Recombinant Human EpCAM/TROP1 Fc Chimera Avi-tag Protein, CF Summary
Additional Information |
Biotinylated |
Details of Functionality |
Measured by its binding ability in a functional ELISA. When Human EpCAM/TROP1 Affinity Purified Polyclonal Antibody
(Catalog #
AF960)
is immobilized at 0.25 µg/mL (100 µL/well), it binds to Biotinylated Recombinant Human EpCAM/TROP‑1 Fc Chimera Avi-tag with an ED 50 of 1-6 ng/mL. Measured by the ability of the immobilized protein to support the adhesion of the L Cells mouse fibroblast cell line. The ED 50 for this effect is 0.7-2.8 μg/mL. |
Source |
Human embryonic kidney cell, HEK293-derived human EpCAM/TROP1 protein Human EpCAM/TROP-1 (Gln24-Lys265) Accession # P16422.2 | IEGRMD | Human IgG1 (Pro100-Lys330) | Avi-tag | |
|
Accession # |
|
N-terminal Sequence |
Gln24, inferred from deblocking reaction revealing Glu25. |
Structure / Form |
Disulfide-linked homodimer, biotinylated via Avi-tag |
Protein/Peptide Type |
Recombinant Proteins |
Purity |
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining. |
Endotoxin Note |
<0.10 EU per 1 μg of the protein by the LAL method. |
Applications/Dilutions
Dilutions |
|
Theoretical MW |
56 kDa. Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors. |
SDS-PAGE |
55-75 kDa, under reducing conditions |
Packaging, Storage & Formulations
Storage |
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 3 months, -20 to -70 °C under sterile conditions after reconstitution.
|
Buffer |
Lyophilized from a 0.2 μm filtered solution in PBS with Trehalose. |
Purity |
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining. |
Reconstitution Instructions |
Reconstitute at 500 μg/mL in PBS. |
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Recombinant Human EpCAM/TROP1 Fc Chimera Avi-tag Protein, CF
Background
Epithelial
Cellular Adhesion Molecule (EpCAM), also known as KS1/4, gp40, GA733-2, 17-1A,
and TROP‑1,
is a transmembrane glycoprotein originally identified as a tumor-associated
antigen due to its high expression level in rapidly growing epithelial tumors (1).
EpCAM is one of several cell adhesion molecules (CAMs) that does not share the
structural patterns found in the four major CAM families. Human EpCAM is
composed of an extracellular domain (ECD) with two epidermal-growth-factor-like
(EGF‑like)
repeats, a single transmembrane domain, and a highly charged, short cytoplasmic
domain. Within the mature ECD, human EpCAM shares 81% and 82% amino acid
sequence identity with mouse and rat EpCAM respectively. During embryonic
development, EpCAM is detected in fetal lung, kidney, liver, pancreas, skin,
and germ cells (2). In adults, human EpCAM is detected in basolateral cell
membranes of all simple, pseudo-stratified, and transitional epithelia, but is
not detected in normal squamous stratified epithelia, mesenchymal tissue,
muscular tissue, neuro-endocrine tissue, or lymphoid tissue (2). EpCAM
expression has been found to increase in actively proliferating epithelia
tissues and in human malignant neoplasias arising from squamousal epithelia (2,
3). It has been found that EpCAM is present on normal hepatic stem cells and is
increased on cells with advanced cirrhosis due to the cells' proliferation
through autocrine activation of Wnt signaling (4). Additionally, EpCAM may be
beneficial in the early diagnosis of hepatocellular carcinoma (HCC) since HCC
typically originates from a cirrhotic background (4). EpCAM has been shown
function as a homophilic Ca2+ independent adhesion molecule (3). Homophilic
adhesion via EpCAM requires the interaction of both EGFlike repeats, with the
first EGFlike repeat mediating reciprocal interaction between EpCAM molecules
on opposing cells, while the second repeat is involved in lateral interaction
of EpCAM. Lateral interaction of EpCAM lead to the formation of dimers and
tetramers (5). During homophilic adhesion the cytoplasmic tail of EpCAM
interacts with the actin cytoskeleton via a direct association alpha actinin (6).
- Kloudova, K. et al. (2016) Oncotarget. 7:46120.
- Huang, L. et al. (2018) Int. J. Mol. Med. 42:1771.
- Munz, M. et al. (2009). J. Cancer Res. 69:5627.
- Khosla, R. et al. (2017). Stem Cells Trans. Med. 6:807.
- Balzar, M. et al. (2001) Mol. Cell. Biol. 21:2570.
- Balzar, M. et al. (1998) Mol. Cell. Biol. 18:4388.
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