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Anti-DRP1 Antibody

品牌：Antibodies

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規(guī)格：50μl

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Anti-DRP1 Antibody

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Overview

Name:	Anti-DRP1 Antibody See all DRP1 primary antibodies
Description:	Rabbit polyclonal antibody to DRP1
Specificity:	DRP1 Polyclonal Antibody detects endogenous levels of DRP1 protein.
Applications:	WB, IHC, ELISA
Reactivity:	Human, Mouse, Rat
Immunogen:	Synthesized peptide derived from human DRP1 around the non-phosphorylation site of S637.
Host:	Rabbit
Clonality:	Polyclonal
Conjugate:	Unconjugated
Purification:	The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration:	1mg / ml
Formulation:	Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Storage:	Store at -20?C / 1 year

Target

Function:	Functions in mitochondrial and peroxisomal division. Mediates membrane fission through oligomerization into membrane-associated tubular structures that wrap around the scission site to constrict and sever the mitochondrial membrane through a GTP hydrolysis-dependent mechanism. Through its function in mitochondrial division, ensures the survival of at least some types of postmitotic neurons, including Purkinje cells, by suppressing oxidative damage. Required for normal brain development, including that of cerebellum. Facilitates developmentally regulated apoptosis during neural tube formation. Required for a normal rate of cytochrome c release and caspase activation during apoptosis; this requirement may depend upon the cell type and the physiological apoptotic cues. Plays an important role in mitochondrial fission during mitosis (PubMed:26992161). Required for formation of endocytic vesicles. Proposed to regulate synaptic vesicle membrane dynamics through association with BCL2L1 isoform Bcl-X(L) which stimulates its GTPase activity in synaptic vesicles; the function may require its recruitment by MFF to clathrin-containing vesicles. Required for programmed necrosis execution.
Tissue Specificity:	Ubiquitously expressed with highest levels found in skeletal muscles, heart, kidney and brain. Isoform 1 is brain-specific. Isoform 2 and isoform 3 are predominantly expressed in testis and skeletal muscles respectively. Isoform 4 is weakly expressed in brain, heart and kidney. Isoform 5 is dominantly expressed in liver, heart and kidney. Isoform 6 is expressed in neurons.
Involvement in Disease:	Encephalopathy due to defective mitochondrial and peroxisomal fission 1: A rare autosomal dominant systemic disorder resulting in lack of neurologic development and death in infancy. After birth, infants present in the first week of life with poor feeding and neurologic impairment, including hypotonia, little spontaneous movement, no tendon reflexes, no response to light stimulation, and poor visual fixation. Other features include mildly elevated plasma concentration of very-long-chain fatty acids, lactic acidosis, microcephaly, deep-set eyes, optic atrophy and hypoplasia, and an abnormal gyral pattern in both frontal lobes associated with dysmyelination.
Sequence Similarities:	Belongs to the TRAFAC class dynamin-like GTPase superfamily. Dynamin/Fzo/YdjA family.
Post-Translational Modification:	Phosphorylation/dephosphorylation events on two sites near the GED domain regulate mitochondrial fission. Phosphorylation on Ser-637 inhibits the GTPase activity, leading to a defect in mitochondrial fission promoting mitochondrial elongation. Dephosphorylated on this site by PPP3CA which promotes mitochondrial fission. Phosphorylation on Ser-616 activates the GTPase activity and promotes mitochondrial fission.
Cellular Location:	Cytoplasm > Cytosol. Golgi apparatus. Endomembrane system. Mitochondrion outer membrane. Peroxisome. Membrane > Clathrin-coated pit. Cytoplasmic vesicle > Secretory vesicle > Synaptic vesicle membrane. Mainly cytosolic. Translocated to the mitochondrial membrane through O-GlcNAcylation and interaction with FIS1. Recruited to the mitochondrial outer membrane by interaction with MIEF1. Colocalized with MARCH5 at mitochondrial membrane. Localizes to mitochondria at sites of division. Localizes to mitochondria following necrosis induction. Associated with peroxisomal membranes, partly recruited there by PEX11B. May also be associated with endoplasmic reticulum tubules and cytoplasmic vesicles and found to be perinuclear. In some cell types, localizes to the Golgi complex. Binds to phospholipid membranes.
Database Links:	Entrez Gene: 10059?Human Entrez Gene: 74006?Mouse Entrez Gene: 114114?Rat Omim: 603850?Human SwissProt: O00429?Human SwissProt: Q8K1M6?Mouse SwissProt: O35303?Rat Unigene: 556296?Human Unigene: 218820?Mouse Unigene: 216851?Rat
Synonyms:	DLP1 Antibody dnm1l Antibody DNM1L_HUMAN Antibody Dnm1p/Vps1p-like protein Antibody dnml1 Antibody DRP1 Antibody DVLP Antibody Dymple Antibody Dynamin 1 like Antibody Dynamin family member proline-rich carboxyl-terminal domain less Antibody Dynamin like protein Antibody Dynamin related protein 1 Antibody Dynamin-1-like protein Antibody Dynamin-like protein Antibody Dynamin-like protein 4 Antibody Dynamin-like protein IV Antibody Dynamin-related protein 1 Antibody DYNIV 11 Antibody EMPF Antibody EMPF1 Antibody FLJ41912 Antibody HdynIV Antibody VPS1 Antibody
Information:	Target information shown above is from the UniProt Consortium.