抗Ep CAM/CD326(上皮标记物)的Abeomics/重组小鼠单克隆抗体(克隆:rMOC-31)/20µg/12-1006

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¥3980.00
货号:12-1006
浏览量:127
品牌:Abeomics
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商品描述

Format :Purified
Amount :100 µg
Isotype :Mouse IgG1, kappa
Purification :Purified Ab with BSA and Azide at 200ug/ml
Content :200ug/ml of recombinant MAb purified by Protein A/G. Prepared in 10mM PBS with 0.05% BSA & 0.05% azide. Also available WITHOUT BSA & azide at 1.0mg/ml.
Storage condition :Store the antibody at 4°C; stable for 6 months. For long-term storage; store at -20°C. Avoid repeated freeze and thaw cycles.
Gene :EPCAM
Gene ID :4072
Uniprot ID :P16422
Alternative Name :Adenocarcinoma-associated Antigen,Cell Surface Glycoprotein Trop-1,EGP2,EGP314,EGP40,Epithelial Cell Adhesion Molecule,Epithelial Glycoprotein 314,ESA,KSA,TACD1,TROP1,Tumor-associated Calcium Signal Transducer 1 (TACSTD1),ECS-1,Epidermal Surface Antigen 1,ESA1,FLOT2,Flotillin-2,Membrane Component,Chromosome 17,Surface Marker-1 (M17S1),REG-1,Reggie-1,Reggie-2
Immunogen Information :Neuraminidase treated GLS-1 human small cell lung carcinoma cells

Binding epitope of this antibody is located in the first EGF-like repeat domain (EGF1) between amino acids 27-59 of Ep-CAM. EGP40 is a 40-43kDa transmembrane epithelial glycoprotein, also identified as epithelial specific antigen (ESA), or epithelial cellular adhesion molecule (Ep-CAM). It is expressed on baso-lateral cell surface in most simple epithelia and a vast majority of carcinomas with the exception of adult squamous epithelium, hepatocytes and gastric epithelial cells. This antibody has been used to distinguish adenocarcinoma from pleural mesothelioma and hepatocellular carcinoma. This antibody is also useful in distinguishing serous carcinomas of the ovary from mesothelioma.

Does not react with rat.

MW : 40-43kDa; Positive Control : HT29 cells or breast tumor;Flow Cytometry (0.5-1ug/million cells); Immunofluorescence (1-2ug/ml); Western Blotting (0.5-1.0ug/ml); Immunohistology (Formalin-fixed) (0.5-1.0ug/ml for 30 min at RT),(Staining of formalin-fixed tissues requires boiling tissue sections in 10mM Citrate Buffer, pH 6.0, for 10-20 min followed by cooling at RT for 20 minutes),Optimal dilution for a specific application should be determined.

For Research Use Only. Not for use in diagnostic/therapeutics procedures.

Subcellular location:Lateral cell membrane, Cell junction
Post transnational modification:Hyperglycosylated in carcinoma tissue as compared with autologous normal epithelia. Glycosylation at Asn-198 is crucial for protein stability.
BioGrid:110250.5 interactions.
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