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Anti-Reelin, clone G10, Alexa Fluor® 488 Conjugate

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号:MAB5364A4

牌:Millipore 密理博

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Replacement Information

重要规格表

Species Reactivity Key Applications Host Format Antibody Type
M, R ICC, IHC M AlexaFluor®488 Monoclonal Antibody
Description
Catalogue Number MAB5364A4
Description Anti-Reelin Antibody, clone G10, Alexa Fluor® 488 Conjugate
Alternate Names
  • Reelin
Background Information Reelin, a glycoprotein, plays a crucial role during embryonic neuronal migration, primarily as a regulator of corticogenesis and neuronal cell positioning in the prenatal period. In adults, reelin may act as a modulator of synaptic plasticity. Reelin has been implicated to play a role in several brain diseases including schizphrenia, Alzheimers's disease, temporal lobe epilespy, and autism. Reelin is found in the brain, spinal cord, blood, and other body organs and tissues.
References
Product Information
Format AlexaFluor®488
Control
  • Adult mouse brain tissue
Presentation Purified mouse monoclonal IgG1 conjugated to Alexa Fluor® 488 in PBS with 0.1% sodium azide and 15 mg/mL BSA.
Applications
Application Anti-Reelin Antibody, clone G10, Alexa Fluor 488 Conjugate detects level of Reelin & has been published & validated for use in IC, IH.
Key Applications
  • Immunocytochemistry
  • Immunohistochemistry
Application Notes Immunocytochemistry Analysis: A 1:400 dilution from a representative lot detected Reelin in rat E18 primary cortex cells.
Biological Information
Immunogen Recombinant protein corresponding to rat Reelin.
Clone G10
Host Mouse
Isotype IgG
Species Reactivity
  • Mouse
  • Rat
Antibody Type Monoclonal Antibody
Entrez Gene Number
Entrez Gene Summary 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.
Gene Symbol
  • Reln
Purification Method Protein A Purfied
UniProt Number
UniProt Summary FUNCTION: 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: The basic C-terminal region is essential for secretion (By similarity).

DISEASE: 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.
Molecular Weight 388 kDa calculated
Physicochemical Information
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
Safety Information
Product Usage Statements
Quality Assurance Evaluated by Immunohistochemistry in adult mouse brain tissue.

Immunohistochemistry Analysis: A 1:100 dilution of this antibody detected Reelin in adult mouse brain tissue.
Usage Statement
  • 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.
Storage and Shipping Information
Storage Conditions Maintain refrigerated at 2-8 °C protected from light in undiluted aliquots for up to 6 months from date of receipt.
Packaging Information
Material Size 100 µL
Transport Information
Supplemental Information
Specifications

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