Catalog_no | AP1318 |
Product_name | DRP1 (phospho-Ser616) rabbit pAb |
Category | 抗原抗体 |
Applications | WB |
Reactivity | Human |
Size | 100μg/50μg/20μg |
Price | 2200.00/1200.00/560.00 |
Gene_name | DNM1L DLP1 DRP1 |
Protein_name | DRP1 (Ser616) |
Human swiss prot no | 10059 |
Human swiss prot no | O00429 |
Mouse gene id | 74006 |
Mouse swiss prot no | Q8K1M6 |
Rat gene id | 114114 |
Rat swiss prot no | O35303 |
immunogen | Synthesized phosho peptide around human DRP1 (Ser616) |
Specificity | This antibody detects endogenous levels of Human DRP1 (phospho-Ser616) |
Formulation | Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. |
Source | Rabbit |
Dilution | WB 1:1000-2000 |
Purification | The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen. |
Concentration | 1 mg/ml |
Storage_stability | -20°C/1 year |
othername | Dynamin-1-like protein (EC 3.6.5.5) (Dnm1p/Vps1p-like protein) (DVLP) (Dynamin family member proline-rich carboxyl-terminal domain less) (Dymple) (Dynamin-like protein) (Dynamin-like protein 4) (Dynamin-like protein IV) (HdynIV) (Dynamin-related protein 1) |
Observed_band | 80KD |
Background | dynamin 1 like(DNM1L) Homo sapiens 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. [provided by RefSeq, Jun 2013], |
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