CD66c Mouse Monoclonal Antibody(C2629)
WB | 1:500 - 1:1000 |
IHC | 1:100 - 1:500 |
IF/ICC | 1:50 - 1:100 |
FC | 1:100 - 1:200 |
Description | Mouse monoclonal to CD66c |
Specificity | Recognizes endogenous levels of CD66c protein |
Antibody Type | Primary antibody |
Imnunogen | Recombinant fusion protein of human CD66c expressed in HEK293 |
Purification | This antibody is purified through a protein G column. |
Molecular Weight | Predicted: 37 kD; Observed: 50 kD kD |
Form/Buffer | Mouse IgG1. Liquid in PBS, pH 7.3, 30% glycerol, and 0.01% sodium azide. |
Alternative Names | NCA; CarcinoembryonIC, antigen-related cell adhesion molecule 6; Non-specifIC, crossreacting antigen; Normal cross-reacting antigen; CD66c |
Gene Symbol | CEACAM6 |
Entrez Gene | 4680(Human) |
SwissProt | P40199(Human) |
*Clone Number, Reactivity, Source/Host and Clonality can be found in the product name and Key Features section above.

Western blot analysis of CD66c expression in Jurkat (A), PC12 (B), HEK293 (C), MG63 (D), C2C12 (E) whole cell lysates. (Predicted band size: 37 kD; Observed band size: 50 kD kD)

Immunohistochemical analysis of CD66c staining in human colon formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.

Immunofluorescent analysis of CD66c staining in Hela cells. Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with the primary antibody in 3% BSA-PBS and incubated overnight at 4 °C in a hidified chamber. Cells were washed with PBST and incubated with an AREX® Fluor 488 -conjugated secondary antibody (green) in PBS at room temperature in the dark. Phalloidin - AREX® Fluor 594 was used to stain Actin filaments (red). DAPI was used to stain the cell nuclei (blue).

Flow cytometric analysis of Jurkat cells using Anti-CD66c Antibody (green) and negative control (red).
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