Dynamin 1-Like antibody
Quick Overview for Dynamin 1-Like antibody (ABIN7214626)
Target
See all Dynamin 1-Like (DNM1L) AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Purpose
- DRP1 Polyclonal Antibody
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Specificity
- DRP1 Polyclonal Antibody detects endogenous levels of DRP1 protein.
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Purification
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen
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Immunogen
- Synthesized peptide derived from human DRP1 around the non-phosphorylation site of S637
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Isotype
- IgG
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Application Notes
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), IHC-P (1:100-1:300), ELISA (1:10000). Not yet tested in other applications.
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Comment
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Primary Antibody
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 mg/mL
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Buffer
- PBS containing 50 % Glycerol, 0.5 % BSA and 0.02 % Sodium Azide.
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Preservative
- Sodium azide
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Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Storage
- -20 °C
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Storage Comment
- Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
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- Dynamin 1-Like (DNM1L)
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Alternative Name
- DRP1
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Background
- Rabbit Anti-DRP1 Polyclonal Antibody,DNM1L, DLP1, DRP1, Dynamin-1-like protein, 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-rela,DNM1L encodes a member of the dynamin superfamily of GTPases. Dynamin 1 like 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.,Dynamin-1-like protein
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Molecular Weight
- observerd band 80kDa
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Gene ID
- 10059
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UniProt
- O00429
Target
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