Flow cytometric analysis of Human EpCAM expression on HT-29 cells. Cells from the HT-29 (Human colorectal adenocarcinoma epithelial cell, right) or Sp2/0-Ag14 (Mouse hybridoma, left) were stained with Pacific Blue Mouse IgG2b Isotype Control (black line histogram) and SDT Pacific Blue Mouse Anti-Human EpCAM Antibody (red line histogram) at 5 μl/test, cells without incubation with primary antibody and secondary antibody (blue line histogram) were used as unlabeled control. Flow cytometry and data analysis were performed using Agilent NovoCyte Quanteon and FlowJo™ software.
Product Details
Product Details
Product Specification
| Host | Mouse |
| Antigen | EpCAM |
| Location | Cell membrane |
| Accession | P16422 |
| Clone Number | S-R464 |
| Antibody Type | Mouse mAb |
| Isotype | IgG2b |
| Isotype Control | S0B1581 |
| Application | FCM |
| Reactivity | Hu |
| Positive Sample | HT-29 |
| Purification | Protein A |
| Concentration | 0.2 mg/ml |
| Conjugation | Pacific Blue |
| Physical Appearance | Liquid |
| Storage Buffer | PBS, 1% BSA, 0.09% sodium azide |
| Stability & Storage | 12 months from date of receipt / reconstitution, 2 to 8 °C as supplied |
Dilution
| application | dilution | species |
| FCM | 5μl per million cells in 100μl volume | Hu |
Background
EpCAM (epithelial cell adhesion molecule, CD326) is a 35–40 kDa type-I transmembrane glycoprotein expressed on most epithelia, where it first assembles into cis-dimers that further cluster into tetramers to support homotypic cell–cell contacts, and then—through sequential proteolytic cleavage—releases its intracellular domain (EpICD) that partners with β-catenin, FHL2 and LEF1 to enter the nucleus and drive Wnt-dependent transcription of genes controlling proliferation, stemness and epithelial-to-mesenchymal transition, thereby functioning not merely as an adhesion molecule but as a dynamic signaling hub that is highly up-regulated in most carcinomas, marks circulating tumor and cancer stem cells, and serves as both a prognostic biomarker and a therapeutic target while mutations that truncate or mis-localize the protein underlie the severe congenital diarrhea disorder tufting enteropathy.
Picture
Picture
FC
