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Read our guarantee »Products:Tags & Cell Markers >> Cell Type Markers >> Tumor Associated
Anti-EpCAM antibody [B29.1 (VU-ID9)] (FITC)
See all EpCAM products (24) ...
Mouse monoclonal [B29.1 (VU-ID9)] to EpCAM (FITC)
FITC
Fluorescein (FITC) conjugated at a ratio of 6 moles of Fluorescein to 1 mole of antibody. Maximum excitation of FITC occurs at wavelength 492 nm and maximum emission occurs at wavelength 520 nm.
This antibody reacts with a 40 kD cell surface glycoprotein called ESA.
ICC, IHC-P, WB, IP, ICC/IFmore details
Reacts with
Human
Small cell lung carcinoma cell line.
Breast, colon carcinoma and tonsil
Liquid
Store at +4°C. Do not freeze.
pH: 7.40
Preservative: 0.1% Sodium azide
Constituent: 0.01% PBS
Concentration information loading...
Protein G purified
Monoclonal
B29.1 (VU-ID9)
IgG1
kappa
Tags & Cell Markers >> Cell Type Markers >> Epi / Endo-thelial
Tags & Cell Markers >> Cell Type Markers >> Tumor Associated
Flow Cytometry - EpCAM antibody [B29.1 (VU-ID9)] (FITC) (ab8666)
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Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - EpCAM antibody [B29.1 (VU-ID9)] (FITC) (ab8666)
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Immunocytochemistry/ Immunofluorescence-EpCAM antibody [B29.1 (VU-ID9)] (FITC)(ab8666)
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Our Abpromise guarantee covers the use of ab8666 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
ICC: Use a concentration of 5 - 10 µg/ml.(PubMed: 17417652)
IHC-P: Use a concentration of 5 - 10 µg/ml.(PubMed: 20421921)
WB: Use a concentration of 1 - 5 µg/ml.(
This product was not quality controlled in Flow Cytometry applications. However, it may be applicable for Flow Cytometry at a concentration of 1-2 µg in 0.1 ml containing 10^6 cells.)
IP: Use at an assay dependent concentration.
ICC/IF: Use a concentration of 5 - 10 µg/ml.(See Abreview.)
May act as a physical homophilic interaction molecule between intestinal epithelial cells (IECs) and intraepithelial lymphocytes (IELs) at the mucosal epithelium for providing immunological barrier as a first line of defense against mucosal infection. Plays a role in embryonic stem cells proliferation and differentiation. Up-regulates the expression of FABP5, MYC and cyclins A and E.
Highly and selectively expressed by undifferentiated rather than differentiated embryonic stem cells (ESC). Levels rapidly diminish as soon as ESC's differentiate (at protein levels). Expressed in almost all epithelial cell membranes but not on mesodermal or neural cell membranes. Found on the surface of adenocarcinoma.
Defects in EPCAM are the cause of diarrhea type 5 (DIAR5) [MIM:613217]. It is an intractable diarrhea of infancy characterized by villous atrophy and absence of inflammation, with intestinal epithelial cell dysplasia manifesting as focal epithelial tufts in the duodenum and jejunum.
Defects in EPCAM are a cause of hereditary non-polyposis colorectal cancer type 8 (HNPCC8) [MIM:613244]. HNPCC is a disease associated with marked increase in cancer susceptibility. It is characterized by a familial predisposition to early-onset colorectal carcinoma (CRC) and extra-colonic tumors of the gastrointestinal, urological and female reproductive tracts. HNPCC is reported to be the most common form of inherited colorectal cancer in the Western world. Clinically, HNPCC is often divided into two subgroups. Type I is characterized by hereditary predisposition to colorectal cancer, a young age of onset, and carcinoma observed in the proximal colon. Type II is characterized by increased risk for cancers in certain tissues such as the uterus, ovary, breast, stomach, small intestine, skin, and larynx in addition to the colon. Diagnosis of classical HNPCC is based on the Amsterdam criteria: 3 or more relatives affected by colorectal cancer, one a first degree relative of the other two; 2 or more generation affected; 1 or more colorectal cancers presenting before 50 years of age; exclusion of hereditary polyposis syndromes. The term 'suspected HNPCC' or 'incomplete HNPCC' can be used to describe families who do not or only partially fulfill the Amsterdam criteria, but in whom a genetic basis for colon cancer is strongly suspected. Note=HNPCC8 results from heterozygous deletion of 3-prime exons of EPCAM and intergenic regions directly upstream of MSH2, resulting in transcriptional read-through and epigenetic silencing of MSH2 in tissues expressing EPCAM.
Belongs to the EPCAM family.
Contains 1 thyroglobulin type-1 domain.
Hyperglycosylated in carcinoma tissue as compared with autologous normal epithelia. Glycosylation at Asn-198 is crucial for protein stability.
Lateral cell membrane. Cell junction > tight junction. Co-localizes with CLDN7 at the lateral cell membrane and tight junction.
Target information above from: UniProt accessionP16422
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Flow Cytometry - EpCAM antibody [B29.1 (VU-ID9)] (FITC) (ab8666)
![Flow Cytometry - EpCAM antibody [B29.1 (VU-ID9)] (FITC) (ab8666)](/ps/datasheet/Images/8/ab8666/ab8666_11.jpg)
Histogram plot of prostate tumour cells DU145 (green) over isotype control (red) stained with EpCam following resection.
This picture was kindly supplied as part of the review submitted by Phil Kearney.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - EpCAM antibody [B29.1 (VU-ID9)] (FITC) (ab8666)
![Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - EpCAM antibody [B29.1 (VU-ID9)] (FITC) (ab8666)](/ps/datasheet/images/8/ab8666/EpCAM-Primary-antibodies-ab8666-1.jpg)
ab8666 staining EpCAM in murine xenograft tumour derived from human DCIS cells by Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections). The sections were deparaffinized in xylene, and rehydrated in graded alcohols. Sections were then incubated at room temperature with ab8666 at 5 µg/ml. Slides were rinsed in borate buffer pH 8 and counterstained. EpCAM-FITC pseudo-colored green, 488 nm and DAPI psuedo-colored blue, 408 nm.
Image from Espina V et al, PLoS One. 2010 Apr 20;5(4):e10240, Fig 1.
Immunocytochemistry/ Immunofluorescence-EpCAM antibody [B29.1 (VU-ID9)] (FITC)(ab8666)
![Immunocytochemistry/ Immunofluorescence-EpCAM antibody [B29.1 (VU-ID9)] (FITC)(ab8666)](/ps/datasheet/images/8/ab8666/EpCAM-Primary-antibodies-ab8666-2.jpg)
ICC/IF image of ab8666 stained HepG2 cells. The cells were 4% formaldehyde fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab8666, 5µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-mouse IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
This product has been referenced in:
See all 6 publications for this product
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![Flow Cytometry - EpCAM antibody [B29.1 (VU-ID9)] (FITC) (ab8666)](/ps/datasheet/Images/8/ab8666/ab8666_11.jpg)
Histogram plot of prostate tumour cells DU145 (green) over isotype control (red) stained with EpCam following resection.
This picture was kindly supplied as part of the review submitted by Phil Kearney.
![Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - EpCAM antibody [B29.1 (VU-ID9)] (FITC) (ab8666)](/ps/datasheet/images/8/ab8666/EpCAM-Primary-antibodies-ab8666-1.jpg)
ab8666 staining EpCAM in murine xenograft tumour derived from human DCIS cells by Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections). The sections were deparaffinized in xylene, and rehydrated in graded alcohols. Sections were then incubated at room temperature with ab8666 at 5 µg/ml. Slides were rinsed in borate buffer pH 8 and counterstained. EpCAM-FITC pseudo-colored green, 488 nm and DAPI psuedo-colored blue, 408 nm.
Image from Espina V et al, PLoS One. 2010 Apr 20;5(4):e10240, Fig 1.
![Immunocytochemistry/ Immunofluorescence-EpCAM antibody [B29.1 (VU-ID9)] (FITC)(ab8666)](/ps/datasheet/images/8/ab8666/EpCAM-Primary-antibodies-ab8666-2.jpg)
ICC/IF image of ab8666 stained HepG2 cells. The cells were 4% formaldehyde fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab8666, 5µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-mouse IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
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