- 当前位置：首页 > >Merck Millipore > 生命科学研究
- 生命科学研究
-
-
merck millipore,默克密理博,MAB5366,Anti-Reelin Antibody, a.a. 164-189 mreelin, clone 142
产品名称：Anti-Reelin Antibody, a.a. 164-189 mreelin, clone 142
产品型号：MAB5366
This Anti-Reelin Antibody, a.a. 164-189 mreelin, clone 142 is validated for use in IH, WB for the detection of Reelin.
merck millipore,默克密理博,MAB5366,Anti-Reelin Antibody, a.a. 164-189 mreelin, clone 142
- 产品介绍
重要规格表
品种反应性 主要应用 宿主 格式 抗体类型 Vrt, H, M WB, IHC M Purified Monoclonal Antibody 描述 产品目录编号 MAB5366 品牌系列 Chemicon®
商名 - Chemicon
描述 Anti-Reelin Antibody, a.a. 164-189 mreelin, clone 142 Alternate Names - reelin
背景信息 The highly layered structure of the cerebral cortex is established through the pattern of neuronal cell migrations. The first step is the creation of the primordial layer, the preplate, consisting of radial glial cells and the earliest generated neurons. Among these neurons are the Cajal-Retzius neurons. In the next step, the preplate splits into a superficial (marginal) zone, where the Cajal-Retzius neurons reside, and a deep subplate wherein the neurons form. Neurons migrating from the subplate form the cortical plate. This migration takes place on the radial glial fibers.
The reeler mutant in mouse displays an abnormal pattern of cell migration throughout the cerebral and cerebellar cortices. The preplate forms normally, and the neurons differentiate at the correct times in the ventricular zone. However, instead of forming the normal "inside-out" arrangement of neurons in the cortical plate, the older neurons are found furthest from the ventricular zone, while the younger neurons do not migrate far at all. The reeler cerebral cortex is inverted from that of the wild type mouse.
The defect of the reeler mice appears to be in the production of an extracellular matrix protein by the Cajal-Retzius cells (D'Arcangelo et al., 1995, Nature 374:719-723.; Ogawa et al., 1995 Neuron 14:899-912.) This 388kDa protein is made by wild-type mice but not by the reeler mutants. It is thought that this Reelin protein is crucial for positioning the migrating neuron within the cortical plate (Figure 1). In the absence of Reelin, the migrating neuron would be "lost," and the cortical plate would be abnormal. We do not yet know the mechanisms by which Reelin informs the cells as to their position, how the cell responds to Reelin, and why the absence of reelin should give an "inverted" plate. However, the identification of the protein encoded by the reeler gene should allow us to begin these studies.产品信息 格式 Purified 控制 - Mouse liver or kidney
演示 Purified mouse monoclonal IgG1 in buffer containing 0.02M Phosphate buffer with 0.25M NaCl and 0.1% sodium azide. 应用 应用 This Anti-Reelin Antibody, a.a. 164-189 mreelin, clone 142 is validated for use in IH, WB for the detection of Reelin. 主要应用 - Western Blotting
- Immunohistochemistry
应用说明 Western blot:
1:250-1:500, In Western blots, reelin appears as three bands ~400 - 450, 300, and 180 - 200 kDa's.
Immunohistochemistry:
1:250-1:500, 4% PFA fixed tissues. A previous lot of this antibody was used in IH.
Optimal working dilutions must be determined by the end user.生物信息 免疫原品种 Recombinant reelin amino acids 40-189. 表位 a.a. 164-189 克隆 142 浓缩 Please refer to the Certificate of Analysis for the lot-specific concentration. 宿主 Mouse 特异性 Reelin. The epitope is between amino acids 164 and 189. 同种型 IgG1 品种反应性 VertebratesHumanMouse Species Reactivity Note Expected to react with rat based on sequence homology. 抗体类型 Monoclonal Antibody Entrez基因编号 - NM_005045.2
Entrez基因汇总 This gene encodes a large secreted extracellular matrix protein thought to control cell-cell interactions critical for cell positioning and neuronal migration during brain development. This protein may be involved in schizophrenia, autism, bipolar disorder, major depression and in migration defects associated with temporal lobe epilepsy. Mutations of this gene are associated with autosomal recessive lissencephaly with cerebellar hypoplasia. Two transcript variants encoding distinct isoforms have been identified for this gene. Other transcript variants have been described but their full length nature has not been determined. 基因符号 - EC 3.4.21.-
- RELN
- RL
纯化方法 Protein A purfied UniProt编号 - P78509
UniProt汇总 FUNCTION: SwissProt: P78509 # Extracellular matrix serine protease that plays a role in layering of neurons in the cerebral cortex and cerebellum. Regulates microtubule function in neurons and neuronal migration. Affects migration of sympathetic preganglionic neurons in the spinal cord, where it seems to act as a barrier to neuronal migration. Enzymatic activity is important for the modulation of cell adhesion. Binding to the extracellular domains of lipoprotein receptors VLDLR and ApoER2 induces tyrosine phosphorylation of Dab1 and modulation of Tau phosphorylation (By similarity).
SIZE: 3460 amino acids; 388402 Da
SUBUNIT: Binds to the ectodomains of VLDLR and ApoER2 (By similarity).
SUBCELLULAR LOCATION: Secreted (By similarity).
TISSUE SPECIFICITY: Abundantly produced during brain ontogenesis by the Cajal-Retzius cells and other pioneer neurons located in the telencephalic marginal zone and by granule cells of the external granular layer of the cerebellum. In adult brain, preferentially expressed in GABAergic interneurons of prefrontal cortices, temporal cortex, hippocampus and glutamatergic granule cells of cerebellum. Also expressed in fetal and adult liver.
DEVELOPMENTAL STAGE: Expressed in fetal and postnatal brain and liver. Expression in postnatal human brain is high in the cerebellum.
DOMAIN: SwissProt: P78509 The basic C-terminal region is essential for secretion (By similarity).
DISEASE: SwissProt: P78509 # Defects in RELN are the cause of autosomal recessive lissencephaly with cerebellar hypoplasia [MIM:257320]; also known as Norman-Roberts syndrome. Some patients also displayed persistent lymphedema neonatally, and one showed accumulation of chlyous or fatty, ascites fluid. & Defects in RELN may contribute to susceptibility to schizophrenia. Expression of the protein is reduced to about 50% in patients with schizophrenia. & Defects in RELN may predispose to autistic disorder. A polymorphic GGC triplet repeat located in the 5'-UTR region of RELN gene, which harbors in the normal population 8 to 10 repeats, is significantly increased in autistic patients to carry 4 to 23 additional repeats.
SIMILARITY: Belongs to the reelin family. & Contains 15 BNR repeats. & Contains 8 EGF-like domains. & Contains 1 reelin domain.产品使用声明 质量保证 Routinely evaluated by Western Blot on mouse brain lysates.
Western Blot Analysis:
1:1000 dilution of this lot detected Reelin on 10 μg of mouse brain lysates.使用声明 - Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
储存和货运信息 存储条件 Stable for 6 months at 2-8ºC in undiluted aliquots from date of receipt. 包装信息 数量 100 µg
上一件merck millipore产品：merck millipore,默克密理博,MAMP09608,MultiScreen 多通道打孔器
下一件merck millipore产品：merck millipore,默克密理博,CBL402-K,Anti-Papillomavirus 16 Late 1 Protein, Clone Camvir-1
相关产品
merck millipore,默克密理博,MABC775,Anti-PLAU, clone EPR6273, Rabbit Monoclonal Antibody
merck millipore,默克密理博,SCR038,Human Adipose Mesenchymal Stem Cell Kit
merck millipore,默克密理博,69232,S•Tag™ Thrombin Purification Kit
merck millipore,默克密理博,05-1354,Anti-Histone H3 Antibody (Dimethyl K9, Phospho S10), clone 6HH3-2C5
merck millipore,默克密理博,MAMP09608,MultiScreen 多通道打孔器
merck millipore,默克密理博,CBL402-K,Anti-Papillomavirus 16 Late 1 Protein, Clone Camvir-1
merck millipore,默克密理博,CBL180P,Anti-E-Selectin Antibody, clone 1.2B6, Phycoerythrin conjugated
merck millipore,默克密理博,121765,AG 825 - CAS 149092-50-2 - Calbiochem
merck millipore,默克密理博,20-210,Catch and Release Wash Buffer, 10X