Recombinant fosfor-DRP1 (Ser616) Monoklonale antilichamen

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.

DRP1

O00429

Human; Mouse; Rat

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

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

8C10

Unconjugated

WB

Neuroscience; Cell Biology; Signal Transduction; Metabolism; Cancer

Protein A

0.2 mg/mL

WB 1:2000-1:10000

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

Ice bag

Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.

https://789.bio/eb/L2pvPdoV

82 kDa

82 kDa

IgG, κ