rabbit anti becn1 Search Results


rabbit igg anti-human becn1  (Assay Designs Inc)
90
Assay Designs Inc rabbit igg anti-human becn1
(A) Protein contents from tuberculoid (T-lep) and lepromatous (L-lep) lesion cells were analyzed by western blot with <t>anti-BECN1</t> and anti-BCL2 antibodies. GAPDH antibody was used to verify protein amount loading. Densitometric band-intensity analysis of the blots was realized and the BECN1/GAPDH (T-lep, n = 6; L-lep, n = 5) and BCL2/GAPDH (T-lep, n = 4; L-lep, n = 4) ratios were expressed as arbitrary units (AU). Bars represent the mean values ± SEM. * P < 0.05, Mann-Whitney test. (B) Macrophages (MΦs) were isolated from skin lesions of T-lep and L-lep patients and cultured for 7 days in full medium. Cells were fixed and labeled for BECN1 (red), BCL2 (green) and DAPI (blue). Cytoplasmatic BCL2 colocalizes with BECN1 in L-lep MΦs, but not in T-lep MΦs. Colocalization profiles between cytosolic BCL2 dots and BECN1 were quantified and expressed as percentage of cell area. The expression of nuclear compartment-associated BCL2 was excluded from the analysis. Results represent the mean ± SEM from one of three immunofluorescence experiments that yielded similar results. ** P < 0.01, Mann-Whitney test. Scale bar: 10 μm.
Rabbit Igg Anti Human Becn1, supplied by Assay Designs Inc, 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/rabbit igg anti-human becn1/product/Assay Designs Inc
Average 90 stars, based on 1 article reviews
rabbit igg anti-human becn1 - by Bioz Stars, 2026-02
90/100 stars
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primers for the κb site in the becn1 promoter  (Sangon Biotech)
90
Sangon Biotech primers for the κb site in the becn1 promoter
(A) Protein contents from tuberculoid (T-lep) and lepromatous (L-lep) lesion cells were analyzed by western blot with <t>anti-BECN1</t> and anti-BCL2 antibodies. GAPDH antibody was used to verify protein amount loading. Densitometric band-intensity analysis of the blots was realized and the BECN1/GAPDH (T-lep, n = 6; L-lep, n = 5) and BCL2/GAPDH (T-lep, n = 4; L-lep, n = 4) ratios were expressed as arbitrary units (AU). Bars represent the mean values ± SEM. * P < 0.05, Mann-Whitney test. (B) Macrophages (MΦs) were isolated from skin lesions of T-lep and L-lep patients and cultured for 7 days in full medium. Cells were fixed and labeled for BECN1 (red), BCL2 (green) and DAPI (blue). Cytoplasmatic BCL2 colocalizes with BECN1 in L-lep MΦs, but not in T-lep MΦs. Colocalization profiles between cytosolic BCL2 dots and BECN1 were quantified and expressed as percentage of cell area. The expression of nuclear compartment-associated BCL2 was excluded from the analysis. Results represent the mean ± SEM from one of three immunofluorescence experiments that yielded similar results. ** P < 0.01, Mann-Whitney test. Scale bar: 10 μm.
Primers For The κb Site In The Becn1 Promoter, supplied by Sangon Biotech, 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/primers for the κb site in the becn1 promoter/product/Sangon Biotech
Average 90 stars, based on 1 article reviews
primers for the κb site in the becn1 promoter - by Bioz Stars, 2026-02
90/100 stars
  Buy from Supplier
anti becn1  (Cusabio)
92
Cusabio anti becn1
(A) Protein contents from tuberculoid (T-lep) and lepromatous (L-lep) lesion cells were analyzed by western blot with <t>anti-BECN1</t> and anti-BCL2 antibodies. GAPDH antibody was used to verify protein amount loading. Densitometric band-intensity analysis of the blots was realized and the BECN1/GAPDH (T-lep, n = 6; L-lep, n = 5) and BCL2/GAPDH (T-lep, n = 4; L-lep, n = 4) ratios were expressed as arbitrary units (AU). Bars represent the mean values ± SEM. * P < 0.05, Mann-Whitney test. (B) Macrophages (MΦs) were isolated from skin lesions of T-lep and L-lep patients and cultured for 7 days in full medium. Cells were fixed and labeled for BECN1 (red), BCL2 (green) and DAPI (blue). Cytoplasmatic BCL2 colocalizes with BECN1 in L-lep MΦs, but not in T-lep MΦs. Colocalization profiles between cytosolic BCL2 dots and BECN1 were quantified and expressed as percentage of cell area. The expression of nuclear compartment-associated BCL2 was excluded from the analysis. Results represent the mean ± SEM from one of three immunofluorescence experiments that yielded similar results. ** P < 0.01, Mann-Whitney test. Scale bar: 10 μm.
Anti Becn1, 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
https://www.bioz.com/result/anti becn1/product/Cusabio
Average 92 stars, based on 1 article reviews
anti becn1 - by Bioz Stars, 2026-02
92/100 stars
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anti-beclin 1/becn1 antibody picoband  (Boster Bio)
93
Boster Bio anti-beclin 1/becn1 antibody picoband
(A) Protein contents from tuberculoid (T-lep) and lepromatous (L-lep) lesion cells were analyzed by western blot with <t>anti-BECN1</t> and anti-BCL2 antibodies. GAPDH antibody was used to verify protein amount loading. Densitometric band-intensity analysis of the blots was realized and the BECN1/GAPDH (T-lep, n = 6; L-lep, n = 5) and BCL2/GAPDH (T-lep, n = 4; L-lep, n = 4) ratios were expressed as arbitrary units (AU). Bars represent the mean values ± SEM. * P < 0.05, Mann-Whitney test. (B) Macrophages (MΦs) were isolated from skin lesions of T-lep and L-lep patients and cultured for 7 days in full medium. Cells were fixed and labeled for BECN1 (red), BCL2 (green) and DAPI (blue). Cytoplasmatic BCL2 colocalizes with BECN1 in L-lep MΦs, but not in T-lep MΦs. Colocalization profiles between cytosolic BCL2 dots and BECN1 were quantified and expressed as percentage of cell area. The expression of nuclear compartment-associated BCL2 was excluded from the analysis. Results represent the mean ± SEM from one of three immunofluorescence experiments that yielded similar results. ** P < 0.01, Mann-Whitney test. Scale bar: 10 μm.
Anti Beclin 1/Becn1 Antibody Picoband, supplied by Boster Bio, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/anti-beclin 1/becn1 antibody picoband/product/Boster Bio
Average 93 stars, based on 1 article reviews
anti-beclin 1/becn1 antibody picoband - by Bioz Stars, 2026-02
93/100 stars
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rabbit anti-becn1 (1:1000)  (ZenBio)
90
ZenBio rabbit anti-becn1 (1:1000)
(A) Protein contents from tuberculoid (T-lep) and lepromatous (L-lep) lesion cells were analyzed by western blot with <t>anti-BECN1</t> and anti-BCL2 antibodies. GAPDH antibody was used to verify protein amount loading. Densitometric band-intensity analysis of the blots was realized and the BECN1/GAPDH (T-lep, n = 6; L-lep, n = 5) and BCL2/GAPDH (T-lep, n = 4; L-lep, n = 4) ratios were expressed as arbitrary units (AU). Bars represent the mean values ± SEM. * P < 0.05, Mann-Whitney test. (B) Macrophages (MΦs) were isolated from skin lesions of T-lep and L-lep patients and cultured for 7 days in full medium. Cells were fixed and labeled for BECN1 (red), BCL2 (green) and DAPI (blue). Cytoplasmatic BCL2 colocalizes with BECN1 in L-lep MΦs, but not in T-lep MΦs. Colocalization profiles between cytosolic BCL2 dots and BECN1 were quantified and expressed as percentage of cell area. The expression of nuclear compartment-associated BCL2 was excluded from the analysis. Results represent the mean ± SEM from one of three immunofluorescence experiments that yielded similar results. ** P < 0.01, Mann-Whitney test. Scale bar: 10 μm.
Rabbit Anti Becn1 (1:1000), supplied by ZenBio, 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/rabbit anti-becn1 (1:1000)/product/ZenBio
Average 90 stars, based on 1 article reviews
rabbit anti-becn1 (1:1000) - by Bioz Stars, 2026-02
90/100 stars
  Buy from Supplier

Image Search Results


(A) Protein contents from tuberculoid (T-lep) and lepromatous (L-lep) lesion cells were analyzed by western blot with anti-BECN1 and anti-BCL2 antibodies. GAPDH antibody was used to verify protein amount loading. Densitometric band-intensity analysis of the blots was realized and the BECN1/GAPDH (T-lep, n = 6; L-lep, n = 5) and BCL2/GAPDH (T-lep, n = 4; L-lep, n = 4) ratios were expressed as arbitrary units (AU). Bars represent the mean values ± SEM. * P < 0.05, Mann-Whitney test. (B) Macrophages (MΦs) were isolated from skin lesions of T-lep and L-lep patients and cultured for 7 days in full medium. Cells were fixed and labeled for BECN1 (red), BCL2 (green) and DAPI (blue). Cytoplasmatic BCL2 colocalizes with BECN1 in L-lep MΦs, but not in T-lep MΦs. Colocalization profiles between cytosolic BCL2 dots and BECN1 were quantified and expressed as percentage of cell area. The expression of nuclear compartment-associated BCL2 was excluded from the analysis. Results represent the mean ± SEM from one of three immunofluorescence experiments that yielded similar results. ** P < 0.01, Mann-Whitney test. Scale bar: 10 μm.

Journal: PLoS Pathogens

Article Title: Autophagy Is an Innate Mechanism Associated with Leprosy Polarization

doi: 10.1371/journal.ppat.1006103

Figure Lengend Snippet: (A) Protein contents from tuberculoid (T-lep) and lepromatous (L-lep) lesion cells were analyzed by western blot with anti-BECN1 and anti-BCL2 antibodies. GAPDH antibody was used to verify protein amount loading. Densitometric band-intensity analysis of the blots was realized and the BECN1/GAPDH (T-lep, n = 6; L-lep, n = 5) and BCL2/GAPDH (T-lep, n = 4; L-lep, n = 4) ratios were expressed as arbitrary units (AU). Bars represent the mean values ± SEM. * P < 0.05, Mann-Whitney test. (B) Macrophages (MΦs) were isolated from skin lesions of T-lep and L-lep patients and cultured for 7 days in full medium. Cells were fixed and labeled for BECN1 (red), BCL2 (green) and DAPI (blue). Cytoplasmatic BCL2 colocalizes with BECN1 in L-lep MΦs, but not in T-lep MΦs. Colocalization profiles between cytosolic BCL2 dots and BECN1 were quantified and expressed as percentage of cell area. The expression of nuclear compartment-associated BCL2 was excluded from the analysis. Results represent the mean ± SEM from one of three immunofluorescence experiments that yielded similar results. ** P < 0.01, Mann-Whitney test. Scale bar: 10 μm.

Article Snippet: The buffer was then removed and the following primary antibodies were added: mouse IgG1 anti-human LC3 (1:50; MBL International), mouse IgG2b anti-human CD68/SR-D1 (1:100; R&D Systems, MAB20401), rabbit IgG anti-LAM (1:50; kindly donated by Dr. John Stewart Spencer from the Mycobacteria Research Laboratories, Colorado State University), rabbit IgG anti-human BECN1 (1:500; Assay Designs), and mouse IgG1 anti-human BCL2 (1:100; Dako), and incubated overnight at 4°C.

Techniques: Western Blot, MANN-WHITNEY, Isolation, Cell Culture, Labeling, Expressing, Immunofluorescence