GeneBio Systems
Recombinant DRP1 Monoclonal Antibody
Recombinant DRP1 Monoclonal Antibody
SKU:AN301080L
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Size::50μL
Storage:Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.
Shipping:Ice bag
Exp date:12 months
Category ID_II:Primary Antibodies
Category ID_III:Recombinant Antibodies;Monoclonal Antibodies
Abbreviation:DRP1
Target Synonym:DRP;DLP;DNM1L;DLP1;DRP1;DVLP;DYMPLE;EMPF;EMPF1;HDYNIV;Dnm1p/Vps1p-like protein (DVLP);dynamin 1 like;Dynamin family member proline-rich carboxyl-terminal domain less (Dymple);Dynamin-1-like protein;Dynamin-like protein;DLP1;DRP1;DVLP;DYMPLE;dynamin 1 like;EMPF;EMPF1;HDYNIV;Dnm1p/Vps1p-like protein;dnml1;Dynamin family member proline-rich carboxyl-terminal domain less;Dynamin like protein;Dynamin related protein 1;Dynamin-like protein 4;Dynamin-like protein IV;Dynamin-related protein 1;DYNIV 11;FLJ41912;VPS1
Research Areas:Neuroscience;Cell Biology;Signal Transduction;Metabolism;Cancer
Conjugation:Unconjugated
Host:Rabbit
Species reactivity:Human;Mouse;Rat
Application:WB;IHC
Isotype:IgG,κ
Clonality:Monoclonal;Recombinant
Clone NO.:2C6
UNIProt ID:O00429
Accession:
Background:This gene encodes a member of the dynamin superfamily of GTPases. The encoded protein mediates mitochondrial and peroxisomal division, and is involved in developmentally regulated apoptosis and programmed necrosis. Dysfunction of this gene is implicated in several neurological disorders, including Alzheimer's disease. Mutations in this gene are associated with the autosomal dominant disorder, encephalopathy, lethal, due to defective mitochondrial and peroxisomal fission (EMPF). Alternative splicing results in multiple transcript variants encoding different isoforms.
Concentration:0.2 mg/mL
Immunogen:Recombinant Human DRP1 protein
Buffer:PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant.
Purification method:Protein A
Dilution:IHC 1:200-1000;WB 1:1000-5000
Calculated MW:83 kDa
ObservedMW:83 kDa
