Erfa Biotech

Carcinoembryonic antigen
Monoclonal antibody to CEA
Monoclonal syngeneic anti-idiotypic antibody to anti-carcinoembryonic antigen monoclonal antibody
 

CARCINOEMBRYONIC ANTIGEN 100 % PUR (FOR RESEARCH)

ERFA Biotech of Montreal, Canada, announces the availability of purified carcinoembryonic antigen (CEA) of the highest quality and batch consistency.

Introduction

Human neoplasms may produce and release into the circulation a variety of substances collectively referred to as tumour markers.

One such group of tumour markers, identified as oncofoetal antigens, present in embryonic and foetal tissues but not in significant amounts in healthy adults, will occasionally reappear in increased quantities during malignancy.
The most extensively studied oncodevelopmental protein, carcinoembryonic antigen, was discovered by Gold and Freedman in both foetal gut and adenocarcinoma of the colon.

CEA is a fairly typical, high-molecular weight, cell surface glycoprotein. It consists of a single polypeptide chain and carbohydrates that constitute 50-60% of CEA molecule giving rise to an unusually high degree of molecular size heterogeneity.

Antibodies induced against CEA would react with a variety of proteins present in normal tissues such as: non-specific cross-reacting antigen (NCA), NCA-II, biliary glycoprotein 1 (BGP-1), normal colon washing(NCW), and meconium antigen.

GENERAL APPLICATIONS OF CEA

Initially it was hoped that the circulating CEA level would be both a sensitive and specific marker for the presence of cancer. These hopes have largely been dispelled as clinical evidence accumulated. Thus, CEA assay cannot be used for population screening or cancer diagnosis, as it become apparent that CEA not only circulates in small quantities in normal individuals, but is not always elevated in early stages of cancer. Despite these problems, Medical literature has reported the importance of CEA assay in the management of cancer patients, both preoperatively and postoperatively, in whom the diagnosis of cancer has already been established. For example, serial CEA determinations allow initiation of antitumour chemotherapy, radiotherapy, or "second look" surgery at an earlier stage of progression of disease, when the tumor loads are small and potentially curable.

The immunoperoxidase staining of tumor tissue for CEA has also been reported in literature as a useful adjunct for pathologists. Mainly because the degree of tissue CEA staining correlates well with plasma CEA levels, the degree of tumour differentiation, the stage of disease, the histologic tumour type, and the clinical prognosis of various carcinomas. Of importance is the fact that CEA immunohistochemistry can be performed retrospectively on paraffin blocks allowing a direct comparison between the primary lesion and initially occult metastatic disease.

It has been reported that CEA is not immunogenic in patients bearing CEA-producing tumours, however, tolerance to CEA could be broken by proper immunological manipulation. Liposomal carriers are able to potentiate immunological responsiveness against weakly immunogenic antigens. It is also possible to incorporate and retain CEA within the aqueous phase of liposomal carriers and that anti-CEA antibodies could be elicited in mice immunized with liposomal CEA.


ANTIGÈNE CARCINOEMBRYONNAIRE 100 % PUR

Figure 1 : Electrophoretic mobility of CEA-Rougier (ERFA) on sodium-dodecyl-sulfate polyacrylamide gel


Ligne 1 : BSA
Ligne 2 : Bio-Rad molecular weight protein standards (92,5 kd; 66,2 kd; 31 kd; 21,5 kd)
Ligne 3 : CEA-Rougier (ERFA)
Ligne 4 : Bio-Rad molecular weight protein standards (200 kd; 116,25 kd; 92,5 kd; 66,2 kd; 45 kd)
Ligne 5 : BSA


ISOLATION AND PURIFICATION OF CEA

ERFA's CEA has been purified under the most stringent conditions. The starting material for Erfa's CEA is the richest source of CEA known: hepatic metastases from colorectal cancers. Purification proceeds through water homogenization, perchloric acid extraction, ion-exchange, affinity and gel filtration chromatographies.

PHYSICOCHEMICAL PROPERTIES

Molecular weight 180,000 by SDS-PAGE electrophoresis
60% by weight of carbohydrate
Purity100% pure and does not contain NCA; determined by SDS-PAGE and HPLC gel filtration chromatography.


POTENTIAL APPLICATIONS

(1) Structural and functional analyses of CEA molecule
(2) Preparation of anti-CEA monoclonal antibodies
(3) Preparation of anti-CEA heteroantisera
(4) Standard curves for quantitative CEA assay
(5) Cancer immunotherapy research

Delivery quantities : - 0.1 mg/vial SKU #: 76010
- 0.5 mg/vial SKU #: 76015
- 1 mg/vial SKU #: 76020