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mbp  (Miltenyi Biotec)
94
Miltenyi Biotec mbp
Antibodies for immunofluorescence staining of mouse spinal cord tissue and human tissue.
Mbp, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mbp/MBP+Antibody%2C+anti-human%2Fmouse%2C+REAfinity/pmc13693491-13-0-6
Average 94 stars, based on 1 article reviews
mbp - by Bioz Stars, 2026-11
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mouse monoclonal anti mbp antibody  (New England Biolabs)
96
New England Biolabs mouse monoclonal anti mbp antibody
Antibodies for immunofluorescence staining of mouse spinal cord tissue and human tissue.
Mouse Monoclonal Anti Mbp Antibody, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mbp/Anti-MBP+Monoclonal+Antibody/pm42883722-200-7-11
Average 96 stars, based on 1 article reviews
mouse monoclonal anti mbp antibody - by Bioz Stars, 2026-11
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mbp beads  (New England Biolabs)
99
New England Biolabs mbp beads
(A) Yeast two-hybrid (Y2H) assay of UBP12/13 and CaMV proteins. Yeast co-transformants grown on nonselective media (-Leu/-Trp) and selective media (-Leu/-Trp/-His/-Ade) were shown. Vet.: empty vector. SD/-L.T indicates Leu and Trp drop-out medium. SD/-L.T.H.A indicates Leu, Trp, His and Ade drop-out medium. (B) In vitro pull-down assay shows a direct interaction between <t>GST-UBP12/13</t> and <t>MBP-P6.</t> GST-UBP12, GST-UBP13 and GST (negative control) were used as baits. MBP-P6 were used as target protein. G: GST. (C) Co-immunoprecipitation (Co-IP) assay for detecting the interaction between UBP12/13 and P6 using transgenic Arabidopsis co-expressing P6 and UBP12/13. Extracts were immunoprecipitated with anti-FLAG antibody and anti-IgG antibody (negative control). Immunoprecipitates were then analyzed by immunoblotting assay using anti-GFP and anti-FLAG antibody. Input controls were shown. (D) Bimolecular fluorescence complementation (BiFC) assays between UBP12/13 and P6 in Arabidopsis protoplasts. Confocal imaging was performed at 12 h post inoculation. UBP12/13 and P6 were fused to nEYFP and cEYFP, respectively. mCherry-VirD2NLS was co-expressed as a nuclear marker. Bar, 5 μm.
Mbp Beads, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mbp/Amylose+Resin/pmc13690193-203-0-2
Average 99 stars, based on 1 article reviews
mbp beads - by Bioz Stars, 2026-11
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rat mbp  (Novus Biologicals)
94
Novus Biologicals rat mbp
(A) Yeast two-hybrid (Y2H) assay of UBP12/13 and CaMV proteins. Yeast co-transformants grown on nonselective media (-Leu/-Trp) and selective media (-Leu/-Trp/-His/-Ade) were shown. Vet.: empty vector. SD/-L.T indicates Leu and Trp drop-out medium. SD/-L.T.H.A indicates Leu, Trp, His and Ade drop-out medium. (B) In vitro pull-down assay shows a direct interaction between <t>GST-UBP12/13</t> and <t>MBP-P6.</t> GST-UBP12, GST-UBP13 and GST (negative control) were used as baits. MBP-P6 were used as target protein. G: GST. (C) Co-immunoprecipitation (Co-IP) assay for detecting the interaction between UBP12/13 and P6 using transgenic Arabidopsis co-expressing P6 and UBP12/13. Extracts were immunoprecipitated with anti-FLAG antibody and anti-IgG antibody (negative control). Immunoprecipitates were then analyzed by immunoblotting assay using anti-GFP and anti-FLAG antibody. Input controls were shown. (D) Bimolecular fluorescence complementation (BiFC) assays between UBP12/13 and P6 in Arabidopsis protoplasts. Confocal imaging was performed at 12 h post inoculation. UBP12/13 and P6 were fused to nEYFP and cEYFP, respectively. mCherry-VirD2NLS was co-expressed as a nuclear marker. Bar, 5 μm.
Rat Mbp, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mbp/Rat+MBP+ELISA+Kit+(Colorimetric)/pm42866172-92-25-28
Average 94 stars, based on 1 article reviews
rat mbp - by Bioz Stars, 2026-11
94/100 stars
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construct encoding nanoluc luciferase nluc  (Addgene inc)
94
Addgene inc construct encoding nanoluc luciferase nluc
(A) Yeast two-hybrid (Y2H) assay of UBP12/13 and CaMV proteins. Yeast co-transformants grown on nonselective media (-Leu/-Trp) and selective media (-Leu/-Trp/-His/-Ade) were shown. Vet.: empty vector. SD/-L.T indicates Leu and Trp drop-out medium. SD/-L.T.H.A indicates Leu, Trp, His and Ade drop-out medium. (B) In vitro pull-down assay shows a direct interaction between <t>GST-UBP12/13</t> and <t>MBP-P6.</t> GST-UBP12, GST-UBP13 and GST (negative control) were used as baits. MBP-P6 were used as target protein. G: GST. (C) Co-immunoprecipitation (Co-IP) assay for detecting the interaction between UBP12/13 and P6 using transgenic Arabidopsis co-expressing P6 and UBP12/13. Extracts were immunoprecipitated with anti-FLAG antibody and anti-IgG antibody (negative control). Immunoprecipitates were then analyzed by immunoblotting assay using anti-GFP and anti-FLAG antibody. Input controls were shown. (D) Bimolecular fluorescence complementation (BiFC) assays between UBP12/13 and P6 in Arabidopsis protoplasts. Confocal imaging was performed at 12 h post inoculation. UBP12/13 and P6 were fused to nEYFP and cEYFP, respectively. mCherry-VirD2NLS was co-expressed as a nuclear marker. Bar, 5 μm.
Construct Encoding Nanoluc Luciferase Nluc, supplied by Addgene inc, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mbp/pET20b-NLuc-MBP-6xHis+(Plasmid+%23135931)/pm42869022-943-1-9
Average 94 stars, based on 1 article reviews
construct encoding nanoluc luciferase nluc - by Bioz Stars, 2026-11
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myelin basic protein antibody / mbp  (NSJ Bioreagents)
93
NSJ Bioreagents myelin basic protein antibody / mbp
(A) Yeast two-hybrid (Y2H) assay of UBP12/13 and CaMV proteins. Yeast co-transformants grown on nonselective media (-Leu/-Trp) and selective media (-Leu/-Trp/-His/-Ade) were shown. Vet.: empty vector. SD/-L.T indicates Leu and Trp drop-out medium. SD/-L.T.H.A indicates Leu, Trp, His and Ade drop-out medium. (B) In vitro pull-down assay shows a direct interaction between <t>GST-UBP12/13</t> and <t>MBP-P6.</t> GST-UBP12, GST-UBP13 and GST (negative control) were used as baits. MBP-P6 were used as target protein. G: GST. (C) Co-immunoprecipitation (Co-IP) assay for detecting the interaction between UBP12/13 and P6 using transgenic Arabidopsis co-expressing P6 and UBP12/13. Extracts were immunoprecipitated with anti-FLAG antibody and anti-IgG antibody (negative control). Immunoprecipitates were then analyzed by immunoblotting assay using anti-GFP and anti-FLAG antibody. Input controls were shown. (D) Bimolecular fluorescence complementation (BiFC) assays between UBP12/13 and P6 in Arabidopsis protoplasts. Confocal imaging was performed at 12 h post inoculation. UBP12/13 and P6 were fused to nEYFP and cEYFP, respectively. mCherry-VirD2NLS was co-expressed as a nuclear marker. Bar, 5 μm.
Myelin Basic Protein Antibody / Mbp, supplied by NSJ Bioreagents, 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/product/mbp/Myelin+Basic+Protein+Antibody+%2F+MBP/custom%40rq5003%4010%2E1186%2Fs12974-026-04075-9
Average 93 stars, based on 1 article reviews
myelin basic protein antibody / mbp - by Bioz Stars, 2026-11
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mbp monoclonal antibody  (New England Biolabs)
96
New England Biolabs mbp monoclonal antibody
(A) Yeast two-hybrid (Y2H) assay of UBP12/13 and CaMV proteins. Yeast co-transformants grown on nonselective media (-Leu/-Trp) and selective media (-Leu/-Trp/-His/-Ade) were shown. Vet.: empty vector. SD/-L.T indicates Leu and Trp drop-out medium. SD/-L.T.H.A indicates Leu, Trp, His and Ade drop-out medium. (B) In vitro pull-down assay shows a direct interaction between <t>GST-UBP12/13</t> and <t>MBP-P6.</t> GST-UBP12, GST-UBP13 and GST (negative control) were used as baits. MBP-P6 were used as target protein. G: GST. (C) Co-immunoprecipitation (Co-IP) assay for detecting the interaction between UBP12/13 and P6 using transgenic Arabidopsis co-expressing P6 and UBP12/13. Extracts were immunoprecipitated with anti-FLAG antibody and anti-IgG antibody (negative control). Immunoprecipitates were then analyzed by immunoblotting assay using anti-GFP and anti-FLAG antibody. Input controls were shown. (D) Bimolecular fluorescence complementation (BiFC) assays between UBP12/13 and P6 in Arabidopsis protoplasts. Confocal imaging was performed at 12 h post inoculation. UBP12/13 and P6 were fused to nEYFP and cEYFP, respectively. mCherry-VirD2NLS was co-expressed as a nuclear marker. Bar, 5 μm.
Mbp Monoclonal Antibody, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mbp/Anti-MBP+Monoclonal+Antibody/bio_rxiv__64898__2026__10__09__758143-272-17-20
Average 96 stars, based on 1 article reviews
mbp monoclonal antibody - by Bioz Stars, 2026-11
96/100 stars
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mbp  (Proteintech)
96
Proteintech mbp
(A) Yeast two-hybrid (Y2H) assay of UBP12/13 and CaMV proteins. Yeast co-transformants grown on nonselective media (-Leu/-Trp) and selective media (-Leu/-Trp/-His/-Ade) were shown. Vet.: empty vector. SD/-L.T indicates Leu and Trp drop-out medium. SD/-L.T.H.A indicates Leu, Trp, His and Ade drop-out medium. (B) In vitro pull-down assay shows a direct interaction between <t>GST-UBP12/13</t> and <t>MBP-P6.</t> GST-UBP12, GST-UBP13 and GST (negative control) were used as baits. MBP-P6 were used as target protein. G: GST. (C) Co-immunoprecipitation (Co-IP) assay for detecting the interaction between UBP12/13 and P6 using transgenic Arabidopsis co-expressing P6 and UBP12/13. Extracts were immunoprecipitated with anti-FLAG antibody and anti-IgG antibody (negative control). Immunoprecipitates were then analyzed by immunoblotting assay using anti-GFP and anti-FLAG antibody. Input controls were shown. (D) Bimolecular fluorescence complementation (BiFC) assays between UBP12/13 and P6 in Arabidopsis protoplasts. Confocal imaging was performed at 12 h post inoculation. UBP12/13 and P6 were fused to nEYFP and cEYFP, respectively. mCherry-VirD2NLS was co-expressed as a nuclear marker. Bar, 5 μm.
Mbp, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mbp/IkB+alpha+Polyclonal+antibody/10__1096_slash_fj__202601940r-104-49-50
Average 96 stars, based on 1 article reviews
mbp - by Bioz Stars, 2026-11
96/100 stars
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his6 mbp utev3 plasmid  (Addgene inc)
94
Addgene inc his6 mbp utev3 plasmid
(A) Yeast two-hybrid (Y2H) assay of UBP12/13 and CaMV proteins. Yeast co-transformants grown on nonselective media (-Leu/-Trp) and selective media (-Leu/-Trp/-His/-Ade) were shown. Vet.: empty vector. SD/-L.T indicates Leu and Trp drop-out medium. SD/-L.T.H.A indicates Leu, Trp, His and Ade drop-out medium. (B) In vitro pull-down assay shows a direct interaction between <t>GST-UBP12/13</t> and <t>MBP-P6.</t> GST-UBP12, GST-UBP13 and GST (negative control) were used as baits. MBP-P6 were used as target protein. G: GST. (C) Co-immunoprecipitation (Co-IP) assay for detecting the interaction between UBP12/13 and P6 using transgenic Arabidopsis co-expressing P6 and UBP12/13. Extracts were immunoprecipitated with anti-FLAG antibody and anti-IgG antibody (negative control). Immunoprecipitates were then analyzed by immunoblotting assay using anti-GFP and anti-FLAG antibody. Input controls were shown. (D) Bimolecular fluorescence complementation (BiFC) assays between UBP12/13 and P6 in Arabidopsis protoplasts. Confocal imaging was performed at 12 h post inoculation. UBP12/13 and P6 were fused to nEYFP and cEYFP, respectively. mCherry-VirD2NLS was co-expressed as a nuclear marker. Bar, 5 μm.
His6 Mbp Utev3 Plasmid, supplied by Addgene inc, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mbp/His6-MBP-uTEV3+(Plasmid+%23135464)/10__1038_slash_s41467___026___77990___3-321-12-14
Average 94 stars, based on 1 article reviews
his6 mbp utev3 plasmid - by Bioz Stars, 2026-11
94/100 stars
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mbp trap hp column  (Cytiva Europe)
95
Cytiva Europe mbp trap hp column
(A) Yeast two-hybrid (Y2H) assay of UBP12/13 and CaMV proteins. Yeast co-transformants grown on nonselective media (-Leu/-Trp) and selective media (-Leu/-Trp/-His/-Ade) were shown. Vet.: empty vector. SD/-L.T indicates Leu and Trp drop-out medium. SD/-L.T.H.A indicates Leu, Trp, His and Ade drop-out medium. (B) In vitro pull-down assay shows a direct interaction between <t>GST-UBP12/13</t> and <t>MBP-P6.</t> GST-UBP12, GST-UBP13 and GST (negative control) were used as baits. MBP-P6 were used as target protein. G: GST. (C) Co-immunoprecipitation (Co-IP) assay for detecting the interaction between UBP12/13 and P6 using transgenic Arabidopsis co-expressing P6 and UBP12/13. Extracts were immunoprecipitated with anti-FLAG antibody and anti-IgG antibody (negative control). Immunoprecipitates were then analyzed by immunoblotting assay using anti-GFP and anti-FLAG antibody. Input controls were shown. (D) Bimolecular fluorescence complementation (BiFC) assays between UBP12/13 and P6 in Arabidopsis protoplasts. Confocal imaging was performed at 12 h post inoculation. UBP12/13 and P6 were fused to nEYFP and cEYFP, respectively. mCherry-VirD2NLS was co-expressed as a nuclear marker. Bar, 5 μm.
Mbp Trap Hp Column, supplied by Cytiva Europe, 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/mbp/MBPTrap+HP+column/pm42844479-827-8-12
Average 95 stars, based on 1 article reviews
mbp trap hp column - by Bioz Stars, 2026-11
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Image Search Results


Antibodies for immunofluorescence staining of mouse spinal cord tissue and human tissue.

Journal: Glia

Article Title: Astrocytic EAAT ‐2 Upregulation Supports Neuro‐Axonal Homeostasis in Chronic Inflammatory CNS Lesions

doi: 10.1002/glia.70243

Figure Lengend Snippet: Antibodies for immunofluorescence staining of mouse spinal cord tissue and human tissue.

Article Snippet: MBP , PE , REA1154 , Miltenyi Biotec , 130‐120‐342 , Human cell line , Hu, ms, rat , 1:50.

Techniques: Immunofluorescence, Staining, Tissue

(A) Yeast two-hybrid (Y2H) assay of UBP12/13 and CaMV proteins. Yeast co-transformants grown on nonselective media (-Leu/-Trp) and selective media (-Leu/-Trp/-His/-Ade) were shown. Vet.: empty vector. SD/-L.T indicates Leu and Trp drop-out medium. SD/-L.T.H.A indicates Leu, Trp, His and Ade drop-out medium. (B) In vitro pull-down assay shows a direct interaction between GST-UBP12/13 and MBP-P6. GST-UBP12, GST-UBP13 and GST (negative control) were used as baits. MBP-P6 were used as target protein. G: GST. (C) Co-immunoprecipitation (Co-IP) assay for detecting the interaction between UBP12/13 and P6 using transgenic Arabidopsis co-expressing P6 and UBP12/13. Extracts were immunoprecipitated with anti-FLAG antibody and anti-IgG antibody (negative control). Immunoprecipitates were then analyzed by immunoblotting assay using anti-GFP and anti-FLAG antibody. Input controls were shown. (D) Bimolecular fluorescence complementation (BiFC) assays between UBP12/13 and P6 in Arabidopsis protoplasts. Confocal imaging was performed at 12 h post inoculation. UBP12/13 and P6 were fused to nEYFP and cEYFP, respectively. mCherry-VirD2NLS was co-expressed as a nuclear marker. Bar, 5 μm.

Journal: PLOS Pathogens

Article Title: The pathogenicity factor of DNA virus interacts with Arabidopsis deubiquitinases UBP12/13 to promote viral infection

doi: 10.1371/journal.ppat.1014686

Figure Lengend Snippet: (A) Yeast two-hybrid (Y2H) assay of UBP12/13 and CaMV proteins. Yeast co-transformants grown on nonselective media (-Leu/-Trp) and selective media (-Leu/-Trp/-His/-Ade) were shown. Vet.: empty vector. SD/-L.T indicates Leu and Trp drop-out medium. SD/-L.T.H.A indicates Leu, Trp, His and Ade drop-out medium. (B) In vitro pull-down assay shows a direct interaction between GST-UBP12/13 and MBP-P6. GST-UBP12, GST-UBP13 and GST (negative control) were used as baits. MBP-P6 were used as target protein. G: GST. (C) Co-immunoprecipitation (Co-IP) assay for detecting the interaction between UBP12/13 and P6 using transgenic Arabidopsis co-expressing P6 and UBP12/13. Extracts were immunoprecipitated with anti-FLAG antibody and anti-IgG antibody (negative control). Immunoprecipitates were then analyzed by immunoblotting assay using anti-GFP and anti-FLAG antibody. Input controls were shown. (D) Bimolecular fluorescence complementation (BiFC) assays between UBP12/13 and P6 in Arabidopsis protoplasts. Confocal imaging was performed at 12 h post inoculation. UBP12/13 and P6 were fused to nEYFP and cEYFP, respectively. mCherry-VirD2NLS was co-expressed as a nuclear marker. Bar, 5 μm.

Article Snippet: MBP beads (NEB, Cat. No. E8021S) and GST beads (GE Healthcare, Cat. No. 17-0756-01) were used to purify the MBP-fusion proteins and GST-fusion proteins, respectively.

Techniques: Yeast, Y2H Assay, Plasmid Preparation, In Vitro, Pull Down Assay, Negative Control, Co-Immunoprecipitation Assay, Transgenic Assay, Expressing, Immunoprecipitation, Western Blot, Fluorescence, Confocal, Imaging, Marker

(A) In vitro pull-down assay shows a direct interaction between GST-UBP12/13 and MBP-AC2. GST-UBP12, GST-UBP13 and GST (control) were used as baits. MBP-AC2 was used as the target protein. G: GST. (B) Co-immunoprecipitation (Co-IP) assay for detecting the interaction between AC2 and UBP12/13 using the transgenic Arabidopsis co-expressing AC2 and UBP12/13. Extracts were immunoprecipitated with anti-FLAG antibody and anti-IgG antibody. Immunoprecipitates were then analyzed by immunoblotting assay using anti-MYC and anti-FLAG antibody. Input proteins were shown. (C) BiFC assays between UBP12/13 and AC2 in N. benthamiana . Confocal images were taken 2 days after infiltration. UBP12/13 and AC2 were respectively fused to nEYFP and cEYFP. H2B-mCherry was as a nuclear protein marker. Bar, 20 μm.

Journal: PLOS Pathogens

Article Title: The pathogenicity factor of DNA virus interacts with Arabidopsis deubiquitinases UBP12/13 to promote viral infection

doi: 10.1371/journal.ppat.1014686

Figure Lengend Snippet: (A) In vitro pull-down assay shows a direct interaction between GST-UBP12/13 and MBP-AC2. GST-UBP12, GST-UBP13 and GST (control) were used as baits. MBP-AC2 was used as the target protein. G: GST. (B) Co-immunoprecipitation (Co-IP) assay for detecting the interaction between AC2 and UBP12/13 using the transgenic Arabidopsis co-expressing AC2 and UBP12/13. Extracts were immunoprecipitated with anti-FLAG antibody and anti-IgG antibody. Immunoprecipitates were then analyzed by immunoblotting assay using anti-MYC and anti-FLAG antibody. Input proteins were shown. (C) BiFC assays between UBP12/13 and AC2 in N. benthamiana . Confocal images were taken 2 days after infiltration. UBP12/13 and AC2 were respectively fused to nEYFP and cEYFP. H2B-mCherry was as a nuclear protein marker. Bar, 20 μm.

Article Snippet: MBP beads (NEB, Cat. No. E8021S) and GST beads (GE Healthcare, Cat. No. 17-0756-01) were used to purify the MBP-fusion proteins and GST-fusion proteins, respectively.

Techniques: In Vitro, Pull Down Assay, Control, Co-Immunoprecipitation Assay, Transgenic Assay, Expressing, Immunoprecipitation, Western Blot, Confocal, Marker