells within bone marrow and scattered inflammatory cells in tissues such as tonsil and spleen, consistent with the known localization of Myeloperoxidase / MPO in neutrophil lineage cells. Most epithelial and stromal tissues show minimal staining. The observed immunohistochemistry staining patterns across normal and cancer tissues align with MPO expression profiles reported in the Human Protein Atlas.
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PAX6 Antibody / Paired box protein Pax-6 (clone MSVA-706M)
Catalog No : V6102
Applications : IHC
Reactivity : Human
Format : Purified
Recmousemono
PAX6 Antibody for IHC immunohistochemistry analysis of human tissue microarrays. PAX6 Antibody for IHC (clone MSVA-706M) was tested on a wide panel of normal and cancer tissues. Nuclear HRP-DAB chromogenic staining identifies Pax-6 expressing cells, with strongest signal observed in pancreatic endocrine cells within islets. The immunohistochemistry staining patterns across tissues are consistent with expression data reported in the Human Protein Atlas.
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ACP3 Antibody / Prostatic acid phosphatase (clone MSVA-452M)
Catalog No : V6105
Applications : IHC
Reactivity : Human
Format : Purified
Recmousemono
Prostatic Acid Phosphatase Antibody for IHC / PAP Antibody (ACP3) (clone MSVA-452M) tissue microarray immunohistochemistry analysis of Prostatic acid phosphatase / ACP3. FFPE human normal and cancer tissue microarrays were stained with the recombinant mouse monoclonal Prostatic Acid Phosphatase Antibody for IHC (clone MSVA-452M). HRP-DAB brown chromogenic signal is observed in prostate glandular epithelial cells and prostate adenocarcinoma, consistent with the known prostate-restricted expression of Prostatic acid phosphatase (PAP/ACP3). Other normal tissues and non-prostate tumor samples show little to no staining. Prostatic acid phosphatase immunohistochemistry is commonly used in prostate cancer research to identify prostate epithelial differentiation and evaluate PAP expression in prostate tumors.
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