endogenous streptavidin biotin binding sites Search Results


streptavidin biotin  (Agilent technologies)
99
Agilent technologies streptavidin biotin
Streptavidin Biotin, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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streptavidin biotin peroxidase system  (Vector Laboratories)
99
Vector Laboratories streptavidin biotin peroxidase system
Streptavidin Biotin Peroxidase System, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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antistreptavidin biotinylated antibody  (Vector Laboratories)
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Vector Laboratories antistreptavidin biotinylated antibody
Antistreptavidin Biotinylated Antibody, supplied by Vector Laboratories, 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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multi-link super sensitive detection system 4plus universal hpr detection system  (Biocare Medical)
90
Biocare Medical multi-link super sensitive detection system 4plus universal hpr detection system
Multi Link Super Sensitive Detection System 4plus Universal Hpr Detection System, supplied by Biocare Medical, 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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biotin  (Vector Laboratories)
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Vector Laboratories biotin
Biotin, supplied by Vector Laboratories, 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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biotinylated cd31  (Santa Cruz Biotechnology)
94
Santa Cruz Biotechnology biotinylated cd31
FIG. 2. Density distribution of common lung cell lineages. (A) Fractionated cells from sham or 2-day bleomycin-treated mice were subjected to flow cytometry and average percent of cells ( – SEM) per fraction are presented. P-value represen- tations shown: normal font—differences in the proportion of protein-expressing cells isolated between fractions from the homeostatic lung; bold font—differences in the proportion of protein-expressing cells between fractions postbleomycin treatment, and italics—overall differences in the proportion of protein-expressing cells between pre- and postbleomycin treatment regardless of fraction. No statistically significant differences were observed in the proportion of CD45-, <t>CD31-,</t> and EpCAM-positive cells between the density fractions in the homeostatic lung. In contrast, cells positive for c-KIT and CD49f were more prevalent in the lower fractions, while SCA-1 expressing cells equilibrated largely in the intermediate fractions. At day 2 following bleomycin treatment, only CD45-positive cells showed significant differences among the fractions equili- brating at the highest density (n ‡ 7; P = 0.01). (B) Representative western blots depicting levels of protein expression per fraction (n ‡ 4). The fibroblastic, smooth muscle, a1-actin (ACTA1) protein signal is highest in fractions 3 and 4 (P < 0.01 by densitometry). Levels of the epithelial (pro-) surfactant protein-C (SFTPC) and secretoglobin family 1A member 1 (SCGB1A1) protein bands are statistically significant between the fractions (P < 0.001 for both). Levels of the AT1 epithelial protein, aquaporin-5 (AQP5) are highest in the lighter fractions (P < 0.001). Bands representing levels of the endothelial CD31 protein and b-actin are also shown.
Biotinylated Cd31, supplied by Santa Cruz Biotechnology, 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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biotinylated peptides  (New England Biolabs)
97
New England Biolabs biotinylated peptides
FIG. 2. Density distribution of common lung cell lineages. (A) Fractionated cells from sham or 2-day bleomycin-treated mice were subjected to flow cytometry and average percent of cells ( – SEM) per fraction are presented. P-value represen- tations shown: normal font—differences in the proportion of protein-expressing cells isolated between fractions from the homeostatic lung; bold font—differences in the proportion of protein-expressing cells between fractions postbleomycin treatment, and italics—overall differences in the proportion of protein-expressing cells between pre- and postbleomycin treatment regardless of fraction. No statistically significant differences were observed in the proportion of CD45-, <t>CD31-,</t> and EpCAM-positive cells between the density fractions in the homeostatic lung. In contrast, cells positive for c-KIT and CD49f were more prevalent in the lower fractions, while SCA-1 expressing cells equilibrated largely in the intermediate fractions. At day 2 following bleomycin treatment, only CD45-positive cells showed significant differences among the fractions equili- brating at the highest density (n ‡ 7; P = 0.01). (B) Representative western blots depicting levels of protein expression per fraction (n ‡ 4). The fibroblastic, smooth muscle, a1-actin (ACTA1) protein signal is highest in fractions 3 and 4 (P < 0.01 by densitometry). Levels of the epithelial (pro-) surfactant protein-C (SFTPC) and secretoglobin family 1A member 1 (SCGB1A1) protein bands are statistically significant between the fractions (P < 0.001 for both). Levels of the AT1 epithelial protein, aquaporin-5 (AQP5) are highest in the lighter fractions (P < 0.001). Bands representing levels of the endothelial CD31 protein and b-actin are also shown.
Biotinylated Peptides, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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streptavidin agarose resin  (Thermo Fisher)
90
Thermo Fisher streptavidin agarose resin
FIG. 2. Density distribution of common lung cell lineages. (A) Fractionated cells from sham or 2-day bleomycin-treated mice were subjected to flow cytometry and average percent of cells ( – SEM) per fraction are presented. P-value represen- tations shown: normal font—differences in the proportion of protein-expressing cells isolated between fractions from the homeostatic lung; bold font—differences in the proportion of protein-expressing cells between fractions postbleomycin treatment, and italics—overall differences in the proportion of protein-expressing cells between pre- and postbleomycin treatment regardless of fraction. No statistically significant differences were observed in the proportion of CD45-, <t>CD31-,</t> and EpCAM-positive cells between the density fractions in the homeostatic lung. In contrast, cells positive for c-KIT and CD49f were more prevalent in the lower fractions, while SCA-1 expressing cells equilibrated largely in the intermediate fractions. At day 2 following bleomycin treatment, only CD45-positive cells showed significant differences among the fractions equili- brating at the highest density (n ‡ 7; P = 0.01). (B) Representative western blots depicting levels of protein expression per fraction (n ‡ 4). The fibroblastic, smooth muscle, a1-actin (ACTA1) protein signal is highest in fractions 3 and 4 (P < 0.01 by densitometry). Levels of the epithelial (pro-) surfactant protein-C (SFTPC) and secretoglobin family 1A member 1 (SCGB1A1) protein bands are statistically significant between the fractions (P < 0.001 for both). Levels of the AT1 epithelial protein, aquaporin-5 (AQP5) are highest in the lighter fractions (P < 0.001). Bands representing levels of the endothelial CD31 protein and b-actin are also shown.
Streptavidin Agarose Resin, supplied by Thermo Fisher, 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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labeled streptavidin biotin staining kit  (Biogenex)
90
Biogenex labeled streptavidin biotin staining kit
FIG. 2. Density distribution of common lung cell lineages. (A) Fractionated cells from sham or 2-day bleomycin-treated mice were subjected to flow cytometry and average percent of cells ( – SEM) per fraction are presented. P-value represen- tations shown: normal font—differences in the proportion of protein-expressing cells isolated between fractions from the homeostatic lung; bold font—differences in the proportion of protein-expressing cells between fractions postbleomycin treatment, and italics—overall differences in the proportion of protein-expressing cells between pre- and postbleomycin treatment regardless of fraction. No statistically significant differences were observed in the proportion of CD45-, <t>CD31-,</t> and EpCAM-positive cells between the density fractions in the homeostatic lung. In contrast, cells positive for c-KIT and CD49f were more prevalent in the lower fractions, while SCA-1 expressing cells equilibrated largely in the intermediate fractions. At day 2 following bleomycin treatment, only CD45-positive cells showed significant differences among the fractions equili- brating at the highest density (n ‡ 7; P = 0.01). (B) Representative western blots depicting levels of protein expression per fraction (n ‡ 4). The fibroblastic, smooth muscle, a1-actin (ACTA1) protein signal is highest in fractions 3 and 4 (P < 0.01 by densitometry). Levels of the epithelial (pro-) surfactant protein-C (SFTPC) and secretoglobin family 1A member 1 (SCGB1A1) protein bands are statistically significant between the fractions (P < 0.001 for both). Levels of the AT1 epithelial protein, aquaporin-5 (AQP5) are highest in the lighter fractions (P < 0.001). Bands representing levels of the endothelial CD31 protein and b-actin are also shown.
Labeled Streptavidin Biotin Staining Kit, supplied by Biogenex, 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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lsab+kit  (Agilent technologies)
90
Agilent technologies lsab+kit
FIG. 2. Density distribution of common lung cell lineages. (A) Fractionated cells from sham or 2-day bleomycin-treated mice were subjected to flow cytometry and average percent of cells ( – SEM) per fraction are presented. P-value represen- tations shown: normal font—differences in the proportion of protein-expressing cells isolated between fractions from the homeostatic lung; bold font—differences in the proportion of protein-expressing cells between fractions postbleomycin treatment, and italics—overall differences in the proportion of protein-expressing cells between pre- and postbleomycin treatment regardless of fraction. No statistically significant differences were observed in the proportion of CD45-, <t>CD31-,</t> and EpCAM-positive cells between the density fractions in the homeostatic lung. In contrast, cells positive for c-KIT and CD49f were more prevalent in the lower fractions, while SCA-1 expressing cells equilibrated largely in the intermediate fractions. At day 2 following bleomycin treatment, only CD45-positive cells showed significant differences among the fractions equili- brating at the highest density (n ‡ 7; P = 0.01). (B) Representative western blots depicting levels of protein expression per fraction (n ‡ 4). The fibroblastic, smooth muscle, a1-actin (ACTA1) protein signal is highest in fractions 3 and 4 (P < 0.01 by densitometry). Levels of the epithelial (pro-) surfactant protein-C (SFTPC) and secretoglobin family 1A member 1 (SCGB1A1) protein bands are statistically significant between the fractions (P < 0.001 for both). Levels of the AT1 epithelial protein, aquaporin-5 (AQP5) are highest in the lighter fractions (P < 0.001). Bands representing levels of the endothelial CD31 protein and b-actin are also shown.
Lsab+Kit, supplied by Agilent technologies, 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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biotin streptavidin reactions approach equilibrium  (Thermo Fisher)
99
Thermo Fisher biotin streptavidin reactions approach equilibrium
FIG. 2. Density distribution of common lung cell lineages. (A) Fractionated cells from sham or 2-day bleomycin-treated mice were subjected to flow cytometry and average percent of cells ( – SEM) per fraction are presented. P-value represen- tations shown: normal font—differences in the proportion of protein-expressing cells isolated between fractions from the homeostatic lung; bold font—differences in the proportion of protein-expressing cells between fractions postbleomycin treatment, and italics—overall differences in the proportion of protein-expressing cells between pre- and postbleomycin treatment regardless of fraction. No statistically significant differences were observed in the proportion of CD45-, <t>CD31-,</t> and EpCAM-positive cells between the density fractions in the homeostatic lung. In contrast, cells positive for c-KIT and CD49f were more prevalent in the lower fractions, while SCA-1 expressing cells equilibrated largely in the intermediate fractions. At day 2 following bleomycin treatment, only CD45-positive cells showed significant differences among the fractions equili- brating at the highest density (n ‡ 7; P = 0.01). (B) Representative western blots depicting levels of protein expression per fraction (n ‡ 4). The fibroblastic, smooth muscle, a1-actin (ACTA1) protein signal is highest in fractions 3 and 4 (P < 0.01 by densitometry). Levels of the epithelial (pro-) surfactant protein-C (SFTPC) and secretoglobin family 1A member 1 (SCGB1A1) protein bands are statistically significant between the fractions (P < 0.001 for both). Levels of the AT1 epithelial protein, aquaporin-5 (AQP5) are highest in the lighter fractions (P < 0.001). Bands representing levels of the endothelial CD31 protein and b-actin are also shown.
Biotin Streptavidin Reactions Approach Equilibrium, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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streptavidin biotin blocking kit  (Vector Laboratories)
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Vector Laboratories streptavidin biotin blocking kit
FIG. 2. Density distribution of common lung cell lineages. (A) Fractionated cells from sham or 2-day bleomycin-treated mice were subjected to flow cytometry and average percent of cells ( – SEM) per fraction are presented. P-value represen- tations shown: normal font—differences in the proportion of protein-expressing cells isolated between fractions from the homeostatic lung; bold font—differences in the proportion of protein-expressing cells between fractions postbleomycin treatment, and italics—overall differences in the proportion of protein-expressing cells between pre- and postbleomycin treatment regardless of fraction. No statistically significant differences were observed in the proportion of CD45-, <t>CD31-,</t> and EpCAM-positive cells between the density fractions in the homeostatic lung. In contrast, cells positive for c-KIT and CD49f were more prevalent in the lower fractions, while SCA-1 expressing cells equilibrated largely in the intermediate fractions. At day 2 following bleomycin treatment, only CD45-positive cells showed significant differences among the fractions equili- brating at the highest density (n ‡ 7; P = 0.01). (B) Representative western blots depicting levels of protein expression per fraction (n ‡ 4). The fibroblastic, smooth muscle, a1-actin (ACTA1) protein signal is highest in fractions 3 and 4 (P < 0.01 by densitometry). Levels of the epithelial (pro-) surfactant protein-C (SFTPC) and secretoglobin family 1A member 1 (SCGB1A1) protein bands are statistically significant between the fractions (P < 0.001 for both). Levels of the AT1 epithelial protein, aquaporin-5 (AQP5) are highest in the lighter fractions (P < 0.001). Bands representing levels of the endothelial CD31 protein and b-actin are also shown.
Streptavidin Biotin Blocking Kit, supplied by Vector Laboratories, 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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Image Search Results


FIG. 2. Density distribution of common lung cell lineages. (A) Fractionated cells from sham or 2-day bleomycin-treated mice were subjected to flow cytometry and average percent of cells ( – SEM) per fraction are presented. P-value represen- tations shown: normal font—differences in the proportion of protein-expressing cells isolated between fractions from the homeostatic lung; bold font—differences in the proportion of protein-expressing cells between fractions postbleomycin treatment, and italics—overall differences in the proportion of protein-expressing cells between pre- and postbleomycin treatment regardless of fraction. No statistically significant differences were observed in the proportion of CD45-, CD31-, and EpCAM-positive cells between the density fractions in the homeostatic lung. In contrast, cells positive for c-KIT and CD49f were more prevalent in the lower fractions, while SCA-1 expressing cells equilibrated largely in the intermediate fractions. At day 2 following bleomycin treatment, only CD45-positive cells showed significant differences among the fractions equili- brating at the highest density (n ‡ 7; P = 0.01). (B) Representative western blots depicting levels of protein expression per fraction (n ‡ 4). The fibroblastic, smooth muscle, a1-actin (ACTA1) protein signal is highest in fractions 3 and 4 (P < 0.01 by densitometry). Levels of the epithelial (pro-) surfactant protein-C (SFTPC) and secretoglobin family 1A member 1 (SCGB1A1) protein bands are statistically significant between the fractions (P < 0.001 for both). Levels of the AT1 epithelial protein, aquaporin-5 (AQP5) are highest in the lighter fractions (P < 0.001). Bands representing levels of the endothelial CD31 protein and b-actin are also shown.

Journal: Stem cells and development

Article Title: Discrimination between lung homeostatic and injury-induced epithelial progenitor subsets by cell-density properties.

doi: 10.1089/scd.2012.0468

Figure Lengend Snippet: FIG. 2. Density distribution of common lung cell lineages. (A) Fractionated cells from sham or 2-day bleomycin-treated mice were subjected to flow cytometry and average percent of cells ( – SEM) per fraction are presented. P-value represen- tations shown: normal font—differences in the proportion of protein-expressing cells isolated between fractions from the homeostatic lung; bold font—differences in the proportion of protein-expressing cells between fractions postbleomycin treatment, and italics—overall differences in the proportion of protein-expressing cells between pre- and postbleomycin treatment regardless of fraction. No statistically significant differences were observed in the proportion of CD45-, CD31-, and EpCAM-positive cells between the density fractions in the homeostatic lung. In contrast, cells positive for c-KIT and CD49f were more prevalent in the lower fractions, while SCA-1 expressing cells equilibrated largely in the intermediate fractions. At day 2 following bleomycin treatment, only CD45-positive cells showed significant differences among the fractions equili- brating at the highest density (n ‡ 7; P = 0.01). (B) Representative western blots depicting levels of protein expression per fraction (n ‡ 4). The fibroblastic, smooth muscle, a1-actin (ACTA1) protein signal is highest in fractions 3 and 4 (P < 0.01 by densitometry). Levels of the epithelial (pro-) surfactant protein-C (SFTPC) and secretoglobin family 1A member 1 (SCGB1A1) protein bands are statistically significant between the fractions (P < 0.001 for both). Levels of the AT1 epithelial protein, aquaporin-5 (AQP5) are highest in the lighter fractions (P < 0.001). Bands representing levels of the endothelial CD31 protein and b-actin are also shown.

Article Snippet: Flow cytometry and FACS analysis Fractionated cells were washed and labeled with the following antibodies: FITC-conjugated anti-CD45R (Invitrogen), R-PE anti- SCA-1 (Ly6A/E; Invitrogen), PE/Cy5 antic-KIT (CD117; eBioscience), PE-anti-CD49f (eBioscience), Alexa-488-anti-EpCAM (CD326; Biolegend, San Diego, CA), biotinylated-CD31 (Santa Cruz Biotech) followed by PE/Cy5 streptavidin (Biolegend), and mouse anti-BRDU (ebioscience) followed by anti-mouse Alexa 488 (Invitrogen).

Techniques: Cytometry, Expressing, Isolation, Western Blot

FIG. 3. Density properties of lung progenitor cell lineages. Sham or 2-day postbleomycin-treated mice were injected with BrdU, euthanized, and lungs harvested after 1 h. Cells were then dissociated, colabeled for BrdU and CD45, SCA-1, c-KIT, CD31, EpCAM, or CD49f, and processed for flow cytometry. (A) In untreated mice, BrdU-incorporating cells of FR3, primarily belonged to EpCAM and CD49f cell lineages. In contrast, BrdU-incorporating cells of fraction FR4 were SCA-1-positive (n ‡ 5). (B) Bleomycin treatment diminished the presence of BrdU-incorporating EpCAM and CD49f putative progenitor cells in fraction 3 introducing, instead, proliferating CD45, SCA-1, and c-KIT cell lineages to fraction 5 (n ‡ 4). Data are presented as average – SEM. (C) Re- presentative flow cytometry analysis of CD49f and EpCAM expression demonstrating the gating and percentage of sorted CD49f and EpCAMhi cells from density fractions.

Journal: Stem cells and development

Article Title: Discrimination between lung homeostatic and injury-induced epithelial progenitor subsets by cell-density properties.

doi: 10.1089/scd.2012.0468

Figure Lengend Snippet: FIG. 3. Density properties of lung progenitor cell lineages. Sham or 2-day postbleomycin-treated mice were injected with BrdU, euthanized, and lungs harvested after 1 h. Cells were then dissociated, colabeled for BrdU and CD45, SCA-1, c-KIT, CD31, EpCAM, or CD49f, and processed for flow cytometry. (A) In untreated mice, BrdU-incorporating cells of FR3, primarily belonged to EpCAM and CD49f cell lineages. In contrast, BrdU-incorporating cells of fraction FR4 were SCA-1-positive (n ‡ 5). (B) Bleomycin treatment diminished the presence of BrdU-incorporating EpCAM and CD49f putative progenitor cells in fraction 3 introducing, instead, proliferating CD45, SCA-1, and c-KIT cell lineages to fraction 5 (n ‡ 4). Data are presented as average – SEM. (C) Re- presentative flow cytometry analysis of CD49f and EpCAM expression demonstrating the gating and percentage of sorted CD49f and EpCAMhi cells from density fractions.

Article Snippet: Flow cytometry and FACS analysis Fractionated cells were washed and labeled with the following antibodies: FITC-conjugated anti-CD45R (Invitrogen), R-PE anti- SCA-1 (Ly6A/E; Invitrogen), PE/Cy5 antic-KIT (CD117; eBioscience), PE-anti-CD49f (eBioscience), Alexa-488-anti-EpCAM (CD326; Biolegend, San Diego, CA), biotinylated-CD31 (Santa Cruz Biotech) followed by PE/Cy5 streptavidin (Biolegend), and mouse anti-BRDU (ebioscience) followed by anti-mouse Alexa 488 (Invitrogen).

Techniques: Injection, Cytometry, Expressing