h4a3 s mouse lamp1 antibody Search Results


99
Developmental Studies Hybridoma Bank h4a3 to lamp1
H4a3 To Lamp1, supplied by Developmental Studies Hybridoma Bank, 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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NSJ Bioreagents rab11b antibody
Rab11b Antibody, supplied by NSJ Bioreagents, 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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Santa Cruz Biotechnology mousemonoclonal anti lamp1 h4a3 s
Mousemonoclonal Anti Lamp1 H4a3 S, supplied by Santa Cruz Biotechnology, 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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91
Bioss cathepsin d ctsd polyclonal antibody
Cathepsin D Ctsd Polyclonal Antibody, supplied by Bioss, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Millipore anti-alix
PM damage is followed by recruitment of ALG-2 and ESCRT-III leading to PM repair and shedding of the damaged membrane (A) Micrograph of invasion pockets containing <t>C.</t> <t>albicans</t> . TR146 cells were transfected with CHMP2a-GFP (left), CHMP4B-mCherry (right). Side panels show the XY and YZ slices corresponding to areas marked by the dotted boxes. (B) Micrograph of pockets containing wild-type or ece1 Δ/Δ C. albicans . TR146 cells were transfected with CHMP2a-GFP (left), CHMP4B-mCherry (right), and PM bleb formation was assessed staining non-permeabilized cells with 10 μM FM4-64. Side panels show the XZ and YZ slices corresponding to the areas marked by the dotted boxes. (C) Micrographs of TR146 cells treated with 30 μM Ece1-VIIa peptide or candidalysin. Cells were transfected with CHMP2a-GFP and PM bleb formation assessed by staining non-permeabilized cells with 10 μM FM4-64. (A–C) Outlines of TR146 cells indicated by dotted lines. Scale bars represent 5 μm. (D) Confocal micrographs of TR146 cells infected with wild-type (left panel) or ece1 Δ/Δ mutant C. albicans (right panel). ALG-2 was detected by immunofluorescence. Scale bar represents 10 μm. (E) Quantification of ALG-2 accumulation as a function of invasion pocket length, from experiments like those in (D). Data are means ± SEM of ≥3 individual experiments. (F and G) Micrographs of TR146 cells treated with 30 μM candidalysin. ALG-2 (F) and <t>ALIX</t> (G) detected by immunofluorescence and PM blebs detected staining the PM with ConA. Images are representative of ≥3 experiments of each type. See also <xref ref-type=Figure S2 . " width="250" height="auto" />
Anti Alix, supplied by Millipore, 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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90
Developmental Studies Hybridoma Bank antibody #h4a3-s monoclonal anti-lamp1
PM damage is followed by recruitment of ALG-2 and ESCRT-III leading to PM repair and shedding of the damaged membrane (A) Micrograph of invasion pockets containing <t>C.</t> <t>albicans</t> . TR146 cells were transfected with CHMP2a-GFP (left), CHMP4B-mCherry (right). Side panels show the XY and YZ slices corresponding to areas marked by the dotted boxes. (B) Micrograph of pockets containing wild-type or ece1 Δ/Δ C. albicans . TR146 cells were transfected with CHMP2a-GFP (left), CHMP4B-mCherry (right), and PM bleb formation was assessed staining non-permeabilized cells with 10 μM FM4-64. Side panels show the XZ and YZ slices corresponding to the areas marked by the dotted boxes. (C) Micrographs of TR146 cells treated with 30 μM Ece1-VIIa peptide or candidalysin. Cells were transfected with CHMP2a-GFP and PM bleb formation assessed by staining non-permeabilized cells with 10 μM FM4-64. (A–C) Outlines of TR146 cells indicated by dotted lines. Scale bars represent 5 μm. (D) Confocal micrographs of TR146 cells infected with wild-type (left panel) or ece1 Δ/Δ mutant C. albicans (right panel). ALG-2 was detected by immunofluorescence. Scale bar represents 10 μm. (E) Quantification of ALG-2 accumulation as a function of invasion pocket length, from experiments like those in (D). Data are means ± SEM of ≥3 individual experiments. (F and G) Micrographs of TR146 cells treated with 30 μM candidalysin. ALG-2 (F) and <t>ALIX</t> (G) detected by immunofluorescence and PM blebs detected staining the PM with ConA. Images are representative of ≥3 experiments of each type. See also <xref ref-type=Figure S2 . " width="250" height="auto" />
Antibody #H4a3 S Monoclonal Anti Lamp1, supplied by Developmental Studies Hybridoma Bank, 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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96
Bioss 8-ohdg polyclonal antibody
PM damage is followed by recruitment of ALG-2 and ESCRT-III leading to PM repair and shedding of the damaged membrane (A) Micrograph of invasion pockets containing <t>C.</t> <t>albicans</t> . TR146 cells were transfected with CHMP2a-GFP (left), CHMP4B-mCherry (right). Side panels show the XY and YZ slices corresponding to areas marked by the dotted boxes. (B) Micrograph of pockets containing wild-type or ece1 Δ/Δ C. albicans . TR146 cells were transfected with CHMP2a-GFP (left), CHMP4B-mCherry (right), and PM bleb formation was assessed staining non-permeabilized cells with 10 μM FM4-64. Side panels show the XZ and YZ slices corresponding to the areas marked by the dotted boxes. (C) Micrographs of TR146 cells treated with 30 μM Ece1-VIIa peptide or candidalysin. Cells were transfected with CHMP2a-GFP and PM bleb formation assessed by staining non-permeabilized cells with 10 μM FM4-64. (A–C) Outlines of TR146 cells indicated by dotted lines. Scale bars represent 5 μm. (D) Confocal micrographs of TR146 cells infected with wild-type (left panel) or ece1 Δ/Δ mutant C. albicans (right panel). ALG-2 was detected by immunofluorescence. Scale bar represents 10 μm. (E) Quantification of ALG-2 accumulation as a function of invasion pocket length, from experiments like those in (D). Data are means ± SEM of ≥3 individual experiments. (F and G) Micrographs of TR146 cells treated with 30 μM candidalysin. ALG-2 (F) and <t>ALIX</t> (G) detected by immunofluorescence and PM blebs detected staining the PM with ConA. Images are representative of ≥3 experiments of each type. See also <xref ref-type=Figure S2 . " width="250" height="auto" />
8 Ohdg Polyclonal Antibody, supplied by Bioss, 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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92
Bioss prrsv m protein polyclonal antibody
PM damage is followed by recruitment of ALG-2 and ESCRT-III leading to PM repair and shedding of the damaged membrane (A) Micrograph of invasion pockets containing <t>C.</t> <t>albicans</t> . TR146 cells were transfected with CHMP2a-GFP (left), CHMP4B-mCherry (right). Side panels show the XY and YZ slices corresponding to areas marked by the dotted boxes. (B) Micrograph of pockets containing wild-type or ece1 Δ/Δ C. albicans . TR146 cells were transfected with CHMP2a-GFP (left), CHMP4B-mCherry (right), and PM bleb formation was assessed staining non-permeabilized cells with 10 μM FM4-64. Side panels show the XZ and YZ slices corresponding to the areas marked by the dotted boxes. (C) Micrographs of TR146 cells treated with 30 μM Ece1-VIIa peptide or candidalysin. Cells were transfected with CHMP2a-GFP and PM bleb formation assessed by staining non-permeabilized cells with 10 μM FM4-64. (A–C) Outlines of TR146 cells indicated by dotted lines. Scale bars represent 5 μm. (D) Confocal micrographs of TR146 cells infected with wild-type (left panel) or ece1 Δ/Δ mutant C. albicans (right panel). ALG-2 was detected by immunofluorescence. Scale bar represents 10 μm. (E) Quantification of ALG-2 accumulation as a function of invasion pocket length, from experiments like those in (D). Data are means ± SEM of ≥3 individual experiments. (F and G) Micrographs of TR146 cells treated with 30 μM candidalysin. ALG-2 (F) and <t>ALIX</t> (G) detected by immunofluorescence and PM blebs detected staining the PM with ConA. Images are representative of ≥3 experiments of each type. See also <xref ref-type=Figure S2 . " width="250" height="auto" />
Prrsv M Protein Polyclonal Antibody, supplied by Bioss, 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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prrsv m protein polyclonal antibody - by Bioz Stars, 2026-02
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92
Bioss collagen 7 polyclonal antibody
PM damage is followed by recruitment of ALG-2 and ESCRT-III leading to PM repair and shedding of the damaged membrane (A) Micrograph of invasion pockets containing <t>C.</t> <t>albicans</t> . TR146 cells were transfected with CHMP2a-GFP (left), CHMP4B-mCherry (right). Side panels show the XY and YZ slices corresponding to areas marked by the dotted boxes. (B) Micrograph of pockets containing wild-type or ece1 Δ/Δ C. albicans . TR146 cells were transfected with CHMP2a-GFP (left), CHMP4B-mCherry (right), and PM bleb formation was assessed staining non-permeabilized cells with 10 μM FM4-64. Side panels show the XZ and YZ slices corresponding to the areas marked by the dotted boxes. (C) Micrographs of TR146 cells treated with 30 μM Ece1-VIIa peptide or candidalysin. Cells were transfected with CHMP2a-GFP and PM bleb formation assessed by staining non-permeabilized cells with 10 μM FM4-64. (A–C) Outlines of TR146 cells indicated by dotted lines. Scale bars represent 5 μm. (D) Confocal micrographs of TR146 cells infected with wild-type (left panel) or ece1 Δ/Δ mutant C. albicans (right panel). ALG-2 was detected by immunofluorescence. Scale bar represents 10 μm. (E) Quantification of ALG-2 accumulation as a function of invasion pocket length, from experiments like those in (D). Data are means ± SEM of ≥3 individual experiments. (F and G) Micrographs of TR146 cells treated with 30 μM candidalysin. ALG-2 (F) and <t>ALIX</t> (G) detected by immunofluorescence and PM blebs detected staining the PM with ConA. Images are representative of ≥3 experiments of each type. See also <xref ref-type=Figure S2 . " width="250" height="auto" />
Collagen 7 Polyclonal Antibody, supplied by Bioss, 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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94
Bioss cd16 polyclonal antibody
PM damage is followed by recruitment of ALG-2 and ESCRT-III leading to PM repair and shedding of the damaged membrane (A) Micrograph of invasion pockets containing <t>C.</t> <t>albicans</t> . TR146 cells were transfected with CHMP2a-GFP (left), CHMP4B-mCherry (right). Side panels show the XY and YZ slices corresponding to areas marked by the dotted boxes. (B) Micrograph of pockets containing wild-type or ece1 Δ/Δ C. albicans . TR146 cells were transfected with CHMP2a-GFP (left), CHMP4B-mCherry (right), and PM bleb formation was assessed staining non-permeabilized cells with 10 μM FM4-64. Side panels show the XZ and YZ slices corresponding to the areas marked by the dotted boxes. (C) Micrographs of TR146 cells treated with 30 μM Ece1-VIIa peptide or candidalysin. Cells were transfected with CHMP2a-GFP and PM bleb formation assessed by staining non-permeabilized cells with 10 μM FM4-64. (A–C) Outlines of TR146 cells indicated by dotted lines. Scale bars represent 5 μm. (D) Confocal micrographs of TR146 cells infected with wild-type (left panel) or ece1 Δ/Δ mutant C. albicans (right panel). ALG-2 was detected by immunofluorescence. Scale bar represents 10 μm. (E) Quantification of ALG-2 accumulation as a function of invasion pocket length, from experiments like those in (D). Data are means ± SEM of ≥3 individual experiments. (F and G) Micrographs of TR146 cells treated with 30 μM candidalysin. ALG-2 (F) and <t>ALIX</t> (G) detected by immunofluorescence and PM blebs detected staining the PM with ConA. Images are representative of ≥3 experiments of each type. See also <xref ref-type=Figure S2 . " width="250" height="auto" />
Cd16 Polyclonal Antibody, supplied by Bioss, 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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Bioss vimentin polyclonal antibody
PM damage is followed by recruitment of ALG-2 and ESCRT-III leading to PM repair and shedding of the damaged membrane (A) Micrograph of invasion pockets containing <t>C.</t> <t>albicans</t> . TR146 cells were transfected with CHMP2a-GFP (left), CHMP4B-mCherry (right). Side panels show the XY and YZ slices corresponding to areas marked by the dotted boxes. (B) Micrograph of pockets containing wild-type or ece1 Δ/Δ C. albicans . TR146 cells were transfected with CHMP2a-GFP (left), CHMP4B-mCherry (right), and PM bleb formation was assessed staining non-permeabilized cells with 10 μM FM4-64. Side panels show the XZ and YZ slices corresponding to the areas marked by the dotted boxes. (C) Micrographs of TR146 cells treated with 30 μM Ece1-VIIa peptide or candidalysin. Cells were transfected with CHMP2a-GFP and PM bleb formation assessed by staining non-permeabilized cells with 10 μM FM4-64. (A–C) Outlines of TR146 cells indicated by dotted lines. Scale bars represent 5 μm. (D) Confocal micrographs of TR146 cells infected with wild-type (left panel) or ece1 Δ/Δ mutant C. albicans (right panel). ALG-2 was detected by immunofluorescence. Scale bar represents 10 μm. (E) Quantification of ALG-2 accumulation as a function of invasion pocket length, from experiments like those in (D). Data are means ± SEM of ≥3 individual experiments. (F and G) Micrographs of TR146 cells treated with 30 μM candidalysin. ALG-2 (F) and <t>ALIX</t> (G) detected by immunofluorescence and PM blebs detected staining the PM with ConA. Images are representative of ≥3 experiments of each type. See also <xref ref-type=Figure S2 . " width="250" height="auto" />
Vimentin Polyclonal Antibody, supplied by Bioss, 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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Bioss cdc2/cdk1 polyclonal antibody
PM damage is followed by recruitment of ALG-2 and ESCRT-III leading to PM repair and shedding of the damaged membrane (A) Micrograph of invasion pockets containing <t>C.</t> <t>albicans</t> . TR146 cells were transfected with CHMP2a-GFP (left), CHMP4B-mCherry (right). Side panels show the XY and YZ slices corresponding to areas marked by the dotted boxes. (B) Micrograph of pockets containing wild-type or ece1 Δ/Δ C. albicans . TR146 cells were transfected with CHMP2a-GFP (left), CHMP4B-mCherry (right), and PM bleb formation was assessed staining non-permeabilized cells with 10 μM FM4-64. Side panels show the XZ and YZ slices corresponding to the areas marked by the dotted boxes. (C) Micrographs of TR146 cells treated with 30 μM Ece1-VIIa peptide or candidalysin. Cells were transfected with CHMP2a-GFP and PM bleb formation assessed by staining non-permeabilized cells with 10 μM FM4-64. (A–C) Outlines of TR146 cells indicated by dotted lines. Scale bars represent 5 μm. (D) Confocal micrographs of TR146 cells infected with wild-type (left panel) or ece1 Δ/Δ mutant C. albicans (right panel). ALG-2 was detected by immunofluorescence. Scale bar represents 10 μm. (E) Quantification of ALG-2 accumulation as a function of invasion pocket length, from experiments like those in (D). Data are means ± SEM of ≥3 individual experiments. (F and G) Micrographs of TR146 cells treated with 30 μM candidalysin. ALG-2 (F) and <t>ALIX</t> (G) detected by immunofluorescence and PM blebs detected staining the PM with ConA. Images are representative of ≥3 experiments of each type. See also <xref ref-type=Figure S2 . " width="250" height="auto" />
Cdc2/Cdk1 Polyclonal Antibody, supplied by Bioss, 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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cdc2/cdk1 polyclonal antibody - by Bioz Stars, 2026-02
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Image Search Results


PM damage is followed by recruitment of ALG-2 and ESCRT-III leading to PM repair and shedding of the damaged membrane (A) Micrograph of invasion pockets containing C. albicans . TR146 cells were transfected with CHMP2a-GFP (left), CHMP4B-mCherry (right). Side panels show the XY and YZ slices corresponding to areas marked by the dotted boxes. (B) Micrograph of pockets containing wild-type or ece1 Δ/Δ C. albicans . TR146 cells were transfected with CHMP2a-GFP (left), CHMP4B-mCherry (right), and PM bleb formation was assessed staining non-permeabilized cells with 10 μM FM4-64. Side panels show the XZ and YZ slices corresponding to the areas marked by the dotted boxes. (C) Micrographs of TR146 cells treated with 30 μM Ece1-VIIa peptide or candidalysin. Cells were transfected with CHMP2a-GFP and PM bleb formation assessed by staining non-permeabilized cells with 10 μM FM4-64. (A–C) Outlines of TR146 cells indicated by dotted lines. Scale bars represent 5 μm. (D) Confocal micrographs of TR146 cells infected with wild-type (left panel) or ece1 Δ/Δ mutant C. albicans (right panel). ALG-2 was detected by immunofluorescence. Scale bar represents 10 μm. (E) Quantification of ALG-2 accumulation as a function of invasion pocket length, from experiments like those in (D). Data are means ± SEM of ≥3 individual experiments. (F and G) Micrographs of TR146 cells treated with 30 μM candidalysin. ALG-2 (F) and ALIX (G) detected by immunofluorescence and PM blebs detected staining the PM with ConA. Images are representative of ≥3 experiments of each type. See also <xref ref-type=Figure S2 . " width="100%" height="100%">

Journal: Cell Reports

Article Title: Calcium-dependent ESCRT recruitment and lysosome exocytosis maintain epithelial integrity during Candida albicans invasion

doi: 10.1016/j.celrep.2021.110187

Figure Lengend Snippet: PM damage is followed by recruitment of ALG-2 and ESCRT-III leading to PM repair and shedding of the damaged membrane (A) Micrograph of invasion pockets containing C. albicans . TR146 cells were transfected with CHMP2a-GFP (left), CHMP4B-mCherry (right). Side panels show the XY and YZ slices corresponding to areas marked by the dotted boxes. (B) Micrograph of pockets containing wild-type or ece1 Δ/Δ C. albicans . TR146 cells were transfected with CHMP2a-GFP (left), CHMP4B-mCherry (right), and PM bleb formation was assessed staining non-permeabilized cells with 10 μM FM4-64. Side panels show the XZ and YZ slices corresponding to the areas marked by the dotted boxes. (C) Micrographs of TR146 cells treated with 30 μM Ece1-VIIa peptide or candidalysin. Cells were transfected with CHMP2a-GFP and PM bleb formation assessed by staining non-permeabilized cells with 10 μM FM4-64. (A–C) Outlines of TR146 cells indicated by dotted lines. Scale bars represent 5 μm. (D) Confocal micrographs of TR146 cells infected with wild-type (left panel) or ece1 Δ/Δ mutant C. albicans (right panel). ALG-2 was detected by immunofluorescence. Scale bar represents 10 μm. (E) Quantification of ALG-2 accumulation as a function of invasion pocket length, from experiments like those in (D). Data are means ± SEM of ≥3 individual experiments. (F and G) Micrographs of TR146 cells treated with 30 μM candidalysin. ALG-2 (F) and ALIX (G) detected by immunofluorescence and PM blebs detected staining the PM with ConA. Images are representative of ≥3 experiments of each type. See also Figure S2 .

Article Snippet: Primary antibodies were purchased from the following vendors: anti- C. albicans (catalogue #BP1006, Acris), anti-LAMP-1 (catalogue #H4A3-s, Developmental Studies Hybridoma Bank), anti-ALIX (catalogue #ABC40, Millipore), anti-ALG-2 (catalogue #12303-1-AP, Proteintech), anti-Vinculin (catalogue #MAB3574, Millipore).

Techniques: Transfection, Staining, Infection, Mutagenesis, Immunofluorescence

Journal: Cell Reports

Article Title: Calcium-dependent ESCRT recruitment and lysosome exocytosis maintain epithelial integrity during Candida albicans invasion

doi: 10.1016/j.celrep.2021.110187

Figure Lengend Snippet:

Article Snippet: Primary antibodies were purchased from the following vendors: anti- C. albicans (catalogue #BP1006, Acris), anti-LAMP-1 (catalogue #H4A3-s, Developmental Studies Hybridoma Bank), anti-ALIX (catalogue #ABC40, Millipore), anti-ALG-2 (catalogue #12303-1-AP, Proteintech), anti-Vinculin (catalogue #MAB3574, Millipore).

Techniques: Isolation, Recombinant, Electron Microscopy, Staining, Western Blot, Plasmid Preparation, Software