YTHDC1 Antibody / Nuclear m6A Reader Protein Antibody (RQ6218)

YTHDC1 Antibody Human Colon Cancer IHC. Immunohistochemical analysis of YTHDC1 Antibody / Nuclear m6A Reader Protein Antibody in FFPE human colon cancer tissue. Following heat-induced epitope retrieval in pH 8.0 EDTA buffer, sections were stained with YTHDC1 antibody at 2 ug/ml and detected using an HRP-conjugated secondary antibody with DAB chromogen. Predominantly nuclear staining is observed in the malignant epithelial cells, consistent with the nuclear localization of YTHDC1 and its role as an m6A RNA reader that regulates RNA processing and gene expression. This YTHDC1 Antibody, a Nuclear m6A Reader Protein Antibody, is well suited for studies of epitranscriptomic regulation and YTHDC1 expression in cancer tissues.

YTHDC1 Antibody Human Colon Adenocarcinoma IHC. Immunohistochemical analysis of YTHDC1 Antibody / Nuclear m6A Reader Protein Antibody in FFPE human colon adenocarcinoma tissue. Following heat-induced epitope retrieval in pH 8.0 EDTA buffer, sections were stained with YTHDC1 antibody at 2 ug/ml and detected using an HRP-conjugated secondary antibody with DAB chromogen. Distinct nuclear staining is observed in the neoplastic glandular epithelial cells, consistent with the predominantly nuclear localization of YTHDC1 as an m6A RNA reader involved in RNA processing and gene expression. This YTHDC1 Antibody, a Nuclear m6A Reader Protein Antibody, is well suited for studies of epitranscriptomic regulation and YTHDC1 expression in colorectal cancer.

YTHDC1 Antibody Human Testicular Cancer IHC. Immunohistochemical analysis of YTHDC1 Antibody / Nuclear m6A Reader Protein Antibody in FFPE human testicular cancer tissue. Following heat-induced epitope retrieval in pH 8.0 EDTA buffer, sections were stained with YTHDC1 antibody at 2 ug/ml and detected using an HRP-conjugated secondary antibody with DAB chromogen. Predominantly nuclear staining is observed in the neoplastic cells, with weaker cytoplasmic staining in some areas, consistent with the primary nuclear localization of YTHDC1 and its role as an m6A RNA reader involved in RNA processing and gene regulation. This YTHDC1 Antibody, a Nuclear m6A Reader Protein Antibody, is well suited for investigating epitranscriptomic regulation and YTHDC1 expression in testicular cancer tissues.

YTHDC1 Antibody SiHa Cell IF. Immunofluorescence analysis of YTHDC1 Antibody / Nuclear m6A Reader Protein Antibody in SiHa cells. Cells were subjected to enzyme antigen retrieval, stained with YTHDC1 antibody at 5 ug/ml and co-labeled with an alpha tubulin antibody. YTHDC1 is shown in red, alpha tubulin in green and nuclei were counterstained with DAPI. The staining demonstrates predominant nuclear localization of YTHDC1, consistent with its role as a nuclear m6A reader that regulates RNA splicing, mRNA export and epitranscriptomic gene regulation. This YTHDC1 Antibody, a Nuclear m6A Reader Protein Antibody, is suitable for investigating subcellular localization and RNA processing pathways by immunofluorescence.

YTHDC1 Antibody Rat Brain IHC. Immunohistochemical analysis of YTHDC1 Antibody / Nuclear m6A Reader Protein Antibody in FFPE rat brain tissue. Following heat-induced epitope retrieval in pH 8.0 EDTA buffer, sections were stained with YTHDC1 antibody at 2 ug/ml and detected using an HRP-conjugated secondary antibody with DAB chromogen. Strong nuclear staining is observed throughout the brain tissue, consistent with the predominantly nuclear localization of YTHDC1 as an m6A RNA reader involved in RNA processing and gene regulation. This YTHDC1 Antibody, a Nuclear m6A Reader Protein Antibody, is suitable for investigating nuclear RNA metabolism and epitranscriptomic regulation in tissue sections.

YTHDC1 Antibody Rat Testis IHC. Immunohistochemical analysis of YTHDC1 Antibody / Nuclear m6A Reader Protein Antibody in FFPE rat testis tissue. Following heat-induced epitope retrieval in pH 8.0 EDTA buffer, sections were stained with YTHDC1 antibody at 2 ug/ml and detected using an HRP-conjugated secondary antibody with DAB chromogen. Strong predominantly nuclear staining is observed in spermatogenic cells within the seminiferous tubules, consistent with the nuclear localization of YTHDC1 and its established role in m6A-dependent RNA processing during germ cell development. This YTHDC1 Antibody, a Nuclear m6A Reader Protein Antibody, is well suited for studies of RNA methylation, spermatogenesis and epitranscriptomic regulation in reproductive tissues.

YTHDC1 Antibody Human, Rat and Mouse WB. Western blot analysis of YTHDC1 Antibody / Nuclear m6A Reader Protein Antibody detected endogenous YTHDC1 in whole cell lysates. Lane 1: human RT4 cells; Lane 2: human K562 cells; Lane 3: human HEL cells; Lane 4: rat C6 cells; Lane 5: mouse Neuro-2a cells. A rabbit polyclonal YTHDC1 antibody was used at 0.5 ug/ml. A prominent band is detected at approximately 110 kDa, although the predicted molecular weight of YTHDC1 is approximately 85 kDa. The higher apparent molecular weight is consistent with the anomalous migration reported for YTHDC1. This YTHDC1 Antibody, a Nuclear m6A Reader Protein Antibody, demonstrates cross-species detection suitable for studies of RNA methylation, RNA processing and epitranscriptomic regulation.

YTHDC1 Antibody RT4 Cell IP. Immunoprecipitation of YTHDC1 Antibody / Nuclear m6A Reader Protein Antibody from RT4 whole cell lysate followed by Western blot analysis. Lane 1: RT4 input lysate (30 ug); Lane 2: rabbit control IgG immunoprecipitation; Lane 3: YTHDC1 antibody immunoprecipitation using 2 ug antibody with 500 ug RT4 lysate. Immunoblot detection was performed using the same YTHDC1 antibody at 0.5 ug/ml. A specific band is detected at approximately 110 kDa, despite a predicted molecular weight of approximately 85 kDa, confirming efficient enrichment of endogenous YTHDC1. This YTHDC1 Antibody, a Nuclear m6A Reader Protein Antibody, is suitable for immunoprecipitation studies of m6A RNA-binding complexes and nuclear RNA processing.