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MAB5366

Sigma-Aldrich

Anti-Reelin Antibody, a.a. 164-189 mreelin, clone 142

clone 142, Chemicon®, from mouse

Synonim(y):

reelin

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About This Item

Kod UNSPSC:
12352203
eCl@ss:
32160702
NACRES:
NA.41

pochodzenie biologiczne

mouse

Poziom jakości

forma przeciwciała

purified antibody

rodzaj przeciwciała

primary antibodies

klon

142, monoclonal

reaktywność gatunkowa

mouse, vertebrates, human

reaktywność gatunkowa (przewidywana na podstawie homologii)

rat

producent / nazwa handlowa

Chemicon®

metody

immunohistochemistry: suitable
western blot: suitable

izotyp

IgG1

numer dostępu NCBI

numer dostępu UniProt

Warunki transportu

wet ice

docelowa modyfikacja potranslacyjna

unmodified

informacje o genach

human ... RELN(5649)

Opis ogólny

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.

Specyficzność

Reelin. The epitope is between amino acids 164 and 189.

Immunogen

Epitope: a.a. 164-189
Recombinant reelin amino acids 40-189.

Zastosowanie

Research Category
Neuroscience
Research Sub Category
Growth Cones & Axon Guidance
This Anti-Reelin Antibody, a.a. 164-189 mreelin, clone 142 is validated for use in IH, WB for the detection of Reelin.
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.

Jakość

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.

Opis wartości docelowych

In Western blots, reelin can appear as three bands ~400 - 450, 300, and 180 - 200 kDa′s.

Postać fizyczna

Format: Purified
Protein A purified
Purified mouse monoclonal IgG1 in buffer containing 0.02M Phosphate buffer with 0.25M NaCl and 0.1% sodium azide.

Przechowywanie i stabilność

Stable for 6 months at 2-8ºC in undiluted aliquots from date of receipt.

Komentarz do analizy

Control
Mouse liver or kidney

Inne uwagi

Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.

Informacje prawne

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany

Oświadczenie o zrzeczeniu się odpowiedzialności

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.
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Kod klasy składowania

10 - Combustible liquids

Klasa zagrożenia wodnego (WGK)

WGK 2

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable


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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Changes in cell migration and survival in the olfactory bulb of the pcd/pcd mouse.
J Valero, E Weruaga, A R Murias, J S Recio, G G Curto, C Gomez, J R Alonso
Developmental neurobiology null
K Tsamis et al.
The International journal of neuroscience, 117(1), 25-46 (2007-03-17)
Reelin is a secreted glycoprotein with a crucial role in development of the Central Nervous System. In adults, its function remains unclear but it may be involved in the modulation of synaptic plasticity. Having in mind this possible property of
Brian R Mullen et al.
ASN neuro, 5(1), e00106-e00106 (2013-01-10)
Genetic and environmental factors are both likely to contribute to neurodevelopmental disorders, including ASDs (autism spectrum disorders). In this study, we examined the combinatorial effect of two factors thought to be involved in autism--reduction in the expression of the extracellular
Polymicrogyria includes fusion of the molecular layer and decreased neuronal populations but normal cortical laminar organization.
Judkins, AR; Martinez, D; Ferreira, P; Dobyns, WB; Golden, JA
Journal of Neuropathology and Experimental Neurology null
Transcriptomal comparison of human dermal lymphatic endothelial cells ex vivo and in vitro.
Wick, N; Saharinen, P; Saharinen, J; Gurnhofer, E; Steiner, CW; Raab, I; Stokic et al.
Physiological Genomics null

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