eprintid: 11090 rev_number: 7 eprint_status: archive userid: 1993 dir: disk0/00/01/10/90 datestamp: 2021-09-09 09:12:43 lastmod: 2021-09-09 09:12:43 status_changed: 2021-09-09 09:12:43 type: article metadata_visibility: show creators_name: Muhamad Arif Budiman, MAB creators_id: arifbudiman@uhamka.ac.id creators_orcid: 0000-0002-7202-0735 title: HUMAN SERUM FOLATE CAN BE MEASURED USING FOLATE BINDING PROTEIN LINKED TO ENZYME-LABELED PROTEIN LIGAND BINDING ASSAY (ELPLBA) AS WELL AS ELISA ispublished: pub subjects: QD subjects: R1 divisions: 11201 abstract: Background: Folate is an important substance used for purine and pyrimidine nucleotide synthesis. One measurement of folate that already establishes is using ELISA (Enzymelinked immunosorbent assay) method. Folate binding protein is a protein that can bind folate,therefore it considered can be used as a tool that can replace antibody dependent ELISA method. Objectives: The aim of this research was to create a method for folate measurement in serum called Enzyme-labeled protein ligand binding assay (ELPLBA) by replacing antibody as used in ELISA method with folate binding protein (FBP) that purified from the whey of milk. Methods: The method is tested using 20 serum samples and compared to ELISA. Folate binding protein was purified from bovine's milk using ammonium sulfate up to 90% saturated, DEAE-cellulose anion exchange chromatography and affinity chromatography. SDS-PAGE and western blot were used to establish the protein band of FBP that has molecular weight of ~25-35 kDa. ELPLBA was arranged with stationary phase using aminohexyl-agarose, and folic acid linked on it using carbodiimide. Results: The result show there was no significant difference of folate concentration between ELPLBA (14.804 ± 2.795) and ELISA method (13.859 ± 3.638), p = 0.363. 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