<?xml version="1.0" encoding="UTF-8"?>
<article article-type="research-article" dtd-version="1.3" xmlns:xlink="http://www.w3.org/1999/xlink">
	<front>
		<journal-meta>
			<journal-title-group>
				<journal-title>Tạp chí Khoa học và Công nghệ</journal-title>
				<abbrev-journal-title>Khoa học &amp; Công nghệ</abbrev-journal-title>
			</journal-title-group>
			<issn pub-type="ppub">2615-9015</issn>
			<issn pub-type="epub">2615-9015</issn>
			<publisher><publisher-name>Trường Đại học Nguyễn Tất Thành</publisher-name></publisher>
		</journal-meta>
		<article-meta>
			<article-id pub-id-type="publisher-id">93610bb3-7a81-897d-8396-01a0fb55a4fd</article-id>
			<article-id pub-id-type="doi">10.55401/xz9xrv04</article-id>
			<title-group><article-title>An effective protocol for isolation and culture of mesenchymal stem cells from mouse bone marrow</article-title></title-group>
			<contrib-group>
				<contrib contrib-type="author"><string-name>Nguyen Thi Phuong</string-name></contrib><contrib contrib-type="author"><string-name>Nguyen Huu Hung</string-name></contrib>
			</contrib-group>
			<pub-date pub-type="epub"><day>23</day><month>1</month><year>2024</year></pub-date>
			<volume>1</volume>
			<issue>2</issue>
			<fpage>17</fpage>
			<lpage>20</lpage>
			<self-uri content-type="html" xlink:href="https://jst.ntt.edu.vn/articles/93610bb3-7a81-897d-8396-01a0fb55a4fd" />
			<self-uri content-type="pdf" xlink:href="https://uploadservice.ntt.edu.vn/dbOBrwZN1R_1/file/4_an_effective_protocol_for_isolation_261002-FOFG3SAac5aG.pdf" />
			<abstract><p>Bone marrow is known as the main source of isolated mesenchymal stem cells. This study has demonstrated a protocol for isolation and culture of mesenchymal stem cells from mouse bone marrow (mBM) with minimal requirement. The cells were harvested from the tibias and femurs, and then cultured in Dulbecco’s modified Eagle’s medium supplemented with fetal bovine serum. The mBM-MSCs were isolated by media changing every 8 hours in 24 hours of culture and sub-culture. Target cells subsequently were regconized by adipogenic differentiaton posibility. The study also focused on descript a simple procedure to culture BM-MSCs and the results obtained following the procedure</p></abstract>
			<kwd-group><kwd>Bone marrow</kwd><kwd>cell culture</kwd><kwd>isolation</kwd><kwd>differentiation</kwd><kwd>mesenchymal stem cells</kwd></kwd-group>
		</article-meta>
	</front>
</article>