Recombinant Phospho-DRP1 (Ser616) Monoclonal Antibody

SKU: AN301321L

Size::

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:Acetyl/Phospho/Methyl Antibodies;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

Isotype:IgG,κ

Clonality:Monoclonal;Recombinant

Clone NO.:8C10

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:A synthetic peptide corresponding to residues around (Ser616) of Human Phospho-DRP1

Buffer:PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant.

Purification method:Protein A

Dilution:WB 1:2000-1:10000;

Calculated MW:82 kDa

ObservedMW:82 kDa