vdac n152b Search Results


anti-vdac1  (Developmental Studies Hybridoma Bank)
N/A
VDAC1
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mouse vdac1 monoclonal antibody  (NeuroMab)
94
NeuroMab mouse vdac1 monoclonal antibody
(A and B) Wild-type (A) and GFP-tagged (B) human Mtln were expressed in neonatal rat cardiomyocytes, and co-localization with MitoTracker red was evaluated. Representative photomicrographs are shown. Scale bars, 10 μm. (C) Mitochondrial pellets were isolated from wild-type (WT) or Mtln-knockout (KO) C2C12 myoblast cells, and western blot was performed on various fractions. (D) Mitochondrial pellets harvested from WT or Mtln-KO skeletal muscle tissues were treated with increasing digitonin concentrations to release OMMs, and pellet and supernatant fraction fractions were subjected to western blot analysis. Cox4 and <t>Vdac1</t> are known IMM and OMM proteins, respectively. Gapdh is a cytosolic protein known to associate with mitochondria in some cases. (E) Mitochondrial pellets harvested from WT skeletal muscle tissues were resuspended in isotonic, hypotonic, or isotonic plus triton buffers in the absence or presence of proteinase K and subjected to western blot analysis. Proteins with known localization to various mitochondrial compartments (e.g., matrix, IMM, and intermembrane space [IMS]) were evaluated as controls. (F) Western blot analysis performed on WT and Mtln-KO cardiac tissue lysates subjected to pull-down assay using cardiolipin (CL)-coated or control beads. Subunit c, a known cardiolipin-binding protein, serves as the positive control. (G) Lipid-strip binding assay performed using synthetic Mtln protein followed by anti-Mtln immunoblot.
Mouse Vdac1 Monoclonal Antibody, supplied by NeuroMab, 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/vdac+n152b/Anti-VDAC1+Antibody/pmc06091870-3-0-6
Average 94 stars, based on 1 article reviews
mouse vdac1 monoclonal antibody - by Bioz Stars, 2026-09
94/100 stars
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anti-vdac1 antibody  (NeuroMab)
N/A
Our carrier-free Anti-VDAC1 mouse monoclonal primary antibody from NeuroMab is produced in-house from hybridoma clone N152B/23. It is KO validated, detects human, mouse, and rat VDAC1, and is purified by Protein A chromatography. It is
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anti-vdac1 antibody fl550 conjugate  (NeuroMab)
N/A
Our Anti-VDAC1 mouse monoclonal primary antibody from NeuroMab is produced in-house from hybridoma clone N152B/23. It is KO validated, detects human, mouse, and rat VDAC1, and is purified by Protein A chromatography. It is great
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vdac1 mouse monoclonal antibody  (OriGene)
N/A
VDAC1 mouse monoclonal antibody clone N152B 23
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anti-vdac1 antibody fl594 conjugate  (NeuroMab)
N/A
Our Anti-VDAC1 mouse monoclonal primary antibody from NeuroMab is produced in-house from hybridoma clone N152B/23. It is KO validated, detects human, mouse, and rat VDAC1, and is purified by Protein A chromatography. It is great
   Buy from Supplier
anti-vdac1 antibody fl490 conjugate  (NeuroMab)
N/A
Our Anti-VDAC1 mouse monoclonal primary antibody from NeuroMab is produced in-house from hybridoma clone N152B/23. It is KO validated, detects human, mouse, and rat VDAC1, and is purified by Protein A chromatography. It is great
   Buy from Supplier
anti-vdac1 antibody fl650 conjugate  (NeuroMab)
N/A
Our Anti-VDAC1 mouse monoclonal primary antibody from NeuroMab is produced in-house from hybridoma clone N152B/23. It is KO validated, detects human, mouse, and rat VDAC1, and is purified by Protein A chromatography. It is great
   Buy from Supplier
purified anti-vdac1  (BioLegend)
N/A
Purified anti-VDAC1 [N152B/23]; Isotype: Mouse IgG2a; Reactivity: Human, Mouse, Rat; Apps: WB, IHC; Size: 100 μl
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Image Search Results


(A and B) Wild-type (A) and GFP-tagged (B) human Mtln were expressed in neonatal rat cardiomyocytes, and co-localization with MitoTracker red was evaluated. Representative photomicrographs are shown. Scale bars, 10 μm. (C) Mitochondrial pellets were isolated from wild-type (WT) or Mtln-knockout (KO) C2C12 myoblast cells, and western blot was performed on various fractions. (D) Mitochondrial pellets harvested from WT or Mtln-KO skeletal muscle tissues were treated with increasing digitonin concentrations to release OMMs, and pellet and supernatant fraction fractions were subjected to western blot analysis. Cox4 and Vdac1 are known IMM and OMM proteins, respectively. Gapdh is a cytosolic protein known to associate with mitochondria in some cases. (E) Mitochondrial pellets harvested from WT skeletal muscle tissues were resuspended in isotonic, hypotonic, or isotonic plus triton buffers in the absence or presence of proteinase K and subjected to western blot analysis. Proteins with known localization to various mitochondrial compartments (e.g., matrix, IMM, and intermembrane space [IMS]) were evaluated as controls. (F) Western blot analysis performed on WT and Mtln-KO cardiac tissue lysates subjected to pull-down assay using cardiolipin (CL)-coated or control beads. Subunit c, a known cardiolipin-binding protein, serves as the positive control. (G) Lipid-strip binding assay performed using synthetic Mtln protein followed by anti-Mtln immunoblot.

Journal: Cell reports

Article Title: Mitoregulin: A lncRNA-Encoded Microprotein that Supports Mitochondrial Supercomplexes and Respiratory Efficiency

doi: 10.1016/j.celrep.2018.06.002

Figure Lengend Snippet: (A and B) Wild-type (A) and GFP-tagged (B) human Mtln were expressed in neonatal rat cardiomyocytes, and co-localization with MitoTracker red was evaluated. Representative photomicrographs are shown. Scale bars, 10 μm. (C) Mitochondrial pellets were isolated from wild-type (WT) or Mtln-knockout (KO) C2C12 myoblast cells, and western blot was performed on various fractions. (D) Mitochondrial pellets harvested from WT or Mtln-KO skeletal muscle tissues were treated with increasing digitonin concentrations to release OMMs, and pellet and supernatant fraction fractions were subjected to western blot analysis. Cox4 and Vdac1 are known IMM and OMM proteins, respectively. Gapdh is a cytosolic protein known to associate with mitochondria in some cases. (E) Mitochondrial pellets harvested from WT skeletal muscle tissues were resuspended in isotonic, hypotonic, or isotonic plus triton buffers in the absence or presence of proteinase K and subjected to western blot analysis. Proteins with known localization to various mitochondrial compartments (e.g., matrix, IMM, and intermembrane space [IMS]) were evaluated as controls. (F) Western blot analysis performed on WT and Mtln-KO cardiac tissue lysates subjected to pull-down assay using cardiolipin (CL)-coated or control beads. Subunit c, a known cardiolipin-binding protein, serves as the positive control. (G) Lipid-strip binding assay performed using synthetic Mtln protein followed by anti-Mtln immunoblot.

Article Snippet: Mouse VDAC1 monoclonal antibody (N152B/23) , NeuroMab , Cat# 75–204; RRID: AB_2214807.

Techniques: Isolation, Knock-Out, Western Blot, Pull Down Assay, Control, Binding Assay, Positive Control, Stripping Membranes

Journal: Cell reports

Article Title: Mitoregulin: A lncRNA-Encoded Microprotein that Supports Mitochondrial Supercomplexes and Respiratory Efficiency

doi: 10.1016/j.celrep.2018.06.002

Figure Lengend Snippet:

Article Snippet: Mouse VDAC1 monoclonal antibody (N152B/23) , NeuroMab , Cat# 75–204; RRID: AB_2214807.

Techniques: Recombinant, Isolation, Control, Glutathione Assay, Bioassay, Knock-Out, Negative Control, Multiplex Assay, CRISPR, Plasmid Preparation, Software