284-2 Search Results


sk rst cell line  (ATCC)
94
ATCC sk rst cell line
Sk Rst Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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bovine leukemia virus antibody test kit»  (VMRD Inc)
93
VMRD Inc bovine leukemia virus antibody test kit»
Bovine Leukemia Virus Antibody Test Kit», supplied by VMRD Inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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phospho her3 erbb3  (Cell Signaling Technology Inc)
94
Cell Signaling Technology Inc phospho her3 erbb3
Phospho Her3 Erbb3, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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616 triethanolamine hydrochloride chem impex international  (Chem Impex International)
96
Chem Impex International 616 triethanolamine hydrochloride chem impex international
616 Triethanolamine Hydrochloride Chem Impex International, supplied by Chem Impex International, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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17 α methyltestosterone 302 46 cerilliant  (Cerilliant Corporation)
88
Cerilliant Corporation 17 α methyltestosterone 302 46 cerilliant
17 α Methyltestosterone 302 46 Cerilliant, supplied by Cerilliant Corporation, used in various techniques. Bioz Stars score: 88/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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anti bovine cd3  (VMRD Inc)
94
VMRD Inc anti bovine cd3
CD2 − natural killer (NK) cells are the predominant subset of NK cells present within skin‐draining afferent lymph (AL). Lymphocytes derived from peripheral blood (PB), AL and the lymph nodes (LNs) of seven calves were labelled with monoclonal antibodies to NKp46, <t>CD3</t> and CD2 and analysed by flow cytometry. FACS plots from one representative animal illustrate the expression of NKp46 and CD3 by PB‐, AL‐ and LN‐derived lymphocytes (a). FACS plots from one representative animal illustrate the expression of NKp46 and CD2 by PB‐, AL‐ and LN‐derived lymphocytes (b). Gates were set based on Fluorescence Minus One controls. Pooled data from seven calves indicate the average percentage of NKp46 + CD3 − NK cells ± SD present in PB (circles), AL (squares) and LNs (triangles) (c). Pooled data from seven calves illustrate the average percentage of CD2 + (lighter bars) and CD2 − (darker bars) NK cells ± SD within the total gated NKp46 + NK cell population from PB, AL or the LNs (d). Data were normally distributed ( P > 0·05). Significance between PB and AL was assessed using a paired t ‐test and significance between PB and LN was assessed using a two‐sample t ‐test. P < 0·001***. [Colour figure can be viewed at wileyonlinelibrary.com ]
Anti Bovine Cd3, supplied by VMRD Inc, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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np 284247 1  (ATCC)
93
ATCC np 284247 1
CD2 − natural killer (NK) cells are the predominant subset of NK cells present within skin‐draining afferent lymph (AL). Lymphocytes derived from peripheral blood (PB), AL and the lymph nodes (LNs) of seven calves were labelled with monoclonal antibodies to NKp46, <t>CD3</t> and CD2 and analysed by flow cytometry. FACS plots from one representative animal illustrate the expression of NKp46 and CD3 by PB‐, AL‐ and LN‐derived lymphocytes (a). FACS plots from one representative animal illustrate the expression of NKp46 and CD2 by PB‐, AL‐ and LN‐derived lymphocytes (b). Gates were set based on Fluorescence Minus One controls. Pooled data from seven calves indicate the average percentage of NKp46 + CD3 − NK cells ± SD present in PB (circles), AL (squares) and LNs (triangles) (c). Pooled data from seven calves illustrate the average percentage of CD2 + (lighter bars) and CD2 − (darker bars) NK cells ± SD within the total gated NKp46 + NK cell population from PB, AL or the LNs (d). Data were normally distributed ( P > 0·05). Significance between PB and AL was assessed using a paired t ‐test and significance between PB and LN was assessed using a two‐sample t ‐test. P < 0·001***. [Colour figure can be viewed at wileyonlinelibrary.com ]
Np 284247 1, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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hiv p24 1 control yes  (Biosynth Carbosynth)
92
Biosynth Carbosynth hiv p24 1 control yes
CD2 − natural killer (NK) cells are the predominant subset of NK cells present within skin‐draining afferent lymph (AL). Lymphocytes derived from peripheral blood (PB), AL and the lymph nodes (LNs) of seven calves were labelled with monoclonal antibodies to NKp46, <t>CD3</t> and CD2 and analysed by flow cytometry. FACS plots from one representative animal illustrate the expression of NKp46 and CD3 by PB‐, AL‐ and LN‐derived lymphocytes (a). FACS plots from one representative animal illustrate the expression of NKp46 and CD2 by PB‐, AL‐ and LN‐derived lymphocytes (b). Gates were set based on Fluorescence Minus One controls. Pooled data from seven calves indicate the average percentage of NKp46 + CD3 − NK cells ± SD present in PB (circles), AL (squares) and LNs (triangles) (c). Pooled data from seven calves illustrate the average percentage of CD2 + (lighter bars) and CD2 − (darker bars) NK cells ± SD within the total gated NKp46 + NK cell population from PB, AL or the LNs (d). Data were normally distributed ( P > 0·05). Significance between PB and AL was assessed using a paired t ‐test and significance between PB and LN was assessed using a two‐sample t ‐test. P < 0·001***. [Colour figure can be viewed at wileyonlinelibrary.com ]
Hiv P24 1 Control Yes, supplied by Biosynth Carbosynth, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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np 284268 1  (ATCC)
90
ATCC np 284268 1
CD2 − natural killer (NK) cells are the predominant subset of NK cells present within skin‐draining afferent lymph (AL). Lymphocytes derived from peripheral blood (PB), AL and the lymph nodes (LNs) of seven calves were labelled with monoclonal antibodies to NKp46, <t>CD3</t> and CD2 and analysed by flow cytometry. FACS plots from one representative animal illustrate the expression of NKp46 and CD3 by PB‐, AL‐ and LN‐derived lymphocytes (a). FACS plots from one representative animal illustrate the expression of NKp46 and CD2 by PB‐, AL‐ and LN‐derived lymphocytes (b). Gates were set based on Fluorescence Minus One controls. Pooled data from seven calves indicate the average percentage of NKp46 + CD3 − NK cells ± SD present in PB (circles), AL (squares) and LNs (triangles) (c). Pooled data from seven calves illustrate the average percentage of CD2 + (lighter bars) and CD2 − (darker bars) NK cells ± SD within the total gated NKp46 + NK cell population from PB, AL or the LNs (d). Data were normally distributed ( P > 0·05). Significance between PB and AL was assessed using a paired t ‐test and significance between PB and LN was assessed using a two‐sample t ‐test. P < 0·001***. [Colour figure can be viewed at wileyonlinelibrary.com ]
Np 284268 1, supplied by ATCC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/np 284268 1/product/ATCC
Average 90 stars, based on 1 article reviews
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acacetin (c16h12o5, cas number 480-44-4, mw 284.2, purity 98)  (ChengDu Biopurify Phytochemicals Ltd)
90
ChengDu Biopurify Phytochemicals Ltd acacetin (c16h12o5, cas number 480-44-4, mw 284.2, purity 98)
CD2 − natural killer (NK) cells are the predominant subset of NK cells present within skin‐draining afferent lymph (AL). Lymphocytes derived from peripheral blood (PB), AL and the lymph nodes (LNs) of seven calves were labelled with monoclonal antibodies to NKp46, <t>CD3</t> and CD2 and analysed by flow cytometry. FACS plots from one representative animal illustrate the expression of NKp46 and CD3 by PB‐, AL‐ and LN‐derived lymphocytes (a). FACS plots from one representative animal illustrate the expression of NKp46 and CD2 by PB‐, AL‐ and LN‐derived lymphocytes (b). Gates were set based on Fluorescence Minus One controls. Pooled data from seven calves indicate the average percentage of NKp46 + CD3 − NK cells ± SD present in PB (circles), AL (squares) and LNs (triangles) (c). Pooled data from seven calves illustrate the average percentage of CD2 + (lighter bars) and CD2 − (darker bars) NK cells ± SD within the total gated NKp46 + NK cell population from PB, AL or the LNs (d). Data were normally distributed ( P > 0·05). Significance between PB and AL was assessed using a paired t ‐test and significance between PB and LN was assessed using a two‐sample t ‐test. P < 0·001***. [Colour figure can be viewed at wileyonlinelibrary.com ]
Acacetin (C16h12o5, Cas Number 480 44 4, Mw 284.2, Purity 98), supplied by ChengDu Biopurify Phytochemicals Ltd, 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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Average 90 stars, based on 1 article reviews
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cds_1248_unigene_2842  (Unigene)
90
Unigene cds_1248_unigene_2842
CD2 − natural killer (NK) cells are the predominant subset of NK cells present within skin‐draining afferent lymph (AL). Lymphocytes derived from peripheral blood (PB), AL and the lymph nodes (LNs) of seven calves were labelled with monoclonal antibodies to NKp46, <t>CD3</t> and CD2 and analysed by flow cytometry. FACS plots from one representative animal illustrate the expression of NKp46 and CD3 by PB‐, AL‐ and LN‐derived lymphocytes (a). FACS plots from one representative animal illustrate the expression of NKp46 and CD2 by PB‐, AL‐ and LN‐derived lymphocytes (b). Gates were set based on Fluorescence Minus One controls. Pooled data from seven calves indicate the average percentage of NKp46 + CD3 − NK cells ± SD present in PB (circles), AL (squares) and LNs (triangles) (c). Pooled data from seven calves illustrate the average percentage of CD2 + (lighter bars) and CD2 − (darker bars) NK cells ± SD within the total gated NKp46 + NK cell population from PB, AL or the LNs (d). Data were normally distributed ( P > 0·05). Significance between PB and AL was assessed using a paired t ‐test and significance between PB and LN was assessed using a two‐sample t ‐test. P < 0·001***. [Colour figure can be viewed at wileyonlinelibrary.com ]
Cds 1248 Unigene 2842, supplied by Unigene, 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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compound 2842  (Trihydro Corporation)
90
Trihydro Corporation compound 2842
CD2 − natural killer (NK) cells are the predominant subset of NK cells present within skin‐draining afferent lymph (AL). Lymphocytes derived from peripheral blood (PB), AL and the lymph nodes (LNs) of seven calves were labelled with monoclonal antibodies to NKp46, <t>CD3</t> and CD2 and analysed by flow cytometry. FACS plots from one representative animal illustrate the expression of NKp46 and CD3 by PB‐, AL‐ and LN‐derived lymphocytes (a). FACS plots from one representative animal illustrate the expression of NKp46 and CD2 by PB‐, AL‐ and LN‐derived lymphocytes (b). Gates were set based on Fluorescence Minus One controls. Pooled data from seven calves indicate the average percentage of NKp46 + CD3 − NK cells ± SD present in PB (circles), AL (squares) and LNs (triangles) (c). Pooled data from seven calves illustrate the average percentage of CD2 + (lighter bars) and CD2 − (darker bars) NK cells ± SD within the total gated NKp46 + NK cell population from PB, AL or the LNs (d). Data were normally distributed ( P > 0·05). Significance between PB and AL was assessed using a paired t ‐test and significance between PB and LN was assessed using a two‐sample t ‐test. P < 0·001***. [Colour figure can be viewed at wileyonlinelibrary.com ]
Compound 2842, supplied by Trihydro Corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/compound 2842/product/Trihydro Corporation
Average 90 stars, based on 1 article reviews
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Image Search Results


CD2 − natural killer (NK) cells are the predominant subset of NK cells present within skin‐draining afferent lymph (AL). Lymphocytes derived from peripheral blood (PB), AL and the lymph nodes (LNs) of seven calves were labelled with monoclonal antibodies to NKp46, CD3 and CD2 and analysed by flow cytometry. FACS plots from one representative animal illustrate the expression of NKp46 and CD3 by PB‐, AL‐ and LN‐derived lymphocytes (a). FACS plots from one representative animal illustrate the expression of NKp46 and CD2 by PB‐, AL‐ and LN‐derived lymphocytes (b). Gates were set based on Fluorescence Minus One controls. Pooled data from seven calves indicate the average percentage of NKp46 + CD3 − NK cells ± SD present in PB (circles), AL (squares) and LNs (triangles) (c). Pooled data from seven calves illustrate the average percentage of CD2 + (lighter bars) and CD2 − (darker bars) NK cells ± SD within the total gated NKp46 + NK cell population from PB, AL or the LNs (d). Data were normally distributed ( P > 0·05). Significance between PB and AL was assessed using a paired t ‐test and significance between PB and LN was assessed using a two‐sample t ‐test. P < 0·001***. [Colour figure can be viewed at wileyonlinelibrary.com ]

Journal: Immunology

Article Title: Frequency and phenotype of natural killer cells and natural killer cell subsets in bovine lymphoid compartments and blood

doi: 10.1111/imm.12708

Figure Lengend Snippet: CD2 − natural killer (NK) cells are the predominant subset of NK cells present within skin‐draining afferent lymph (AL). Lymphocytes derived from peripheral blood (PB), AL and the lymph nodes (LNs) of seven calves were labelled with monoclonal antibodies to NKp46, CD3 and CD2 and analysed by flow cytometry. FACS plots from one representative animal illustrate the expression of NKp46 and CD3 by PB‐, AL‐ and LN‐derived lymphocytes (a). FACS plots from one representative animal illustrate the expression of NKp46 and CD2 by PB‐, AL‐ and LN‐derived lymphocytes (b). Gates were set based on Fluorescence Minus One controls. Pooled data from seven calves indicate the average percentage of NKp46 + CD3 − NK cells ± SD present in PB (circles), AL (squares) and LNs (triangles) (c). Pooled data from seven calves illustrate the average percentage of CD2 + (lighter bars) and CD2 − (darker bars) NK cells ± SD within the total gated NKp46 + NK cell population from PB, AL or the LNs (d). Data were normally distributed ( P > 0·05). Significance between PB and AL was assessed using a paired t ‐test and significance between PB and LN was assessed using a two‐sample t ‐test. P < 0·001***. [Colour figure can be viewed at wileyonlinelibrary.com ]

Article Snippet: NK cells were identified by labelling cells with mouse anti‐bovine CD3 (MM1A, IgG1, VMRD, WA) indirectly conjugated to goat anti‐mouse IgG1‐AF647 (Life Technologies, Warrington, UK), phycoerythrin‐conjugated mouse anti‐bovine CD335 (AKS1, IgG1; Bio‐Rad AbD Serotec, Kidlington, UK) or mouse anti‐bovine CD335 (AKS6, IgG2b; a gift from Professor A.K.

Techniques: Derivative Assay, Flow Cytometry, Expressing, Fluorescence

Natural killer (NK) cells are present in bovine efferent lymph and CD2 − NK cells are the principal subset present. Lymphocytes derived from peripheral blood (PB), afferent lymph (AL), lymph nodes (LNs) and efferent lymph (EL) were labelled with monoclonal antibodies for NKp46, CD3 and CD2 and analysed by flow cytometry. Pooled data from seven calves for PB, AL and LNs and five calves for EL, show the average percentage of NKp46 + CD3 − NK cells ± SD present within PB (circles), AL (squares), LNs (triangles) and EL (diamonds) (a). Pooled data from seven (PB, AL and LNs) and five (EL) calves illustrate the average percentage of NKp46 + CD2 + (lighter bars) and NKp46 + CD2 − (darker bars) NK cells ± SD within the total gated NKp46 + NK cell population from PB, AL, LNs and five calves for EL (b). Data were normally distributed ( P > 0·05) and significance between PB and EL was assessed using a two‐sample t ‐test. P < 0·01**, P < 0·001***.

Journal: Immunology

Article Title: Frequency and phenotype of natural killer cells and natural killer cell subsets in bovine lymphoid compartments and blood

doi: 10.1111/imm.12708

Figure Lengend Snippet: Natural killer (NK) cells are present in bovine efferent lymph and CD2 − NK cells are the principal subset present. Lymphocytes derived from peripheral blood (PB), afferent lymph (AL), lymph nodes (LNs) and efferent lymph (EL) were labelled with monoclonal antibodies for NKp46, CD3 and CD2 and analysed by flow cytometry. Pooled data from seven calves for PB, AL and LNs and five calves for EL, show the average percentage of NKp46 + CD3 − NK cells ± SD present within PB (circles), AL (squares), LNs (triangles) and EL (diamonds) (a). Pooled data from seven (PB, AL and LNs) and five (EL) calves illustrate the average percentage of NKp46 + CD2 + (lighter bars) and NKp46 + CD2 − (darker bars) NK cells ± SD within the total gated NKp46 + NK cell population from PB, AL, LNs and five calves for EL (b). Data were normally distributed ( P > 0·05) and significance between PB and EL was assessed using a two‐sample t ‐test. P < 0·01**, P < 0·001***.

Article Snippet: NK cells were identified by labelling cells with mouse anti‐bovine CD3 (MM1A, IgG1, VMRD, WA) indirectly conjugated to goat anti‐mouse IgG1‐AF647 (Life Technologies, Warrington, UK), phycoerythrin‐conjugated mouse anti‐bovine CD335 (AKS1, IgG1; Bio‐Rad AbD Serotec, Kidlington, UK) or mouse anti‐bovine CD335 (AKS6, IgG2b; a gift from Professor A.K.

Techniques: Derivative Assay, Flow Cytometry