mouse anti major histocompatibility complex ii Search Results


allophycocyanin-conjugated rat anti-mouse major histocompatibility complex (mhc ii) (iabdq, i-edk  (Becton Dickinson)
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Becton Dickinson allophycocyanin-conjugated rat anti-mouse major histocompatibility complex (mhc ii) (iabdq, i-edk
Allophycocyanin Conjugated Rat Anti Mouse Major Histocompatibility Complex (Mhc Ii) (Iabdq, I Edk, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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mouse anti-mouse major histocompatibility complex (mhc) class  (Becton Dickinson)
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Becton Dickinson mouse anti-mouse major histocompatibility complex (mhc) class
Mouse Anti Mouse Major Histocompatibility Complex (Mhc) Class, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ox6 (mouse anti-rat major histocompatibility complex [mhc] class ii  (Becton Dickinson)
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rat anti-mouse major histocompatibility complex (mhc) class ii antigen antibody  (Becton Dickinson)
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Becton Dickinson rat anti-mouse major histocompatibility complex (mhc) class ii antigen antibody
Rat Anti Mouse Major Histocompatibility Complex (Mhc) Class Ii Antigen Antibody, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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fitc-conjugated mouse anti-rat major histocompatibility complex class ii  (Becton Dickinson)
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Fitc Conjugated Mouse Anti Rat Major Histocompatibility Complex Class Ii, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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pe-anti-mouse class ii major histocompatibility complex (mhc  (Becton Dickinson)
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Becton Dickinson pe-anti-mouse class ii major histocompatibility complex (mhc
T-MSCs inhibit differentiation and maturation of DCs under coculture conditions. Bone-marrow- (BM-) derived monocytes (BMCs) isolated from 8-week-old BALB/c mice were incubated with of granulocyte-macrophage colony-stimulating factor (GM-CSF) (20 ng/mL) for 12 days to induce differentiation into dendritic cells (DCs). (a) Lipopolysaccharide (LPS) (1 μ g/mL) was added for the last 2 days to induce DC maturation. (b) GM-CSF treatment induced expansion of CD11b + cells ( ** P < 0.01). (c) Tonsil-derived MSCs (T-MSCs) added at day 0, but not at day 10, inhibited upregulated expression of CD80 ( * P < 0.05) and CD86 ( ** P < 0.01) on mature DCs by direct contact. Upregulated major histocompatibility complex <t>(MHC)</t> class II expression on immature ( ** P < 0.01) and mature DCs ( ** P < 0.01) was reduced by T-MSCs, <t>but</t> <t>CD14</t> expression was not affected.
Pe Anti Mouse Class Ii Major Histocompatibility Complex (Mhc, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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mouse anti-class ii major histocompatibility complex protein (anti-mhc-ii) abs  (IQ Products)
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T-MSCs inhibit differentiation and maturation of DCs under coculture conditions. Bone-marrow- (BM-) derived monocytes (BMCs) isolated from 8-week-old BALB/c mice were incubated with of granulocyte-macrophage colony-stimulating factor (GM-CSF) (20 ng/mL) for 12 days to induce differentiation into dendritic cells (DCs). (a) Lipopolysaccharide (LPS) (1 μ g/mL) was added for the last 2 days to induce DC maturation. (b) GM-CSF treatment induced expansion of CD11b + cells ( ** P < 0.01). (c) Tonsil-derived MSCs (T-MSCs) added at day 0, but not at day 10, inhibited upregulated expression of CD80 ( * P < 0.05) and CD86 ( ** P < 0.01) on mature DCs by direct contact. Upregulated major histocompatibility complex <t>(MHC)</t> class II expression on immature ( ** P < 0.01) and mature DCs ( ** P < 0.01) was reduced by T-MSCs, <t>but</t> <t>CD14</t> expression was not affected.
Mouse Anti Class Ii Major Histocompatibility Complex Protein (Anti Mhc Ii) Abs, supplied by IQ Products, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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fitc-conjugated mouse anti-human major histocompatibility (mhc) class (hla-abc  (Becton Dickinson)
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Becton Dickinson fitc-conjugated mouse anti-human major histocompatibility (mhc) class (hla-abc
T-MSCs inhibit differentiation and maturation of DCs under coculture conditions. Bone-marrow- (BM-) derived monocytes (BMCs) isolated from 8-week-old BALB/c mice were incubated with of granulocyte-macrophage colony-stimulating factor (GM-CSF) (20 ng/mL) for 12 days to induce differentiation into dendritic cells (DCs). (a) Lipopolysaccharide (LPS) (1 μ g/mL) was added for the last 2 days to induce DC maturation. (b) GM-CSF treatment induced expansion of CD11b + cells ( ** P < 0.01). (c) Tonsil-derived MSCs (T-MSCs) added at day 0, but not at day 10, inhibited upregulated expression of CD80 ( * P < 0.05) and CD86 ( ** P < 0.01) on mature DCs by direct contact. Upregulated major histocompatibility complex <t>(MHC)</t> class II expression on immature ( ** P < 0.01) and mature DCs ( ** P < 0.01) was reduced by T-MSCs, <t>but</t> <t>CD14</t> expression was not affected.
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anti-mouse major histocompatibility complex (mhc) class i cl9013f  (Cedarlane)
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Cedarlane anti-mouse major histocompatibility complex (mhc) class i cl9013f
T-MSCs inhibit differentiation and maturation of DCs under coculture conditions. Bone-marrow- (BM-) derived monocytes (BMCs) isolated from 8-week-old BALB/c mice were incubated with of granulocyte-macrophage colony-stimulating factor (GM-CSF) (20 ng/mL) for 12 days to induce differentiation into dendritic cells (DCs). (a) Lipopolysaccharide (LPS) (1 μ g/mL) was added for the last 2 days to induce DC maturation. (b) GM-CSF treatment induced expansion of CD11b + cells ( ** P < 0.01). (c) Tonsil-derived MSCs (T-MSCs) added at day 0, but not at day 10, inhibited upregulated expression of CD80 ( * P < 0.05) and CD86 ( ** P < 0.01) on mature DCs by direct contact. Upregulated major histocompatibility complex <t>(MHC)</t> class II expression on immature ( ** P < 0.01) and mature DCs ( ** P < 0.01) was reduced by T-MSCs, <t>but</t> <t>CD14</t> expression was not affected.
Anti Mouse Major Histocompatibility Complex (Mhc) Class I Cl9013f, supplied by Cedarlane, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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fitc-anti-mouse histocompatibility complex class antigen h-2k[d  (Becton Dickinson)
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Becton Dickinson fitc-anti-mouse histocompatibility complex class antigen h-2k[d
T-MSCs inhibit differentiation and maturation of DCs under coculture conditions. Bone-marrow- (BM-) derived monocytes (BMCs) isolated from 8-week-old BALB/c mice were incubated with of granulocyte-macrophage colony-stimulating factor (GM-CSF) (20 ng/mL) for 12 days to induce differentiation into dendritic cells (DCs). (a) Lipopolysaccharide (LPS) (1 μ g/mL) was added for the last 2 days to induce DC maturation. (b) GM-CSF treatment induced expansion of CD11b + cells ( ** P < 0.01). (c) Tonsil-derived MSCs (T-MSCs) added at day 0, but not at day 10, inhibited upregulated expression of CD80 ( * P < 0.05) and CD86 ( ** P < 0.01) on mature DCs by direct contact. Upregulated major histocompatibility complex <t>(MHC)</t> class II expression on immature ( ** P < 0.01) and mature DCs ( ** P < 0.01) was reduced by T-MSCs, <t>but</t> <t>CD14</t> expression was not affected.
Fitc Anti Mouse Histocompatibility Complex Class Antigen H 2k[D, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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fitc-conjugated monoclonal rat anti-mouse major histocompatibility complex ii antibody  (Becton Dickinson)
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Becton Dickinson fitc-conjugated monoclonal rat anti-mouse major histocompatibility complex ii antibody
T-MSCs inhibit differentiation and maturation of DCs under coculture conditions. Bone-marrow- (BM-) derived monocytes (BMCs) isolated from 8-week-old BALB/c mice were incubated with of granulocyte-macrophage colony-stimulating factor (GM-CSF) (20 ng/mL) for 12 days to induce differentiation into dendritic cells (DCs). (a) Lipopolysaccharide (LPS) (1 μ g/mL) was added for the last 2 days to induce DC maturation. (b) GM-CSF treatment induced expansion of CD11b + cells ( ** P < 0.01). (c) Tonsil-derived MSCs (T-MSCs) added at day 0, but not at day 10, inhibited upregulated expression of CD80 ( * P < 0.05) and CD86 ( ** P < 0.01) on mature DCs by direct contact. Upregulated major histocompatibility complex <t>(MHC)</t> class II expression on immature ( ** P < 0.01) and mature DCs ( ** P < 0.01) was reduced by T-MSCs, <t>but</t> <t>CD14</t> expression was not affected.
Fitc Conjugated Monoclonal Rat Anti Mouse Major Histocompatibility Complex Ii Antibody, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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er-tr2 (rat anti-mouse major histocompatibility complex [mhc] class ii  (Biozol Diagnostica Vertrieb GmbH)
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Biozol Diagnostica Vertrieb GmbH er-tr2 (rat anti-mouse major histocompatibility complex [mhc] class ii
T-MSCs inhibit differentiation and maturation of DCs under coculture conditions. Bone-marrow- (BM-) derived monocytes (BMCs) isolated from 8-week-old BALB/c mice were incubated with of granulocyte-macrophage colony-stimulating factor (GM-CSF) (20 ng/mL) for 12 days to induce differentiation into dendritic cells (DCs). (a) Lipopolysaccharide (LPS) (1 μ g/mL) was added for the last 2 days to induce DC maturation. (b) GM-CSF treatment induced expansion of CD11b + cells ( ** P < 0.01). (c) Tonsil-derived MSCs (T-MSCs) added at day 0, but not at day 10, inhibited upregulated expression of CD80 ( * P < 0.05) and CD86 ( ** P < 0.01) on mature DCs by direct contact. Upregulated major histocompatibility complex <t>(MHC)</t> class II expression on immature ( ** P < 0.01) and mature DCs ( ** P < 0.01) was reduced by T-MSCs, <t>but</t> <t>CD14</t> expression was not affected.
Er Tr2 (Rat Anti Mouse Major Histocompatibility Complex [Mhc] Class Ii, supplied by Biozol Diagnostica Vertrieb GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


T-MSCs inhibit differentiation and maturation of DCs under coculture conditions. Bone-marrow- (BM-) derived monocytes (BMCs) isolated from 8-week-old BALB/c mice were incubated with of granulocyte-macrophage colony-stimulating factor (GM-CSF) (20 ng/mL) for 12 days to induce differentiation into dendritic cells (DCs). (a) Lipopolysaccharide (LPS) (1 μ g/mL) was added for the last 2 days to induce DC maturation. (b) GM-CSF treatment induced expansion of CD11b + cells ( ** P < 0.01). (c) Tonsil-derived MSCs (T-MSCs) added at day 0, but not at day 10, inhibited upregulated expression of CD80 ( * P < 0.05) and CD86 ( ** P < 0.01) on mature DCs by direct contact. Upregulated major histocompatibility complex (MHC) class II expression on immature ( ** P < 0.01) and mature DCs ( ** P < 0.01) was reduced by T-MSCs, but CD14 expression was not affected.

Journal: Stem Cells International

Article Title: Immune Suppressive Effects of Tonsil-Derived Mesenchymal Stem Cells on Mouse Bone-Marrow-Derived Dendritic Cells

doi: 10.1155/2015/106540

Figure Lengend Snippet: T-MSCs inhibit differentiation and maturation of DCs under coculture conditions. Bone-marrow- (BM-) derived monocytes (BMCs) isolated from 8-week-old BALB/c mice were incubated with of granulocyte-macrophage colony-stimulating factor (GM-CSF) (20 ng/mL) for 12 days to induce differentiation into dendritic cells (DCs). (a) Lipopolysaccharide (LPS) (1 μ g/mL) was added for the last 2 days to induce DC maturation. (b) GM-CSF treatment induced expansion of CD11b + cells ( ** P < 0.01). (c) Tonsil-derived MSCs (T-MSCs) added at day 0, but not at day 10, inhibited upregulated expression of CD80 ( * P < 0.05) and CD86 ( ** P < 0.01) on mature DCs by direct contact. Upregulated major histocompatibility complex (MHC) class II expression on immature ( ** P < 0.01) and mature DCs ( ** P < 0.01) was reduced by T-MSCs, but CD14 expression was not affected.

Article Snippet: For phenotyping, cells were incubated with the following fluorochrome-conjugated antibodies at final concentration of 2 ug/mL: FITC-anti-mouse CD11b (M1/70, Rat IgG 2b , eBiosciences, San Diego, CA), PE-anti-mouse CD11c (HL3, Hamster IgG 1 , BD Biosciences, Franklin Lakes, NJ), APC-anti-mouse CD11c (N418, Hamster IgG, BioLegend, San Diego, CA), PerCP-anti-mouse CD80 (16-1 OA1, Hamster IgG 2 , BD Biosciences), PE-anti-mouse CD86 (GL1, Rat IgG 2a , BD Biosciences), PE-anti-mouse CD14 (rmC5-3, Rat IgG 1 , BD Biosciences), PE-anti-mouse class II major histocompatibility complex (MHC) (2G9, Rat IgG 2a , BD Biosciences), and PE-anti-mouse CCR7 (4B12, Rat IgG 2a , R&D Systems).

Techniques: Derivative Assay, Isolation, Incubation, Expressing

T-MSCs inhibit differentiation and maturation of DCs by secretion of soluble factors. (a) BMCs and T-MSCs were cultured in a transwell plate and BMCs were induced to differentiate into DCs by GM-CSF. (b) BMCs differentiation into CD11b + cells was inhibited by T-MSCs added at day 0 ( ** P < 0.01). (c) CD86 expression on mature DCs was significantly downregulated by T-MSCs ( ** P < 0.01). Similar to the coculture condition, MHC class II expression on immature and mature DCs was inhibited by factors secreted from T-MSCs ( ** P < 0.01). CD14 expression by T-MSCs showed a trend toward increase, but it was not significant.

Journal: Stem Cells International

Article Title: Immune Suppressive Effects of Tonsil-Derived Mesenchymal Stem Cells on Mouse Bone-Marrow-Derived Dendritic Cells

doi: 10.1155/2015/106540

Figure Lengend Snippet: T-MSCs inhibit differentiation and maturation of DCs by secretion of soluble factors. (a) BMCs and T-MSCs were cultured in a transwell plate and BMCs were induced to differentiate into DCs by GM-CSF. (b) BMCs differentiation into CD11b + cells was inhibited by T-MSCs added at day 0 ( ** P < 0.01). (c) CD86 expression on mature DCs was significantly downregulated by T-MSCs ( ** P < 0.01). Similar to the coculture condition, MHC class II expression on immature and mature DCs was inhibited by factors secreted from T-MSCs ( ** P < 0.01). CD14 expression by T-MSCs showed a trend toward increase, but it was not significant.

Article Snippet: For phenotyping, cells were incubated with the following fluorochrome-conjugated antibodies at final concentration of 2 ug/mL: FITC-anti-mouse CD11b (M1/70, Rat IgG 2b , eBiosciences, San Diego, CA), PE-anti-mouse CD11c (HL3, Hamster IgG 1 , BD Biosciences, Franklin Lakes, NJ), APC-anti-mouse CD11c (N418, Hamster IgG, BioLegend, San Diego, CA), PerCP-anti-mouse CD80 (16-1 OA1, Hamster IgG 2 , BD Biosciences), PE-anti-mouse CD86 (GL1, Rat IgG 2a , BD Biosciences), PE-anti-mouse CD14 (rmC5-3, Rat IgG 1 , BD Biosciences), PE-anti-mouse class II major histocompatibility complex (MHC) (2G9, Rat IgG 2a , BD Biosciences), and PE-anti-mouse CCR7 (4B12, Rat IgG 2a , R&D Systems).

Techniques: Cell Culture, Expressing