C4.4A (Ly6/PLAUR domain-containing protein 3, LYPD3) is a tumorigenic and high-glycosylated cell surface protein that has been proven to be linked with the carcinogenic effects in different solid tumors. The elevated expression of LYPD3 is not only demonstrated to be associated with lung adenocarcinoma carcinogenesis and poor prognosis but also there is evidence that LYPD3 can lead to the initiation and development of cancers and the chemoresistance of metastatic cancers by impacting the proliferation and apoptosis of the tumor, which are involved in many important regulatory mechanisms of cancers. LYPD3 can be the ideal target for the therapy method and early detection of AML.
Background References
1. Hu T et al. LYPD3, a New Biomarker and Therapeutic Target for Acute Myelogenous Leukemia. Front Genet. 2022 Mar
2. Hu P et al. Elevated Expression of LYPD3 Is Associated with Lung Adenocarcinoma Carcinogenesis and Poor Prognosis. DNA Cell Biol. 2020 Apr
GPI-anchored metastasis-associated protein C4.4A homolog antibody
GPI-anchored metastasis-associated protein homolog antibody
Ly6/PLAUR domain-containing protein 3 antibody
Lypd3 antibody
LYPD3_HUMAN antibody
Matrigel-induced gene C4 protein antibody
MIG-C4 antibody
SHINC3 antibody
Images
Western blot analysis of LYPD3 on different lysates with Rabbit anti-LYPD3 antibody (HA721332) at 1/1,000 dilution.
Lane 1: SK-Br-3 cell lysate Lane 2: MCF-7 cell lysate Lane 3: A431 cell lysate
Lysates/proteins at 10 µg/Lane.
Predicted band size: 36 kDa Observed band size: 90 kDa
Exposure time: 1 minute 17 seconds;
4-20% SDS-PAGE gel.
Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA721332) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:200,000 dilution was used for 1 hour at room temperature.
Immunohistochemical analysis of paraffin-embedded human esophagus tissue with Rabbit anti-LYPD3 antibody (HA721332) at 1/2,000 dilution.
The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA721332) at 1/2,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
Immunohistochemical analysis of paraffin-embedded human tonsil tissue with Rabbit anti-LYPD3 antibody (HA721332) at 1/2,000 dilution.
The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA721332) at 1/2,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
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