Anti-DRP1 Antibody (CAB2586)
- SKU:
- CAB2586
- Product type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Reactivity:
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Research Area:
- Cell Biology
Frequently bought together:
Description
| 抗体名: | Anti-DRP1 Antibody |
| 抗体コード: | CAB2586 |
| 抗体サイズ: | 20uL, 50uL, 100uL |
| 申し込み: | WB IF |
| 反応性: | Human, Mouse, Rat |
| 宿主種: | Rabbit |
| 免疫原: | Recombinant fusion protein containing a sequence corresponding to amino acids 411-710 of human DRP1 (NP_036193.2). |
| 申し込み: | WB IF |
| 推奨希釈: | WB 1:500 - 1:2000 IF 1:50 - 1:200 |
| 反応性: | Human, Mouse, Rat |
| ポジティブサンプル: | Mouse brain, Rat brain |
| 免疫原: | Recombinant fusion protein containing a sequence corresponding to amino acids 411-710 of human DRP1 (NP_036193.2). |
| 精製方法: | Affinity purification |
| ストレージバッファ: | Store at -20'C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
| アイソタイプ: | IgG |
| 順序: | VSFE LLVK RQIK RLEE PSLR CVEL VHEE MQRI IQHC SNYS TQEL LRFP KLHD AIVE VVTC LLRK RLPV TNEM VHNL VAIE LAYI NTKH PDFA DACG LMNN NIEE QRRN RLAR ELPS AVSR DKLI QDSR RETK NVAS GGGG VGDG VQEP TTGN WRGM LKTS KAEE LLAE EKSK PIPI MPAS PQKG HAVN LLDV PVPV ARKL SARE QRDC EVIE RLIK SYFL IVRK NIQD SVPK AVMH FLVN HVKD TLQS ELVG QLYK SSLL DDLL TESE DMAQ RRKE AADM LKAL QGAS QIIA EIRE THLW |
| 遺伝子ID: | 10059 |
| Uniprot: | O00429 |
| セルラーロケーション: | Cytoplasm, Cytoplasmic vesicle, Endomembrane system, Golgi apparatus, Membrane, Mitochondrion outer membrane, Peripheral membrane protein, Peroxisome, clathrin-coated pit, cytosol, secretory vesicle, synaptic vesicle membrane |
| 計算された分子量: | 60kDa/78kDa/79kDa/80kDa/81kDa/82kDa/83kDa |
| 観察された分子量: | 78KDa |
| 同義語: | DNM1L, DLP1, DRP1, DVLP, DYMPLE, EMPF, EMPF1, HDYNIV |
| バックグラウンド: | 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. |
| UniProt Protein Function: | DRP1: Functions in mitochondrial and peroxisomal division. Mediates membrane fission through oligomerization into ring-like structures which wrap around the scission site to constict and sever the mitochondrial membrane through a GTP hydrolysis- dependent mechanism. Required for normal brain development. Facilitates developmentally-regulated apoptosis during neural tube development. Required for a normal rate of cytochrome c release and caspase activation during apoptosis. Also required for mitochondrial fission during mitosis. May be involved in vesicle transport. Homotetramer; dimerizes through the N-terminal GTP-middle region of one molecule binding to the GED domain of another DNM1L molecule. Can self-assemble in multimeric ring-like structures. Interacts with BCL2L1; the interaction stimulates the GTPase activity of DMN1L in synapses and increases the number of axonal mitochondria and the size and number of synaptic vesicle clusters. Interacts with FIS1. Interacts with GSK3B and MARCH5. Interacts (via the GTPase and B domains) with UBE2I; the interaction promotes sumoylation of DNM1L, mainly in ite B domain. Interacts with PPP3CA; the interaction dephosphorylates DNM1L and regulates its transition to mitochondria. Interacts witn MID49 and MID51. 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. Belongs to the dynamin family. 6 isoforms of the human protein are produced by alternative splicing. |
| UniProt Protein Details: | Protein type:Endoplasmic reticulum; Mitochondrial; Microtubule-binding; EC 3.6.5.5; Apoptosis; Hydrolase; Motor Chromosomal Location of Human Ortholog: 12p11.21 Cellular Component: Golgi apparatus; microtubule; protein complex; intracellular membrane-bound organelle; synaptic vesicle membrane; mitochondrion; coated pit; cytosol; mitochondrial outer membrane; membrane; perinuclear region of cytoplasm; cytoplasm; peroxisome; cell junction Molecular Function:GTPase activity; identical protein binding; protein binding; protein homodimerization activity; GTP binding; ubiquitin protein ligase binding; lipid binding Biological Process: peroxisome fission; mitochondrial fission; release of cytochrome c from mitochondria; positive regulation of protein secretion; positive regulation of apoptosis; apoptosis; metabolic process; regulation of protein oligomerization; endocytosis; mitochondrial fragmentation during apoptosis; cell structure disassembly during apoptosis; protein homotetramerization Disease: Encephalopathy, Lethal, Due To Defective Mitochondrial And Peroxisomal Fission |
| NCBI Summary: | 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] |
| UniProt Code: | O00429 |
| NCBI GenInfo Identifier: | 125987821 |
| NCBI Gene ID: | 10059 |
| NCBI Accession: | O00429.2 |
| UniProt Secondary Accession: | O00429,O14541, O60709, Q59GN9, Q7L6B3, Q8TBT7, Q9BWM1 Q9Y5J2, A8K4X9, B4DGC9, B4DSU8, J3KPI2, |
| UniProt Related Accession: | O00429 |
| Molecular Weight: | 736 |
| NCBI Full Name: | Dynamin-1-like protein |
| NCBI Synonym Full Names: | dynamin 1-like |
| NCBI Official Symbol: | DNM1L |
| NCBI Official Synonym Symbols: | DLP1; DRP1; DVLP; EMPF; DYMPLE; HDYNIV |
| NCBI Protein Information: | dynamin-1-like protein; dynamin-like protein 4; dynamin-like protein IV; Dnm1p/Vps1p-like protein; dynamin-related protein 1; dynamin family member proline-rich carboxyl-terminal domain less |
| UniProt Protein Name: | Dynamin-1-like protein |
| UniProt Synonym Protein Names: | 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 |
| Protein Family: | Dynamin-1-like protein |
| UniProt Gene Name: | DNM1L |
| UniProt Entry Name: | DNM1L_HUMAN |
 | Western blot analysis of extracts of various cell lines, using DRP1 Rabbit pAb (CAB2586) at 1:8000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) (CABS014) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit (RM00020). Exposure time: 1s. |
 | Immunofluorescence analysis of HeLa cells using DRP1 antibody (CAB2586). Blue: DAPI for nuclear staining. |
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