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Products:Neuroscience >> Neurology process >> Neurodegenerative disease >> Parkinson's disease >> Synuclein
MSCatalog No. MS764
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Read our guarantee »Anti-VCP antibody [3E8DC11 ]
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Mouse monoclonal [3E8DC11 ] to VCP
In-Cell ELISA, ICC/IF, Flow Cyt, IPmore details
Reacts with
Mouse, Rat, Human
Sucrose gradient fraction 4 from Human liver mitochondria.
ICC/IF: Human HDFn cells IP: Human, Rat, and Mouse liver samples; HepG2 cultured cell lysate Flow Cyt: HL-60 cells
Liquid
Store at +4°C. Do not freeze.
Preservative: 0.02% Sodium azide
Concentration information loading...
>95% by SDS-PAGE
The purity of ab110308 is near homogeneity, as judged by SDS-PAGE. The antibody was produced in vitro using hybridomas grown in serum-free medium, and then purified by biochemical fractionation.
Monoclonal
3E8DC11
IgG1
kappa
Our Abpromise guarantee covers the use of ab110308 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
In-Cell ELISA: Use a concentration of 2 µg/ml. (0.2 µg/well)
ICC/IF: Use a concentration of 2 µg/ml.
Flow Cyt: Use a concentration of 1 µg/ml.
IP: Use at an assay dependent dilution.
Necessary for the fragmentation of Golgi stacks during mitosis and for their reassembly after mitosis. Involved in the formation of the transitional endoplasmic reticulum (tER). The transfer of membranes from the endoplasmic reticulum to the Golgi apparatus occurs via 50-70 nm transition vesicles which derive from part-rough, part-smooth transitional elements of the endoplasmic reticulum (tER). Vesicle budding from the tER is an ATP-dependent process. The ternary complex containing UFD1L, VCP and NPLOC4 binds ubiquitinated proteins and is necessary for the export of misfolded proteins from the ER to the cytoplasm, where they are degraded by the proteasome. The NPLOC4-UFD1L-VCP complex regulates spindle disassembly at the end of mitosis and is necessary for the formation of a closed nuclear envelope (By similarity). Regulates E3 ubiquitin-protein ligase activity of RNF19A.
Defects in VCP are the cause of inclusion body myopathy with early-onset Paget disease and frontotemporal dementia (IBMPFD) [MIM:167320]; also known as muscular dystrophy, limb-girdle, with Paget disease of bone or pagetoid amyotrophic lateral sclerosis or pagetoid neuroskeletal syndrome or lower motor neuron degeneration with Paget-like bone disease. IBMPFD features adult-onset proximal and distal muscle weakness (clinically resembling limb girdle muscular dystrophy), early-onset Paget disease of bone in most cases and premature frontotemporal dementia.
Belongs to the AAA ATPase family.
Phosphorylated by tyrosine kinases in response to T-cell antigen receptor activation (By similarity). Phosphorylated upon DNA damage, probably by ATM or ATR.
ISGylated.
Cytoplasm > cytosol. Nucleus. Present in the neuronal hyaline inclusion bodies specifically found in motor neurons from amyotrophic lateral sclerosis patients. Present in the Lewy bodies specifically found in neurons from Parkinson disease patients.
Target information above from: UniProt accessionP55072
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Immunocytochemistry/ Immunofluorescence - VCP antibody [3E8DC11 ] (ab110308)
![Immunocytochemistry/ Immunofluorescence - VCP antibody [3E8DC11 ] (ab110308)](/ps/datasheet/images/110/ab110308/VCP-Primary-antibodies-ab110308-1.jpg)
Immunocytochemistry image of ab110308-stained Human HDFn cells. The cells were paraformaldehyde fixed (4%, 20 min) and Triton X-100 permeabilized (0.1%, 15 min). The cells were incubated with ab110308 at 2 µg/ml) for 2 hours at room temperature or over night at 4°C. The secondary antibody was (green) Alexa Fluor® 488 goat anti-mouse IgG (H+L) used at a 1/1000 dilution for 1 hour. 10% Goat serum was used as the blocking agent for all blocking steps. Target protein locates mainly in nucleus and cytoplasm.
Immunoprecipitation - VCP antibody [3E8DC11 ] (ab110308)
![Immunoprecipitation - VCP antibody [3E8DC11 ] (ab110308)](/ps/datasheet/images/110/ab110308/VCP-Primary-antibodies-ab110308-2.jpg)
ab110308 pulls down the 89 kDa VCP protein in Human (lane 1), Rat (lane 2), and Mouse (lane 3) liver samples and Human HepG2 cultured cell lysate (lane 4). The identity of this protein was confirmed by mass spectrometry. This gel was stained with sypro ruby gel stain.
Flow Cytometry - VCP antibody [3E8DC11 ] (ab110308)
![Flow Cytometry - VCP antibody [3E8DC11 ] (ab110308)](/ps/datasheet/images/110/ab110308/VCP-Primary-antibodies-ab110308-3.jpg)
HL-60 cells were stained with 1 µg/mL ab110308 (blue) or an equal amount of an isotype control antibody (red) and analyzed by flow cytometry.
ab110308 has not yet been referenced specifically in any publications.
Publishing research using ab110308? Please let us know so that we can cite the reference in this datasheet
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![Immunocytochemistry/ Immunofluorescence - VCP antibody [3E8DC11 ] (ab110308)](/ps/datasheet/images/110/ab110308/VCP-Primary-antibodies-ab110308-1.jpg)
Immunocytochemistry image of ab110308-stained Human HDFn cells. The cells were paraformaldehyde fixed (4%, 20 min) and Triton X-100 permeabilized (0.1%, 15 min). The cells were incubated with ab110308 at 2 µg/ml) for 2 hours at room temperature or over night at 4°C. The secondary antibody was (green) Alexa Fluor® 488 goat anti-mouse IgG (H+L) used at a 1/1000 dilution for 1 hour. 10% Goat serum was used as the blocking agent for all blocking steps. Target protein locates mainly in nucleus and cytoplasm.
![Immunoprecipitation - VCP antibody [3E8DC11 ] (ab110308)](/ps/datasheet/images/110/ab110308/VCP-Primary-antibodies-ab110308-2.jpg)
ab110308 pulls down the 89 kDa VCP protein in Human (lane 1), Rat (lane 2), and Mouse (lane 3) liver samples and Human HepG2 cultured cell lysate (lane 4). The identity of this protein was confirmed by mass spectrometry. This gel was stained with sypro ruby gel stain.
![Flow Cytometry - VCP antibody [3E8DC11 ] (ab110308)](/ps/datasheet/images/110/ab110308/VCP-Primary-antibodies-ab110308-3.jpg)
HL-60 cells were stained with 1 µg/mL ab110308 (blue) or an equal amount of an isotype control antibody (red) and analyzed by flow cytometry.
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