d escherichia coli Search Results


91
R&D Systems escherichia coli
Escherichia Coli, supplied by R&D Systems, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/escherichia coli/product/R&D Systems
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escherichia coli - by Bioz Stars, 2026-03
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Chem Impex International n acetylneuraminic acid
N Acetylneuraminic Acid, supplied by Chem Impex International, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/n acetylneuraminic acid/product/Chem Impex International
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Cusabio recombinant escherichia coli type 1 fimbrin dmannose specific adhesin fimh
Recombinant Escherichia Coli Type 1 Fimbrin Dmannose Specific Adhesin Fimh, supplied by Cusabio, 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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Harlan Laboratories salmonella typhimurium and escherichia coli reverse mutation assay with menthone-l / isomenthone-d
Salmonella Typhimurium And Escherichia Coli Reverse Mutation Assay With Menthone L / Isomenthone D, supplied by Harlan Laboratories, 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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Intervet International GmbH bovine rotavirus-coronavirus vaccine- clostridium perfringens types c and d- escherichia coli bacterin-toxoid
Licensed veterinary biological products containing bacterins, bacterial extracts, and/or toxoids approved for use in cattle
Bovine Rotavirus Coronavirus Vaccine Clostridium Perfringens Types C And D Escherichia Coli Bacterin Toxoid, supplied by Intervet International GmbH, 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/bovine rotavirus-coronavirus vaccine- clostridium perfringens types c and d- escherichia coli bacterin-toxoid/product/Intervet International GmbH
Average 90 stars, based on 1 article reviews
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90
Proimmune pe-conjugated h-2l d tetramer to peptide tphparigl (escherichia coli β-galactosidase 876–884)
T reg cell inhibition by OX40 triggering allows TIDC maturation and priming of new CTLs. (A) Rescue of DC migration after T reg cell inhibition. FITC-conjugated latex particles (2 × 10 7 beads) of 1 μm in diameter were coinjected with anti-OX40, anti-CD25, or rat IgG (mock) within tumors of 3–4 mm in diameter. After 24 h, axillary and inguinal draining lymph nodes were collected and treated with collagenase D, and the obtained cell suspensions were stained for CD11c. The number of CD11c + cells showing green fluorescence because of microbead engulfment was evaluated by flow cytometry. Each symbol corresponds to a single draining lymph node; the solid line represents the median value. Results are a pooled representation of three independent experiments. *, P < 0.05. (B) Induction of tumor-specific CD8 + T lymphocytes. (top) Tumor-bearing mice received intratumor injection of anti-CD25, anti-OX40, or rat IgG (mock). 5 d after treatment, axillary and inguinal draining lymph nodes were collected and stained for flow cytometry. On gated CD8 + T cells, the percentage of tumor-specific clones was evaluated by staining with H2L d tetramers recognizing the SPSYVYHQF peptide of the gp70-env tumor-associated antigen. As a background staining, H2L d tetramers specific for the unrelated peptide <t>TPHPARIGL</t> ( E. coli β-galactosidase 876–884) were used. Percentages of tumor-specific CD8 + T cells were calculated by subtracting the background (β-galactosidase) from the specific (gp70-env) staining. OX86-treated mice showed the highest percentage of tumor-specific CD8 + T cells in the draining lymph nodes. Each symbol represents the draining lymph node of randomly chosen mice from two independent experiments. The solid line represents the median value. *, P < 0.05. (bottom) Representative histograms of tetramer-stained cells gated on CD8 + T cells are shown (indicated as percentages). Gp70-H2L d tetramer staining (continuous line) was overlaid with β-galactosidase–H2L d control tetramer staining (shaded line). The subtracted value is indicated for each sample. (insets) Surface expression of the T cell memory marker CD44 on gp70-H2L d tetramer–positive CD8 + T cells.
Pe Conjugated H 2l D Tetramer To Peptide Tphparigl (Escherichia Coli β Galactosidase 876–884), supplied by Proimmune, 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/pe-conjugated h-2l d tetramer to peptide tphparigl (escherichia coli β-galactosidase 876–884)/product/Proimmune
Average 90 stars, based on 1 article reviews
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90
Fluka Chemical d-aminoacylase from escherichia. coli
T reg cell inhibition by OX40 triggering allows TIDC maturation and priming of new CTLs. (A) Rescue of DC migration after T reg cell inhibition. FITC-conjugated latex particles (2 × 10 7 beads) of 1 μm in diameter were coinjected with anti-OX40, anti-CD25, or rat IgG (mock) within tumors of 3–4 mm in diameter. After 24 h, axillary and inguinal draining lymph nodes were collected and treated with collagenase D, and the obtained cell suspensions were stained for CD11c. The number of CD11c + cells showing green fluorescence because of microbead engulfment was evaluated by flow cytometry. Each symbol corresponds to a single draining lymph node; the solid line represents the median value. Results are a pooled representation of three independent experiments. *, P < 0.05. (B) Induction of tumor-specific CD8 + T lymphocytes. (top) Tumor-bearing mice received intratumor injection of anti-CD25, anti-OX40, or rat IgG (mock). 5 d after treatment, axillary and inguinal draining lymph nodes were collected and stained for flow cytometry. On gated CD8 + T cells, the percentage of tumor-specific clones was evaluated by staining with H2L d tetramers recognizing the SPSYVYHQF peptide of the gp70-env tumor-associated antigen. As a background staining, H2L d tetramers specific for the unrelated peptide <t>TPHPARIGL</t> ( E. coli β-galactosidase 876–884) were used. Percentages of tumor-specific CD8 + T cells were calculated by subtracting the background (β-galactosidase) from the specific (gp70-env) staining. OX86-treated mice showed the highest percentage of tumor-specific CD8 + T cells in the draining lymph nodes. Each symbol represents the draining lymph node of randomly chosen mice from two independent experiments. The solid line represents the median value. *, P < 0.05. (bottom) Representative histograms of tetramer-stained cells gated on CD8 + T cells are shown (indicated as percentages). Gp70-H2L d tetramer staining (continuous line) was overlaid with β-galactosidase–H2L d control tetramer staining (shaded line). The subtracted value is indicated for each sample. (insets) Surface expression of the T cell memory marker CD44 on gp70-H2L d tetramer–positive CD8 + T cells.
D Aminoacylase From Escherichia. Coli, supplied by Fluka Chemical, 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/d-aminoacylase from escherichia. coli/product/Fluka Chemical
Average 90 stars, based on 1 article reviews
d-aminoacylase from escherichia. coli - by Bioz Stars, 2026-03
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Wulff labs d-aminolevulic acid-requiring mutant of escherichia coli
T reg cell inhibition by OX40 triggering allows TIDC maturation and priming of new CTLs. (A) Rescue of DC migration after T reg cell inhibition. FITC-conjugated latex particles (2 × 10 7 beads) of 1 μm in diameter were coinjected with anti-OX40, anti-CD25, or rat IgG (mock) within tumors of 3–4 mm in diameter. After 24 h, axillary and inguinal draining lymph nodes were collected and treated with collagenase D, and the obtained cell suspensions were stained for CD11c. The number of CD11c + cells showing green fluorescence because of microbead engulfment was evaluated by flow cytometry. Each symbol corresponds to a single draining lymph node; the solid line represents the median value. Results are a pooled representation of three independent experiments. *, P < 0.05. (B) Induction of tumor-specific CD8 + T lymphocytes. (top) Tumor-bearing mice received intratumor injection of anti-CD25, anti-OX40, or rat IgG (mock). 5 d after treatment, axillary and inguinal draining lymph nodes were collected and stained for flow cytometry. On gated CD8 + T cells, the percentage of tumor-specific clones was evaluated by staining with H2L d tetramers recognizing the SPSYVYHQF peptide of the gp70-env tumor-associated antigen. As a background staining, H2L d tetramers specific for the unrelated peptide <t>TPHPARIGL</t> ( E. coli β-galactosidase 876–884) were used. Percentages of tumor-specific CD8 + T cells were calculated by subtracting the background (β-galactosidase) from the specific (gp70-env) staining. OX86-treated mice showed the highest percentage of tumor-specific CD8 + T cells in the draining lymph nodes. Each symbol represents the draining lymph node of randomly chosen mice from two independent experiments. The solid line represents the median value. *, P < 0.05. (bottom) Representative histograms of tetramer-stained cells gated on CD8 + T cells are shown (indicated as percentages). Gp70-H2L d tetramer staining (continuous line) was overlaid with β-galactosidase–H2L d control tetramer staining (shaded line). The subtracted value is indicated for each sample. (insets) Surface expression of the T cell memory marker CD44 on gp70-H2L d tetramer–positive CD8 + T cells.
D Aminolevulic Acid Requiring Mutant Of Escherichia Coli, supplied by Wulff labs, 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/d-aminolevulic acid-requiring mutant of escherichia coli/product/Wulff labs
Average 90 stars, based on 1 article reviews
d-aminolevulic acid-requiring mutant of escherichia coli - by Bioz Stars, 2026-03
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90
Boehringer Mannheim fi-d-galactosidase from escherichia coli
T reg cell inhibition by OX40 triggering allows TIDC maturation and priming of new CTLs. (A) Rescue of DC migration after T reg cell inhibition. FITC-conjugated latex particles (2 × 10 7 beads) of 1 μm in diameter were coinjected with anti-OX40, anti-CD25, or rat IgG (mock) within tumors of 3–4 mm in diameter. After 24 h, axillary and inguinal draining lymph nodes were collected and treated with collagenase D, and the obtained cell suspensions were stained for CD11c. The number of CD11c + cells showing green fluorescence because of microbead engulfment was evaluated by flow cytometry. Each symbol corresponds to a single draining lymph node; the solid line represents the median value. Results are a pooled representation of three independent experiments. *, P < 0.05. (B) Induction of tumor-specific CD8 + T lymphocytes. (top) Tumor-bearing mice received intratumor injection of anti-CD25, anti-OX40, or rat IgG (mock). 5 d after treatment, axillary and inguinal draining lymph nodes were collected and stained for flow cytometry. On gated CD8 + T cells, the percentage of tumor-specific clones was evaluated by staining with H2L d tetramers recognizing the SPSYVYHQF peptide of the gp70-env tumor-associated antigen. As a background staining, H2L d tetramers specific for the unrelated peptide <t>TPHPARIGL</t> ( E. coli β-galactosidase 876–884) were used. Percentages of tumor-specific CD8 + T cells were calculated by subtracting the background (β-galactosidase) from the specific (gp70-env) staining. OX86-treated mice showed the highest percentage of tumor-specific CD8 + T cells in the draining lymph nodes. Each symbol represents the draining lymph node of randomly chosen mice from two independent experiments. The solid line represents the median value. *, P < 0.05. (bottom) Representative histograms of tetramer-stained cells gated on CD8 + T cells are shown (indicated as percentages). Gp70-H2L d tetramer staining (continuous line) was overlaid with β-galactosidase–H2L d control tetramer staining (shaded line). The subtracted value is indicated for each sample. (insets) Surface expression of the T cell memory marker CD44 on gp70-H2L d tetramer–positive CD8 + T cells.
Fi D Galactosidase From Escherichia Coli, supplied by Boehringer Mannheim, 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/fi-d-galactosidase from escherichia coli/product/Boehringer Mannheim
Average 90 stars, based on 1 article reviews
fi-d-galactosidase from escherichia coli - by Bioz Stars, 2026-03
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90
Sandoz escherichia coli strain d 120
T reg cell inhibition by OX40 triggering allows TIDC maturation and priming of new CTLs. (A) Rescue of DC migration after T reg cell inhibition. FITC-conjugated latex particles (2 × 10 7 beads) of 1 μm in diameter were coinjected with anti-OX40, anti-CD25, or rat IgG (mock) within tumors of 3–4 mm in diameter. After 24 h, axillary and inguinal draining lymph nodes were collected and treated with collagenase D, and the obtained cell suspensions were stained for CD11c. The number of CD11c + cells showing green fluorescence because of microbead engulfment was evaluated by flow cytometry. Each symbol corresponds to a single draining lymph node; the solid line represents the median value. Results are a pooled representation of three independent experiments. *, P < 0.05. (B) Induction of tumor-specific CD8 + T lymphocytes. (top) Tumor-bearing mice received intratumor injection of anti-CD25, anti-OX40, or rat IgG (mock). 5 d after treatment, axillary and inguinal draining lymph nodes were collected and stained for flow cytometry. On gated CD8 + T cells, the percentage of tumor-specific clones was evaluated by staining with H2L d tetramers recognizing the SPSYVYHQF peptide of the gp70-env tumor-associated antigen. As a background staining, H2L d tetramers specific for the unrelated peptide <t>TPHPARIGL</t> ( E. coli β-galactosidase 876–884) were used. Percentages of tumor-specific CD8 + T cells were calculated by subtracting the background (β-galactosidase) from the specific (gp70-env) staining. OX86-treated mice showed the highest percentage of tumor-specific CD8 + T cells in the draining lymph nodes. Each symbol represents the draining lymph node of randomly chosen mice from two independent experiments. The solid line represents the median value. *, P < 0.05. (bottom) Representative histograms of tetramer-stained cells gated on CD8 + T cells are shown (indicated as percentages). Gp70-H2L d tetramer staining (continuous line) was overlaid with β-galactosidase–H2L d control tetramer staining (shaded line). The subtracted value is indicated for each sample. (insets) Surface expression of the T cell memory marker CD44 on gp70-H2L d tetramer–positive CD8 + T cells.
Escherichia Coli Strain D 120, supplied by Sandoz, 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/escherichia coli strain d 120/product/Sandoz
Average 90 stars, based on 1 article reviews
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90
Pfizer Animal Health transmissible gastroenteritis, clostridium perfringens type c, escherichia coli bacterin toxoid scourshield d
T reg cell inhibition by OX40 triggering allows TIDC maturation and priming of new CTLs. (A) Rescue of DC migration after T reg cell inhibition. FITC-conjugated latex particles (2 × 10 7 beads) of 1 μm in diameter were coinjected with anti-OX40, anti-CD25, or rat IgG (mock) within tumors of 3–4 mm in diameter. After 24 h, axillary and inguinal draining lymph nodes were collected and treated with collagenase D, and the obtained cell suspensions were stained for CD11c. The number of CD11c + cells showing green fluorescence because of microbead engulfment was evaluated by flow cytometry. Each symbol corresponds to a single draining lymph node; the solid line represents the median value. Results are a pooled representation of three independent experiments. *, P < 0.05. (B) Induction of tumor-specific CD8 + T lymphocytes. (top) Tumor-bearing mice received intratumor injection of anti-CD25, anti-OX40, or rat IgG (mock). 5 d after treatment, axillary and inguinal draining lymph nodes were collected and stained for flow cytometry. On gated CD8 + T cells, the percentage of tumor-specific clones was evaluated by staining with H2L d tetramers recognizing the SPSYVYHQF peptide of the gp70-env tumor-associated antigen. As a background staining, H2L d tetramers specific for the unrelated peptide <t>TPHPARIGL</t> ( E. coli β-galactosidase 876–884) were used. Percentages of tumor-specific CD8 + T cells were calculated by subtracting the background (β-galactosidase) from the specific (gp70-env) staining. OX86-treated mice showed the highest percentage of tumor-specific CD8 + T cells in the draining lymph nodes. Each symbol represents the draining lymph node of randomly chosen mice from two independent experiments. The solid line represents the median value. *, P < 0.05. (bottom) Representative histograms of tetramer-stained cells gated on CD8 + T cells are shown (indicated as percentages). Gp70-H2L d tetramer staining (continuous line) was overlaid with β-galactosidase–H2L d control tetramer staining (shaded line). The subtracted value is indicated for each sample. (insets) Surface expression of the T cell memory marker CD44 on gp70-H2L d tetramer–positive CD8 + T cells.
Transmissible Gastroenteritis, Clostridium Perfringens Type C, Escherichia Coli Bacterin Toxoid Scourshield D, supplied by Pfizer Animal Health, 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/transmissible gastroenteritis, clostridium perfringens type c, escherichia coli bacterin toxoid scourshield d/product/Pfizer Animal Health
Average 90 stars, based on 1 article reviews
transmissible gastroenteritis, clostridium perfringens type c, escherichia coli bacterin toxoid scourshield d - by Bioz Stars, 2026-03
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90
Bacto Laboratories escherichia coli (ec) broth containing 4-methylumbelliferyl-b-d-glucuronide
T reg cell inhibition by OX40 triggering allows TIDC maturation and priming of new CTLs. (A) Rescue of DC migration after T reg cell inhibition. FITC-conjugated latex particles (2 × 10 7 beads) of 1 μm in diameter were coinjected with anti-OX40, anti-CD25, or rat IgG (mock) within tumors of 3–4 mm in diameter. After 24 h, axillary and inguinal draining lymph nodes were collected and treated with collagenase D, and the obtained cell suspensions were stained for CD11c. The number of CD11c + cells showing green fluorescence because of microbead engulfment was evaluated by flow cytometry. Each symbol corresponds to a single draining lymph node; the solid line represents the median value. Results are a pooled representation of three independent experiments. *, P < 0.05. (B) Induction of tumor-specific CD8 + T lymphocytes. (top) Tumor-bearing mice received intratumor injection of anti-CD25, anti-OX40, or rat IgG (mock). 5 d after treatment, axillary and inguinal draining lymph nodes were collected and stained for flow cytometry. On gated CD8 + T cells, the percentage of tumor-specific clones was evaluated by staining with H2L d tetramers recognizing the SPSYVYHQF peptide of the gp70-env tumor-associated antigen. As a background staining, H2L d tetramers specific for the unrelated peptide <t>TPHPARIGL</t> ( E. coli β-galactosidase 876–884) were used. Percentages of tumor-specific CD8 + T cells were calculated by subtracting the background (β-galactosidase) from the specific (gp70-env) staining. OX86-treated mice showed the highest percentage of tumor-specific CD8 + T cells in the draining lymph nodes. Each symbol represents the draining lymph node of randomly chosen mice from two independent experiments. The solid line represents the median value. *, P < 0.05. (bottom) Representative histograms of tetramer-stained cells gated on CD8 + T cells are shown (indicated as percentages). Gp70-H2L d tetramer staining (continuous line) was overlaid with β-galactosidase–H2L d control tetramer staining (shaded line). The subtracted value is indicated for each sample. (insets) Surface expression of the T cell memory marker CD44 on gp70-H2L d tetramer–positive CD8 + T cells.
Escherichia Coli (Ec) Broth Containing 4 Methylumbelliferyl B D Glucuronide, supplied by Bacto Laboratories, 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/escherichia coli (ec) broth containing 4-methylumbelliferyl-b-d-glucuronide/product/Bacto Laboratories
Average 90 stars, based on 1 article reviews
escherichia coli (ec) broth containing 4-methylumbelliferyl-b-d-glucuronide - by Bioz Stars, 2026-03
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Image Search Results


Licensed veterinary biological products containing bacterins, bacterial extracts, and/or toxoids approved for use in cattle

Journal: The Veterinary Clinics of North America. Food Animal Practice

Article Title: Vaccination Management of Beef Cattle

doi: 10.1016/j.cvfa.2019.07.003

Figure Lengend Snippet: Licensed veterinary biological products containing bacterins, bacterial extracts, and/or toxoids approved for use in cattle

Article Snippet: Bovine rotavirus-coronavirus vaccine- Clostridium perfringens types C and D- Escherichia coli bacterin-toxoid , Intervet.

Techniques: Virus, Vaccines

T reg cell inhibition by OX40 triggering allows TIDC maturation and priming of new CTLs. (A) Rescue of DC migration after T reg cell inhibition. FITC-conjugated latex particles (2 × 10 7 beads) of 1 μm in diameter were coinjected with anti-OX40, anti-CD25, or rat IgG (mock) within tumors of 3–4 mm in diameter. After 24 h, axillary and inguinal draining lymph nodes were collected and treated with collagenase D, and the obtained cell suspensions were stained for CD11c. The number of CD11c + cells showing green fluorescence because of microbead engulfment was evaluated by flow cytometry. Each symbol corresponds to a single draining lymph node; the solid line represents the median value. Results are a pooled representation of three independent experiments. *, P < 0.05. (B) Induction of tumor-specific CD8 + T lymphocytes. (top) Tumor-bearing mice received intratumor injection of anti-CD25, anti-OX40, or rat IgG (mock). 5 d after treatment, axillary and inguinal draining lymph nodes were collected and stained for flow cytometry. On gated CD8 + T cells, the percentage of tumor-specific clones was evaluated by staining with H2L d tetramers recognizing the SPSYVYHQF peptide of the gp70-env tumor-associated antigen. As a background staining, H2L d tetramers specific for the unrelated peptide TPHPARIGL ( E. coli β-galactosidase 876–884) were used. Percentages of tumor-specific CD8 + T cells were calculated by subtracting the background (β-galactosidase) from the specific (gp70-env) staining. OX86-treated mice showed the highest percentage of tumor-specific CD8 + T cells in the draining lymph nodes. Each symbol represents the draining lymph node of randomly chosen mice from two independent experiments. The solid line represents the median value. *, P < 0.05. (bottom) Representative histograms of tetramer-stained cells gated on CD8 + T cells are shown (indicated as percentages). Gp70-H2L d tetramer staining (continuous line) was overlaid with β-galactosidase–H2L d control tetramer staining (shaded line). The subtracted value is indicated for each sample. (insets) Surface expression of the T cell memory marker CD44 on gp70-H2L d tetramer–positive CD8 + T cells.

Journal: The Journal of Experimental Medicine

Article Title: OX40 triggering blocks suppression by regulatory T cells and facilitates tumor rejection

doi: 10.1084/jem.20071341

Figure Lengend Snippet: T reg cell inhibition by OX40 triggering allows TIDC maturation and priming of new CTLs. (A) Rescue of DC migration after T reg cell inhibition. FITC-conjugated latex particles (2 × 10 7 beads) of 1 μm in diameter were coinjected with anti-OX40, anti-CD25, or rat IgG (mock) within tumors of 3–4 mm in diameter. After 24 h, axillary and inguinal draining lymph nodes were collected and treated with collagenase D, and the obtained cell suspensions were stained for CD11c. The number of CD11c + cells showing green fluorescence because of microbead engulfment was evaluated by flow cytometry. Each symbol corresponds to a single draining lymph node; the solid line represents the median value. Results are a pooled representation of three independent experiments. *, P < 0.05. (B) Induction of tumor-specific CD8 + T lymphocytes. (top) Tumor-bearing mice received intratumor injection of anti-CD25, anti-OX40, or rat IgG (mock). 5 d after treatment, axillary and inguinal draining lymph nodes were collected and stained for flow cytometry. On gated CD8 + T cells, the percentage of tumor-specific clones was evaluated by staining with H2L d tetramers recognizing the SPSYVYHQF peptide of the gp70-env tumor-associated antigen. As a background staining, H2L d tetramers specific for the unrelated peptide TPHPARIGL ( E. coli β-galactosidase 876–884) were used. Percentages of tumor-specific CD8 + T cells were calculated by subtracting the background (β-galactosidase) from the specific (gp70-env) staining. OX86-treated mice showed the highest percentage of tumor-specific CD8 + T cells in the draining lymph nodes. Each symbol represents the draining lymph node of randomly chosen mice from two independent experiments. The solid line represents the median value. *, P < 0.05. (bottom) Representative histograms of tetramer-stained cells gated on CD8 + T cells are shown (indicated as percentages). Gp70-H2L d tetramer staining (continuous line) was overlaid with β-galactosidase–H2L d control tetramer staining (shaded line). The subtracted value is indicated for each sample. (insets) Surface expression of the T cell memory marker CD44 on gp70-H2L d tetramer–positive CD8 + T cells.

Article Snippet: PE-conjugated H-2L d tetramer to peptide SPSYVYHQF (MuLV env gp70 423–431) and PE-conjugated H-2L d tetramer to peptide TPHPARIGL ( Escherichia coli β-galactosidase 876–884) were purchased from Proimmune.

Techniques: Inhibition, Migration, Staining, Fluorescence, Flow Cytometry, Injection, Clone Assay, Control, Expressing, Marker