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	<title>Cell Pellets &#8211; Apicell</title>
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	<link>https://www.apicells.com</link>
	<description>Production &#38; exploitation of mammalian cells</description>
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	<url>https://www.apicells.com/wp-content/uploads/2023/11/cropped-cropped-APICELLS-Logo-B-32x32.png</url>
	<title>Cell Pellets &#8211; Apicell</title>
	<link>https://www.apicells.com</link>
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	<item>
		<title>CV-1 Cells Pellets</title>
		<link>https://www.apicells.com/product/cv-1-cells-pellets/</link>
					<comments>https://www.apicells.com/product/cv-1-cells-pellets/#respond</comments>
		
		<dc:creator><![CDATA[Florent Rullière]]></dc:creator>
		<pubDate>Mon, 19 Feb 2018 14:34:34 +0000</pubDate>
				<guid isPermaLink="false">http://www.apicells.com/?post_type=product&#038;p=346</guid>

					<description><![CDATA[CV-1 cell line This is a pseudodiploid, male African green monkey cell line. The modal chromosome number was 60, occurring in 48% of cells, and the rate of polyploidy was at 4.4%. Only a few markers were found., Of these M1, a probable deleted N11, was found in all cells examined; M3 of unknown origin [&#8230;]]]></description>
										<content:encoded><![CDATA[<p><strong>CV-1 cell line</strong><br />
This is a pseudodiploid, male African green monkey cell line. The modal chromosome number was 60, occurring in 48% of cells, and the rate of polyploidy was at 4.4%. Only a few markers were found., Of these M1, a probable deleted N11, was found in all cells examined; M3 of unknown origin was in some cells; and the remaining 2 to 3 others of unknown origins were found only once., N11 was uniformly single copied, and N16 was also single copied in most cells. Both X and Y chromosomes were also detected in every cell.<br />
Derivation<br />
The CV-1 cell line was derived from the kidney of a male adult African green monkey by F.C. Jensen, et al. in March, 1964 for use in Rous sarcoma virus transformation studies.</p>
<p><strong>CV-1 cells&nbsp;Production</strong><br />
CV-1 cells are grown in cell-factories under GLP conditions in our facility in Mons, Belgium.</p>
<p>Cell pellets are prepared by low speed centrifugation, rinsed with phosphate buffer saline, snap frozen in liquid nitrogen and stored at -85°C.</p>
<p>The cell pellets are not prepared in aseptic conditions and are not intended to be used as seed for a new culture.</p>
<p><strong>Quality Control</strong><br />
Cultures are screened for the presence of bacteries, yeast, fungi and mycoplasma (DNA amplification).</p>
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		<item>
		<title>K562 Cell Pellets</title>
		<link>https://www.apicells.com/product/k562-cell-pellets/</link>
		
		<dc:creator><![CDATA[Florent Rullière]]></dc:creator>
		<pubDate>Thu, 13 Apr 2017 12:21:43 +0000</pubDate>
				<guid isPermaLink="false">http://new.apicells.com/?post_type=product&#038;p=157</guid>

					<description><![CDATA[Our cells pellets are produced from cells harvest in exponential phase.]]></description>
										<content:encoded><![CDATA[<p><strong>K562 cell</strong><br />
The continuous cell line K-562 was established by Lozzio and Lozzio from the pleural effusion of a 53-year-old female with chronic myelogenous leukemia in terminal blast crises.<br />
The cell population has been characterized as highly undifferentiated and of the granulocytic series.<br />
Studies conducted by Anderson, et al., on the surface membrane properties led to the conclusion that the K-562 was a human erythroleukemia line. The K-562 cell line has attained widespread use as a highly sensitive in vitro target for the natural killer assay.<br />
See Pross, et al. for a detailed analysis of the in vitro assay of NK cells including the mathematics of quantitation of NK cell activity.<br />
K-562 blasts are multipotential, hematopoietic malignant cells that spontaneously differentiate into recognizable progenitors of the erythrocytic, granulocytic and monocytic series.<br />
The effect of inducers on sublines derived from the original K-562 cell line have been reviewed by Koeffler and Golde. Cultures from the ATCC stock have been shown to exhibit this sensitivity for assessing human natural killer activity.<br />
Karyological studies on various K-562 sublines have been classified into three groups (A,B,C) by Dimery, et al.<br />
The strain obtained by the ATCC most closely resembles the B population. Occurrence of the Philadelphia chromosome, however, was of much lower frequency; none detected in 15 metaphases examined.</p>
<p><strong>K562 cells Production</strong><br />
K562 cells are grown in sonoperfused fedbatch (cytostat) mode at a constant concentration of 5&#215;10<sup>6</sup> cells/ml (cell viability: 93%-99%) under GLP conditions in our facility in Mons, Belgium. Cells are harvested in exponential phase.</p>
<p>Cell pellets are prepared by low speed centrifugation, rinsed with phosphate buffer saline, snap frozen in liquid nitrogen and stored at -85°C.</p>
<p>The cell pellets are not prepared in aseptic conditions and are not intended to be used as seed for a new culture.</p>
<p><strong>Research Use Only</strong><br />
Our K562 cell pellets are used by research or production entities worldwide for the study of biochemical processing, high throughput screening or purification of biological material from human origin. For published papers reporting the use of our extract, please check out our references list</p>
<p><strong>Quality Control</strong><br />
Cultures are screened for the presence of bacteries, yeast, fungi and mycoplasma (DNA amplification). Sera used in the culture medium are CE certified from South American origin.</p>
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		<item>
		<title>HUT-78 Cell Pellets</title>
		<link>https://www.apicells.com/product/hut-78-cell-pellets/</link>
		
		<dc:creator><![CDATA[Florent Rullière]]></dc:creator>
		<pubDate>Thu, 13 Apr 2017 12:18:18 +0000</pubDate>
				<guid isPermaLink="false">http://new.apicells.com/?post_type=product&#038;p=154</guid>

					<description><![CDATA[Our cells pellets are produced from cells harvest in exponential phase.]]></description>
										<content:encoded><![CDATA[<p><strong>HUT-78 cell</strong><br />
Derived from the peripheral blood of a patient with Sezary syndrome. The line has the properties of a mature human T cell with helper/inducer activity. It releases IL-2 and has receptors for IL-2. The growth rate is stimulated by IL-2. TNF alpha is an autocrine growth factor for HUT-78.</p>
<p><strong>HUT-78 cells&nbsp;Production</strong><br />
HUT-78 cells are grown in sonoperfused fedbatch (cytostat) mode at a constant concentration of 5&#215;10<sup>6</sup> cells/ml (cell viability: 93%-99%) under GLP conditions in our facility in Mons, Belgium. Cells are harvested in exponential phase.</p>
<p>Cell pellets are prepared by low speed centrifugation, rinsed with phosphate buffer saline, snap frozen in liquid nitrogen and stored at -85°C.</p>
<p>The cell pellets are not prepared in aseptic conditions and are not intended to be used as seed for a new culture.</p>
<p><strong>Research Use Only</strong><br />
Our HUT-78 cell pellets are used by research or production entities worldwide for the study of biochemical processing, high throughput screening or purification of biological material from human origin. For published papers reporting the use of our extract, please check out our references list</p>
<p><strong>Quality Control</strong><br />
Cultures are screened for the presence of bacteries, yeast, fungi and mycoplasma (DNA amplification). Sera used in the culture medium are CE certified from South American origin.</p>
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		<item>
		<title>U937 Cell Pellets</title>
		<link>https://www.apicells.com/product/u937-cell-pellets/</link>
		
		<dc:creator><![CDATA[Florent Rullière]]></dc:creator>
		<pubDate>Thu, 13 Apr 2017 12:18:04 +0000</pubDate>
				<guid isPermaLink="false">http://new.apicells.com/?post_type=product&#038;p=151</guid>

					<description><![CDATA[Our cells pellets are produced from cells harvest in exponential phase.]]></description>
										<content:encoded><![CDATA[<p><strong>U937 cell</strong><br />
U-937 cells are a model cell line used in biomedical research. They were isolated from the histiocytic lymphoma of a 37 year old male patient and are used to study the behaviour and differentiation of monocytes. U937 cells mature and differentiate in response to a number of soluble stimuli, adopting the morphology and characteristics of mature macrophages.</p>
<p><strong>U937 cells&nbsp;Production</strong><br />
U937 cells are grown in sonoperfused fedbatch (cytostat) mode at a constant concentration of 5&#215;10<sup>6</sup> cells/ml (cell viability: 93%-99%) under GLP conditions in our facility in Mons, Belgium. Cells are harvested in exponential phase.</p>
<p>Cell pellets are prepared by low speed centrifugation, rinsed with phosphate buffer saline, snap frozen in liquid nitrogen and stored at -85°C.</p>
<p>The cell pellets are not prepared in aseptic conditions and are not intended to be used as seed for a new culture.</p>
<p><strong>Research Use Only</strong><br />
Our U937 cell pellets are used by research or production entities worldwide for the study of biochemical processing, high throughput screening or purification of biological material from human origin. For published papers reporting the use of our extract, please check out our references list</p>
<p><strong>Quality Control</strong><br />
Cultures are screened for the presence of bacteries, yeast, fungi and mycoplasma (DNA amplification). Sera used in the culture medium are CE certified from South American origin.</p>
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		<item>
		<title>L363 Cell Pellets</title>
		<link>https://www.apicells.com/product/l363-cell-pellets/</link>
		
		<dc:creator><![CDATA[Florent Rullière]]></dc:creator>
		<pubDate>Thu, 13 Apr 2017 12:14:56 +0000</pubDate>
				<guid isPermaLink="false">http://new.apicells.com/?post_type=product&#038;p=148</guid>

					<description><![CDATA[Our cells pellets are produced from cells harvest in exponential phase.]]></description>
										<content:encoded><![CDATA[<p><strong>L363&nbsp;cell</strong><br />
Human plasma cell leukemia established from the peripheral blood of a 36-year-old woman with plasma cell leukemia (IgG) in 1977; cells were described to be EBNA-negative and to express mRNA for proto-oncogene bcl-2 confirmed as human with IEF of AST, LDH, PEP B.</p>
<p><strong>L363&nbsp;cells&nbsp;Production</strong><br />
L363&nbsp;cells are grown in sonoperfused fedbatch (cytostat) mode at a constant concentration of 5&#215;10<sup>6</sup> cells/ml (cell viability: 93%-99%) under GLP conditions in our facility in Mons, Belgium. Cells are harvested in exponential phase.</p>
<p>Cell pellets are prepared by low speed centrifugation, rinsed with phosphate buffer saline, snap frozen in liquid nitrogen and stored at -85°C.</p>
<p>The cell pellets are not prepared in aseptic conditions and are not intended to be used as seed for a new culture.</p>
<p><strong>Research Use Only</strong><br />
Our L363 cell pellets are used by research or production entities worldwide for the study of biochemical processing, high throughput screening or purification of biological material from human origin. For published papers reporting the use of our extract, please check out our references list</p>
<p><strong>Quality Control</strong><br />
Cultures are screened for the presence of bacteries, yeast, fungi and mycoplasma (DNA amplification). Sera used in the culture medium are CE certified from South American origin.</p>
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		<item>
		<title>BV173 Cell Pellets</title>
		<link>https://www.apicells.com/product/bv173-cell-pellets/</link>
		
		<dc:creator><![CDATA[Florent Rullière]]></dc:creator>
		<pubDate>Thu, 13 Apr 2017 10:12:47 +0000</pubDate>
				<guid isPermaLink="false">http://new.apicells.com/?post_type=product&#038;p=128</guid>

					<description><![CDATA[Our cells pellets are produced from cells harvest in exponential phase.]]></description>
										<content:encoded><![CDATA[<p><strong>BV173 cell</strong><br />
The BV173 cell line was established from&nbsp;a B cell precursor leukemia.</p>
<p><strong>BV173 cells&nbsp;Production</strong><br />
BV173 cells are grown in sonoperfused fedbatch (cytostat) mode at a constant concentration of 5&#215;10<sup>6</sup> cells/ml (cell viability: 93%-99%) under GLP conditions in our facility in Mons, Belgium. Cells are harvested in exponential phase.</p>
<p>Cell pellets are prepared by low speed centrifugation, rinsed with phosphate buffer saline, snap frozen in liquid nitrogen and stored at -85°C.</p>
<p>The cell pellets are not prepared in aseptic conditions and are not intended to be used as seed for a new culture.</p>
<p><strong>Research Use Only</strong><br />
Our BV173 cell pellets are used by research or production entities worldwide for the study of biochemical processing, high throughput screening or purification of biological material from human origin. For published papers reporting the use of our extract, please check out our references list</p>
<p><strong>Quality Control</strong><br />
Cultures are screened for the presence of bacteries, yeast, fungi and mycoplasma (DNA amplification). Sera used in the culture medium are CE certified from South American origin.</p>
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		<title>HL-60 Cell Pellets</title>
		<link>https://www.apicells.com/product/hl-60-cell-pellets/</link>
		
		<dc:creator><![CDATA[Florent Rullière]]></dc:creator>
		<pubDate>Thu, 13 Apr 2017 10:05:52 +0000</pubDate>
				<guid isPermaLink="false">http://new.apicells.com/?post_type=product&#038;p=125</guid>

					<description><![CDATA[Our cells pellets are produced from cells harvest in exponential phase.]]></description>
										<content:encoded><![CDATA[<p><strong>HL-60 cell</strong><br />
The HL-60 cell line was derived from a promyeloblast. The line was established from cells taken from a 36 years old female patient suffering of an acute promyelocytic leukemia.</p>
<p><strong>HL-60 cells&nbsp;Production</strong><br />
HL-60 cells are grown in sonoperfused fedbatch (cytostat) mode at a constant concentration of 5&#215;10<sup>6</sup> cells/ml (cell viability: 93%-99%) under GLP conditions in our facility in Mons, Belgium. Cells are harvested in exponential phase.</p>
<p>Cell pellets are prepared by low speed centrifugation, rinsed with phosphate buffer saline, snap frozen in liquid nitrogen and stored at -85°C.</p>
<p>The cell pellets are not prepared in aseptic conditions and are not intended to be used as seed for a new culture.</p>
<p><strong>Research Use Only</strong><br />
Our HL-60 cell pellets are used by research or production entities worldwide for the study of biochemical processing, high throughput screening or purification of biological material from human origin. For published papers reporting the use of our extract, please check out our references list</p>
<p><strong>Quality Control</strong><br />
Cultures are screened for the presence of bacteries, yeast, fungi and mycoplasma (DNA amplification). Sera used in the culture medium are CE certified from South American origin.</p>
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		<title>RAMOS Cell Pellets</title>
		<link>https://www.apicells.com/product/ramos-cell-pellets/</link>
		
		<dc:creator><![CDATA[Florent Rullière]]></dc:creator>
		<pubDate>Thu, 13 Apr 2017 10:03:17 +0000</pubDate>
				<guid isPermaLink="false">http://new.apicells.com/?post_type=product&#038;p=122</guid>

					<description><![CDATA[Our cells pellets are produced from cells harvest in exponential phase.]]></description>
										<content:encoded><![CDATA[<p><strong>RAMOS cell</strong><br />
The RAMOS cell line was derived from a B lymphocyte. The line was established from cells taken from a 3 years old male patient suffering of a Burkitt&#8217;s lymphoma.</p>
<p><strong>RAMOS cells&nbsp;Production</strong><br />
RAMOS cells are grown in sonoperfused fedbatch (cytostat) mode at a constant concentration of 5&#215;10<sup>6</sup> cells/ml (cell viability: 93%-99%) under GLP conditions in our facility in Mons, Belgium. Cells are harvested in exponential phase.</p>
<p>Cell pellets are prepared by low speed centrifugation, rinsed with phosphate buffer saline, snap frozen in liquid nitrogen and stored at -85°C.</p>
<p>The cell pellets are not prepared in aseptic conditions and are not intended to be used as seed for a new culture.</p>
<p><strong>Research Use Only</strong><br />
Our RAMOS cell pellets are used by research or production entities worldwide for the study of biochemical processing, high throughput screening or purification of biological material from human origin. For published papers reporting the use of our extract, please check out our references list</p>
<p><strong>Quality Control</strong><br />
Cultures are screened for the presence of bacteries, yeast, fungi and mycoplasma (DNA amplification). Sera used in the culture medium are CE certified from South American origin.</p>
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		<title>MOLT-4 Cell Pellets</title>
		<link>https://www.apicells.com/product/molt-4-cell-pellets/</link>
		
		<dc:creator><![CDATA[Florent Rullière]]></dc:creator>
		<pubDate>Thu, 13 Apr 2017 09:57:36 +0000</pubDate>
				<guid isPermaLink="false">http://new.apicells.com/?post_type=product&#038;p=119</guid>

					<description><![CDATA[Our cells pellets are produced from cells harvest in exponential phase.]]></description>
										<content:encoded><![CDATA[<p><strong>MOLT-4 cell</strong><br />
The MOLT-4 cell line was derived from a T lymphoblast. The line was established from cells taken from a 19 years old male patient suffering of a acute lymphoblastic leukemia in relapse.</p>
<p><strong>MOLT-4 cells&nbsp;Production</strong><br />
MOLT-4 cells are grown in sonoperfused fedbatch (cytostat) mode at a constant concentration of 5&#215;10<sup>6</sup> cells/ml (cell viability: 93%-99%) under GLP conditions in our facility in Mons, Belgium. Cells are harvested in exponential phase.</p>
<p>Cell pellets are prepared by low speed centrifugation, rinsed with phosphate buffer saline, snap frozen in liquid nitrogen and stored at -85°C.</p>
<p>The cell pellets are not prepared in aseptic conditions and are not intended to be used as seed for a new culture.</p>
<p><strong>Research Use Only</strong><br />
Our MOLT-4 cell pellets are used by research or production entities worldwide for the study of biochemical processing, high throughput screening or purification of biological material from human origin. For published papers reporting the use of our extract, please check out our references list</p>
<p><strong>Quality Control</strong><br />
Cultures are screened for the presence of bacteries, yeast, fungi and mycoplasma (DNA amplification). Sera used in the culture medium are CE certified from South American origin.</p>
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		<title>Jurkat Cell Pellets</title>
		<link>https://www.apicells.com/product/jurkat-cell-pellets/</link>
		
		<dc:creator><![CDATA[Florent Rullière]]></dc:creator>
		<pubDate>Thu, 13 Apr 2017 09:48:06 +0000</pubDate>
				<guid isPermaLink="false">http://new.apicells.com/?post_type=product&#038;p=115</guid>

					<description><![CDATA[Our cells pellets are produced from cells harvest in exponential phase.]]></description>
										<content:encoded><![CDATA[<p><strong>Jurkat cell</strong><br />
The Jurkat cell line was established from the peripheral blood of a 14 year old boy by Schneider et al., and was originally designated JM.</p>
<p><strong>Jurkat cells Production</strong><br />
Jurkat cells are grown in sonoperfused fedbatch (cytostat) mode at a constant concentration of 5&#215;10<sup>6</sup> cells/ml (cell viability: 93%-99%) under GLP conditions in our facility in Mons, Belgium. Cells are harvested in exponential phase.</p>
<p>Cell pellets are prepared by low speed centrifugation, rinsed with phosphate buffer saline, snap frozen in liquid nitrogen and stored at -85°C.</p>
<p>The cell pellets are not prepared in aseptic conditions and are not intended to be used as seed for a new culture.</p>
<p><strong>Research Use Only</strong><br />
Our Jurkat cell pellets are used by research or production entities worldwide for the study of biochemical processing, high throughput screening or purification of biological material from human origin. For published papers reporting the use of our extract, please check out our references list</p>
<p><strong>Quality Control</strong><br />
Cultures are screened for the presence of bacteries, yeast, fungi and mycoplasma (DNA amplification). Sera used in the culture medium are CE certified from South American origin.</p>
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