44718 Search Results


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R&D Systems cross species reactive anti human cxcr4 monoclonal antibodies
<t>CXCR4</t> expression on feline PBMC. (A) Discrimination of lymphocytes (L), monocytes (M), and granulocytes (G) by FSC versus 90° SSC. CXCR4+ (B), CD14+ (C), and B220+ (D) cells were back gated on a plot of FSC versus SSC. The results of a two-color analysis of CXCR4 expression (phycoerythrin [PE]) versus CD14 (E), B220 (F), or CD5 (G) coupled to fluorescein isothiocyanate (FITC) is shown. Each panel represents 10,000 events. Data were analyzed with Expo ADC software (Applied Cytometry Systems, Sheffield, United Kingdom).
Cross Species Reactive Anti Human Cxcr4 Monoclonal Antibodies, supplied by R&D Systems, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/cross species reactive anti human cxcr4 monoclonal antibodies/product/R&D Systems
Average 92 stars, based on 1 article reviews
cross species reactive anti human cxcr4 monoclonal antibodies - by Bioz Stars, 2026-02
92/100 stars
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Gene Silencers generally consist of pools of three to five target specific 19 25 nucleotide sequences in length For independent verification of selenocysteine lyase gene silencing results individual duplex components or plasmids are also available
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Gene Silencers generally consist of pools of three to five target specific 19 25 nucleotide sequences in length For independent verification of selenocysteine lyase gene silencing results individual duplex components or plasmids are also available
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ENaC beta Antibody ATTO 700 is a Rabbit Polyclonal against ENaC
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Lenti ORF particles SPICE1 mGFP tagged Human spindle and centriole associated protein 1 SPICE1 200ul 10 7 TU mL
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Rabbit Polyclonal Anti HAPLN2 Antibody middle region
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Standard format Plasmid sent in bacteria as agar stab
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An ampoule containing viable cells (may include spores and mycelia) suspended in cryoprotectant.
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Lenti ORF clone of Human spindle and centriole associated protein 1 SPICE1 mGFP tagged
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ENaC beta Antibody ATTO 594 is a Rabbit Polyclonal against ENaC
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Image Search Results


CXCR4 expression on feline PBMC. (A) Discrimination of lymphocytes (L), monocytes (M), and granulocytes (G) by FSC versus 90° SSC. CXCR4+ (B), CD14+ (C), and B220+ (D) cells were back gated on a plot of FSC versus SSC. The results of a two-color analysis of CXCR4 expression (phycoerythrin [PE]) versus CD14 (E), B220 (F), or CD5 (G) coupled to fluorescein isothiocyanate (FITC) is shown. Each panel represents 10,000 events. Data were analyzed with Expo ADC software (Applied Cytometry Systems, Sheffield, United Kingdom).

Journal:

Article Title: Expression of CXCR4 on Feline Peripheral Blood Mononuclear Cells: Effect of Feline Immunodeficiency Virus Infection

doi: 10.1128/JVI.77.1.709-712.2003

Figure Lengend Snippet: CXCR4 expression on feline PBMC. (A) Discrimination of lymphocytes (L), monocytes (M), and granulocytes (G) by FSC versus 90° SSC. CXCR4+ (B), CD14+ (C), and B220+ (D) cells were back gated on a plot of FSC versus SSC. The results of a two-color analysis of CXCR4 expression (phycoerythrin [PE]) versus CD14 (E), B220 (F), or CD5 (G) coupled to fluorescein isothiocyanate (FITC) is shown. Each panel represents 10,000 events. Data were analyzed with Expo ADC software (Applied Cytometry Systems, Sheffield, United Kingdom).

Article Snippet: We used cross-species-reactive anti-human CXCR4 monoclonal antibodies (44701, 44717, and 44718; provided by M. Tsang, R&D Systems, Minneapolis, Minn.) that we identified previously ( 11 ) and two-color flow cytometry to examine CXCR4 expression on feline peripheral blood mononuclear cells (PBMC) (Fig. ).

Techniques: Expressing, Software, Cytometry

Comparison of CXCR4 expression on feline T cells with that on human T cells. Feline and human PBMC were processed for flow cytometry by whole-blood lysis. Lymphocytes were identified on the basis of FSC versus 90° SSC characteristics (dotted lines illustrate the respective sizes of feline [A] and human [D] lymphocytes, and the ellipse delineates the analysis gate). The results of a two-color analysis of CXCR4 expression (phycoerythrin [PE]) versus B220 (B) and CD5 (C) on feline lymphocytes and CD19 (E) and CD3 (F) on human lymphocytes is shown. Each panel represents 10,000 events. Data are presented with no baseline offset. FITC, fluorescein isothiocyanate.

Journal:

Article Title: Expression of CXCR4 on Feline Peripheral Blood Mononuclear Cells: Effect of Feline Immunodeficiency Virus Infection

doi: 10.1128/JVI.77.1.709-712.2003

Figure Lengend Snippet: Comparison of CXCR4 expression on feline T cells with that on human T cells. Feline and human PBMC were processed for flow cytometry by whole-blood lysis. Lymphocytes were identified on the basis of FSC versus 90° SSC characteristics (dotted lines illustrate the respective sizes of feline [A] and human [D] lymphocytes, and the ellipse delineates the analysis gate). The results of a two-color analysis of CXCR4 expression (phycoerythrin [PE]) versus B220 (B) and CD5 (C) on feline lymphocytes and CD19 (E) and CD3 (F) on human lymphocytes is shown. Each panel represents 10,000 events. Data are presented with no baseline offset. FITC, fluorescein isothiocyanate.

Article Snippet: We used cross-species-reactive anti-human CXCR4 monoclonal antibodies (44701, 44717, and 44718; provided by M. Tsang, R&D Systems, Minneapolis, Minn.) that we identified previously ( 11 ) and two-color flow cytometry to examine CXCR4 expression on feline peripheral blood mononuclear cells (PBMC) (Fig. ).

Techniques: Comparison, Expressing, Flow Cytometry, Lysis

 CXCR4  expression on monocytes, B cells, and T cells in the domestic cat a

Journal:

Article Title: Expression of CXCR4 on Feline Peripheral Blood Mononuclear Cells: Effect of Feline Immunodeficiency Virus Infection

doi: 10.1128/JVI.77.1.709-712.2003

Figure Lengend Snippet: CXCR4 expression on monocytes, B cells, and T cells in the domestic cat a

Article Snippet: We used cross-species-reactive anti-human CXCR4 monoclonal antibodies (44701, 44717, and 44718; provided by M. Tsang, R&D Systems, Minneapolis, Minn.) that we identified previously ( 11 ) and two-color flow cytometry to examine CXCR4 expression on feline peripheral blood mononuclear cells (PBMC) (Fig. ).

Techniques: Expressing, Control, Infection