Recombinatie DRp1 monoklonaal antilichaam

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

Recombinant Human DRP1 protein

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

2C6

Unconjugated

WB; IHC

Neuroscience; Cell Biology; Signal Transduction; Metabolism; Cancer

Protein A

0.2 mg/mL

IHC 1:200-1000; WB 1:1000-5000

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/0uf0C7Hc

83 kDa

83 kDa

IgG, κ