ltl lotus tetraglobulus lectin vector laboratories cat fl 1321 Search Results


96
Vector Laboratories ltl
A , Schematic representation of the Six2VegfC mouse model where Six2 + nephron progenitor cells overexpress the growth factor VEGF-C which interacts with lymphatic endothelial cells (LECs) to promote lymphangiogenesis during kidney development. B , Representative images of Six2Vegf-C mice and littermate controls (Ctrl). Six2Vegf-C mice appear runted and have enlarged appearing kidneys of varying severity. Scale bar: 1 mm. C , Mouse weight in grams (g) and serum blood urea nitrogen (BUN) demonstrate reduced weight and kidney function in Six2Vegf-C mice. All data are presented as ±SE. Statistical comparisons were made using an unpaired t test. ***P = 0.0001 and ****P < 0.0001. D , Representative images of H&E stained kidney sections from Six2Vegf-C mice and littermate controls at postnatal day 1 (P1), P14, and 1 month of age demonstrating progressive peripelvic cystic lesions. Scale bar: 200 μm (P1), 500 μm (P14), 500 μm (1 month). E , Higher magnificent images of PAS stained kidney sections from Six2Vegf-C mice. Scale bar: 500 μm (4x), 25 μm (40x). F , Immunofluorescence of Six2Vegf-C kidney cystic lesions labeled for podoplanin (PDPN), LYVE1, VEGFR3, <t>endomucin</t> <t>(EMCN),</t> PDGFRB, Lotus tetraglobulus lectin <t>(LTL),</t> NA/K-ATPase, calbindin 1 (CALB1), pan-keratin (KER), cadherin-1 (CHD1). Scale bar: 50 μm. N ≥ 3 animals/group for all representative images.
Ltl, 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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95
Cell Signaling Technology Inc pan keratin
A , Schematic representation of the Six2VegfC mouse model where Six2 + nephron progenitor cells overexpress the growth factor VEGF-C which interacts with lymphatic endothelial cells (LECs) to promote lymphangiogenesis during kidney development. B , Representative images of Six2Vegf-C mice and littermate controls (Ctrl). Six2Vegf-C mice appear runted and have enlarged appearing kidneys of varying severity. Scale bar: 1 mm. C , Mouse weight in grams (g) and serum blood urea nitrogen (BUN) demonstrate reduced weight and kidney function in Six2Vegf-C mice. All data are presented as ±SE. Statistical comparisons were made using an unpaired t test. ***P = 0.0001 and ****P < 0.0001. D , Representative images of H&E stained kidney sections from Six2Vegf-C mice and littermate controls at postnatal day 1 (P1), P14, and 1 month of age demonstrating progressive peripelvic cystic lesions. Scale bar: 200 μm (P1), 500 μm (P14), 500 μm (1 month). E , Higher magnificent images of PAS stained kidney sections from Six2Vegf-C mice. Scale bar: 500 μm (4x), 25 μm (40x). F , Immunofluorescence of Six2Vegf-C kidney cystic lesions labeled for podoplanin (PDPN), LYVE1, VEGFR3, <t>endomucin</t> <t>(EMCN),</t> PDGFRB, Lotus tetraglobulus lectin <t>(LTL),</t> NA/K-ATPase, calbindin 1 (CALB1), pan-keratin (KER), cadherin-1 (CHD1). Scale bar: 50 μm. N ≥ 3 animals/group for all representative images.
Pan Keratin, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 95 stars, based on 1 article reviews
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95
Cell Signaling Technology Inc calb1
A , Schematic representation of the Six2VegfC mouse model where Six2 + nephron progenitor cells overexpress the growth factor VEGF-C which interacts with lymphatic endothelial cells (LECs) to promote lymphangiogenesis during kidney development. B , Representative images of Six2Vegf-C mice and littermate controls (Ctrl). Six2Vegf-C mice appear runted and have enlarged appearing kidneys of varying severity. Scale bar: 1 mm. C , Mouse weight in grams (g) and serum blood urea nitrogen (BUN) demonstrate reduced weight and kidney function in Six2Vegf-C mice. All data are presented as ±SE. Statistical comparisons were made using an unpaired t test. ***P = 0.0001 and ****P < 0.0001. D , Representative images of H&E stained kidney sections from Six2Vegf-C mice and littermate controls at postnatal day 1 (P1), P14, and 1 month of age demonstrating progressive peripelvic cystic lesions. Scale bar: 200 μm (P1), 500 μm (P14), 500 μm (1 month). E , Higher magnificent images of PAS stained kidney sections from Six2Vegf-C mice. Scale bar: 500 μm (4x), 25 μm (40x). F , Immunofluorescence of Six2Vegf-C kidney cystic lesions labeled for podoplanin (PDPN), LYVE1, VEGFR3, endomucin (EMCN), PDGFRB, Lotus tetraglobulus lectin (LTL), NA/K-ATPase, calbindin 1 <t>(CALB1),</t> pan-keratin (KER), cadherin-1 (CHD1). Scale bar: 50 μm. N ≥ 3 animals/group for all representative images.
Calb1, supplied by Cell Signaling Technology Inc, 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/product/ltl+lotus+tetraglobulus+lectin+vector+laboratories+cat+fl+1321/Calbindin+XP+Rabbit+mAb/bio_rxiv__2023__05__03__538868-86-61-62
Average 95 stars, based on 1 article reviews
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98
Cell Signaling Technology Inc cdh1
A , Schematic representation of the Six2VegfC mouse model where Six2 + nephron progenitor cells overexpress the growth factor VEGF-C which interacts with lymphatic endothelial cells (LECs) to promote lymphangiogenesis during kidney development. B , Representative images of Six2Vegf-C mice and littermate controls (Ctrl). Six2Vegf-C mice appear runted and have enlarged appearing kidneys of varying severity. Scale bar: 1 mm. C , Mouse weight in grams (g) and serum blood urea nitrogen (BUN) demonstrate reduced weight and kidney function in Six2Vegf-C mice. All data are presented as ±SE. Statistical comparisons were made using an unpaired t test. ***P = 0.0001 and ****P < 0.0001. D , Representative images of H&E stained kidney sections from Six2Vegf-C mice and littermate controls at postnatal day 1 (P1), P14, and 1 month of age demonstrating progressive peripelvic cystic lesions. Scale bar: 200 μm (P1), 500 μm (P14), 500 μm (1 month). E , Higher magnificent images of PAS stained kidney sections from Six2Vegf-C mice. Scale bar: 500 μm (4x), 25 μm (40x). F , Immunofluorescence of Six2Vegf-C kidney cystic lesions labeled for podoplanin (PDPN), LYVE1, VEGFR3, endomucin (EMCN), PDGFRB, Lotus tetraglobulus lectin (LTL), NA/K-ATPase, calbindin 1 (CALB1), pan-keratin (KER), <t>cadherin-1</t> (CHD1). Scale bar: 50 μm. N ≥ 3 animals/group for all representative images.
Cdh1, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ltl+lotus+tetraglobulus+lectin+vector+laboratories+cat+fl+1321/E-Cadherin+Rabbit+mAb/bio_rxiv__2023__05__03__538868-86-70-71
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Image Search Results


A , Schematic representation of the Six2VegfC mouse model where Six2 + nephron progenitor cells overexpress the growth factor VEGF-C which interacts with lymphatic endothelial cells (LECs) to promote lymphangiogenesis during kidney development. B , Representative images of Six2Vegf-C mice and littermate controls (Ctrl). Six2Vegf-C mice appear runted and have enlarged appearing kidneys of varying severity. Scale bar: 1 mm. C , Mouse weight in grams (g) and serum blood urea nitrogen (BUN) demonstrate reduced weight and kidney function in Six2Vegf-C mice. All data are presented as ±SE. Statistical comparisons were made using an unpaired t test. ***P = 0.0001 and ****P < 0.0001. D , Representative images of H&E stained kidney sections from Six2Vegf-C mice and littermate controls at postnatal day 1 (P1), P14, and 1 month of age demonstrating progressive peripelvic cystic lesions. Scale bar: 200 μm (P1), 500 μm (P14), 500 μm (1 month). E , Higher magnificent images of PAS stained kidney sections from Six2Vegf-C mice. Scale bar: 500 μm (4x), 25 μm (40x). F , Immunofluorescence of Six2Vegf-C kidney cystic lesions labeled for podoplanin (PDPN), LYVE1, VEGFR3, endomucin (EMCN), PDGFRB, Lotus tetraglobulus lectin (LTL), NA/K-ATPase, calbindin 1 (CALB1), pan-keratin (KER), cadherin-1 (CHD1). Scale bar: 50 μm. N ≥ 3 animals/group for all representative images.

Journal: bioRxiv

Article Title: VEGF-C overexpression in kidney progenitor cells is a model of renal lymphangiectasia

doi: 10.1101/2023.05.03.538868

Figure Lengend Snippet: A , Schematic representation of the Six2VegfC mouse model where Six2 + nephron progenitor cells overexpress the growth factor VEGF-C which interacts with lymphatic endothelial cells (LECs) to promote lymphangiogenesis during kidney development. B , Representative images of Six2Vegf-C mice and littermate controls (Ctrl). Six2Vegf-C mice appear runted and have enlarged appearing kidneys of varying severity. Scale bar: 1 mm. C , Mouse weight in grams (g) and serum blood urea nitrogen (BUN) demonstrate reduced weight and kidney function in Six2Vegf-C mice. All data are presented as ±SE. Statistical comparisons were made using an unpaired t test. ***P = 0.0001 and ****P < 0.0001. D , Representative images of H&E stained kidney sections from Six2Vegf-C mice and littermate controls at postnatal day 1 (P1), P14, and 1 month of age demonstrating progressive peripelvic cystic lesions. Scale bar: 200 μm (P1), 500 μm (P14), 500 μm (1 month). E , Higher magnificent images of PAS stained kidney sections from Six2Vegf-C mice. Scale bar: 500 μm (4x), 25 μm (40x). F , Immunofluorescence of Six2Vegf-C kidney cystic lesions labeled for podoplanin (PDPN), LYVE1, VEGFR3, endomucin (EMCN), PDGFRB, Lotus tetraglobulus lectin (LTL), NA/K-ATPase, calbindin 1 (CALB1), pan-keratin (KER), cadherin-1 (CHD1). Scale bar: 50 μm. N ≥ 3 animals/group for all representative images.

Article Snippet: Standard methods for immunofluorescence processing were carried out following heat induced antigen retrieval by citrate buffer (0.01M; pH 6.0) using the following antibodies: PDPN (DSHB Cat# 8.1.1), LYVE1 (R&D Cat# AF2125), VEGFR3 (R&D Cat# AF743), NRP2 (R&D Cat# AF567 EMCN (Abcam Cat# ab106100), PDGFRB (R&D Cat# AF1042), LTL ( Lotus tetraglobulus lectin ) (Vector Laboratories Cat# FL-1321), NA/K-ATPase (DSHB Cat# a5), CALB1 (CST Cat# 13176S), pan-Keratin (CST Cat# 4545S), and CDH1 (CST Cat# 3195S).

Techniques: Staining, Immunofluorescence, Labeling

A , Schematic representation of the Six2VegfC mouse model where Six2 + nephron progenitor cells overexpress the growth factor VEGF-C which interacts with lymphatic endothelial cells (LECs) to promote lymphangiogenesis during kidney development. B , Representative images of Six2Vegf-C mice and littermate controls (Ctrl). Six2Vegf-C mice appear runted and have enlarged appearing kidneys of varying severity. Scale bar: 1 mm. C , Mouse weight in grams (g) and serum blood urea nitrogen (BUN) demonstrate reduced weight and kidney function in Six2Vegf-C mice. All data are presented as ±SE. Statistical comparisons were made using an unpaired t test. ***P = 0.0001 and ****P < 0.0001. D , Representative images of H&E stained kidney sections from Six2Vegf-C mice and littermate controls at postnatal day 1 (P1), P14, and 1 month of age demonstrating progressive peripelvic cystic lesions. Scale bar: 200 μm (P1), 500 μm (P14), 500 μm (1 month). E , Higher magnificent images of PAS stained kidney sections from Six2Vegf-C mice. Scale bar: 500 μm (4x), 25 μm (40x). F , Immunofluorescence of Six2Vegf-C kidney cystic lesions labeled for podoplanin (PDPN), LYVE1, VEGFR3, endomucin (EMCN), PDGFRB, Lotus tetraglobulus lectin (LTL), NA/K-ATPase, calbindin 1 (CALB1), pan-keratin (KER), cadherin-1 (CHD1). Scale bar: 50 μm. N ≥ 3 animals/group for all representative images.

Journal: bioRxiv

Article Title: VEGF-C overexpression in kidney progenitor cells is a model of renal lymphangiectasia

doi: 10.1101/2023.05.03.538868

Figure Lengend Snippet: A , Schematic representation of the Six2VegfC mouse model where Six2 + nephron progenitor cells overexpress the growth factor VEGF-C which interacts with lymphatic endothelial cells (LECs) to promote lymphangiogenesis during kidney development. B , Representative images of Six2Vegf-C mice and littermate controls (Ctrl). Six2Vegf-C mice appear runted and have enlarged appearing kidneys of varying severity. Scale bar: 1 mm. C , Mouse weight in grams (g) and serum blood urea nitrogen (BUN) demonstrate reduced weight and kidney function in Six2Vegf-C mice. All data are presented as ±SE. Statistical comparisons were made using an unpaired t test. ***P = 0.0001 and ****P < 0.0001. D , Representative images of H&E stained kidney sections from Six2Vegf-C mice and littermate controls at postnatal day 1 (P1), P14, and 1 month of age demonstrating progressive peripelvic cystic lesions. Scale bar: 200 μm (P1), 500 μm (P14), 500 μm (1 month). E , Higher magnificent images of PAS stained kidney sections from Six2Vegf-C mice. Scale bar: 500 μm (4x), 25 μm (40x). F , Immunofluorescence of Six2Vegf-C kidney cystic lesions labeled for podoplanin (PDPN), LYVE1, VEGFR3, endomucin (EMCN), PDGFRB, Lotus tetraglobulus lectin (LTL), NA/K-ATPase, calbindin 1 (CALB1), pan-keratin (KER), cadherin-1 (CHD1). Scale bar: 50 μm. N ≥ 3 animals/group for all representative images.

Article Snippet: Standard methods for immunofluorescence processing were carried out following heat induced antigen retrieval by citrate buffer (0.01M; pH 6.0) using the following antibodies: PDPN (DSHB Cat# 8.1.1), LYVE1 (R&D Cat# AF2125), VEGFR3 (R&D Cat# AF743), NRP2 (R&D Cat# AF567 EMCN (Abcam Cat# ab106100), PDGFRB (R&D Cat# AF1042), LTL ( Lotus tetraglobulus lectin ) (Vector Laboratories Cat# FL-1321), NA/K-ATPase (DSHB Cat# a5), CALB1 (CST Cat# 13176S), pan-Keratin (CST Cat# 4545S), and CDH1 (CST Cat# 3195S).

Techniques: Staining, Immunofluorescence, Labeling

A , Schematic representation of the Six2VegfC mouse model where Six2 + nephron progenitor cells overexpress the growth factor VEGF-C which interacts with lymphatic endothelial cells (LECs) to promote lymphangiogenesis during kidney development. B , Representative images of Six2Vegf-C mice and littermate controls (Ctrl). Six2Vegf-C mice appear runted and have enlarged appearing kidneys of varying severity. Scale bar: 1 mm. C , Mouse weight in grams (g) and serum blood urea nitrogen (BUN) demonstrate reduced weight and kidney function in Six2Vegf-C mice. All data are presented as ±SE. Statistical comparisons were made using an unpaired t test. ***P = 0.0001 and ****P < 0.0001. D , Representative images of H&E stained kidney sections from Six2Vegf-C mice and littermate controls at postnatal day 1 (P1), P14, and 1 month of age demonstrating progressive peripelvic cystic lesions. Scale bar: 200 μm (P1), 500 μm (P14), 500 μm (1 month). E , Higher magnificent images of PAS stained kidney sections from Six2Vegf-C mice. Scale bar: 500 μm (4x), 25 μm (40x). F , Immunofluorescence of Six2Vegf-C kidney cystic lesions labeled for podoplanin (PDPN), LYVE1, VEGFR3, endomucin (EMCN), PDGFRB, Lotus tetraglobulus lectin (LTL), NA/K-ATPase, calbindin 1 (CALB1), pan-keratin (KER), cadherin-1 (CHD1). Scale bar: 50 μm. N ≥ 3 animals/group for all representative images.

Journal: bioRxiv

Article Title: VEGF-C overexpression in kidney progenitor cells is a model of renal lymphangiectasia

doi: 10.1101/2023.05.03.538868

Figure Lengend Snippet: A , Schematic representation of the Six2VegfC mouse model where Six2 + nephron progenitor cells overexpress the growth factor VEGF-C which interacts with lymphatic endothelial cells (LECs) to promote lymphangiogenesis during kidney development. B , Representative images of Six2Vegf-C mice and littermate controls (Ctrl). Six2Vegf-C mice appear runted and have enlarged appearing kidneys of varying severity. Scale bar: 1 mm. C , Mouse weight in grams (g) and serum blood urea nitrogen (BUN) demonstrate reduced weight and kidney function in Six2Vegf-C mice. All data are presented as ±SE. Statistical comparisons were made using an unpaired t test. ***P = 0.0001 and ****P < 0.0001. D , Representative images of H&E stained kidney sections from Six2Vegf-C mice and littermate controls at postnatal day 1 (P1), P14, and 1 month of age demonstrating progressive peripelvic cystic lesions. Scale bar: 200 μm (P1), 500 μm (P14), 500 μm (1 month). E , Higher magnificent images of PAS stained kidney sections from Six2Vegf-C mice. Scale bar: 500 μm (4x), 25 μm (40x). F , Immunofluorescence of Six2Vegf-C kidney cystic lesions labeled for podoplanin (PDPN), LYVE1, VEGFR3, endomucin (EMCN), PDGFRB, Lotus tetraglobulus lectin (LTL), NA/K-ATPase, calbindin 1 (CALB1), pan-keratin (KER), cadherin-1 (CHD1). Scale bar: 50 μm. N ≥ 3 animals/group for all representative images.

Article Snippet: Standard methods for immunofluorescence processing were carried out following heat induced antigen retrieval by citrate buffer (0.01M; pH 6.0) using the following antibodies: PDPN (DSHB Cat# 8.1.1), LYVE1 (R&D Cat# AF2125), VEGFR3 (R&D Cat# AF743), NRP2 (R&D Cat# AF567 EMCN (Abcam Cat# ab106100), PDGFRB (R&D Cat# AF1042), LTL ( Lotus tetraglobulus lectin ) (Vector Laboratories Cat# FL-1321), NA/K-ATPase (DSHB Cat# a5), CALB1 (CST Cat# 13176S), pan-Keratin (CST Cat# 4545S), and CDH1 (CST Cat# 3195S).

Techniques: Staining, Immunofluorescence, Labeling