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MAB1581

Sigma-Aldrich

Anti-Chondroitin Sulfate Proteoglycan Antibody, Core Protein Epitope, clone Cat-315

ascites fluid, clone Cat-315, Chemicon®

Synonyme(s) :

CSPG

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About This Item

Code UNSPSC :
12352203
eCl@ss :
32160702
Nomenclature NACRES :
NA.41

Source biologique

mouse

Niveau de qualité

100

Forme d'anticorps

ascites fluid

Type de produit anticorps

primary antibodies

Clone

Cat-315, monoclonal

Espèces réactives

feline, rat

Fabricant/nom de marque

Chemicon®

Technique(s)

immunocytochemistry: suitable
immunohistochemistry: suitable
immunoprecipitation (IP): suitable
western blot: suitable

Isotype

IgM

Numéro d'accès UniProt

P16112

Conditions d'expédition

dry ice

Modification post-traductionnelle de la cible

unmodified

Informations sur le gène

human ... ACAN(176)

Spécificité

Chondroitin sulfate proteoglycan (CSPG), protein core epitope

Immunogène

Epitope: Core Protein Epitope

Application

Immunohistochemistry: 1:2,000 on 4% paraformaldehyde fixed frozen tissue.

Immunocytochemistry: 1:500 on primary cultures of neurons.

Immunoblot: 1:5,000 recognizes a band at 680 kDa.

Immunoprecipitation.

Optimal working dilutions must be determined by the end user.
This Anti-Chondroitin Sulfate Proteoglycan Antibody, Core Protein Epitope, clone Cat-315 is validated for use in IP, WB, IC, IH for the detection of Chondroitin Sulfate Proteoglycan.

Informations légales

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

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Code de la classe de stockage

12 - Non Combustible Liquids

Classe de danger pour l'eau (WGK)

nwg

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

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Claudia Loebel et al.
Advanced functional materials, 30(44) (2021-07-03)
Hydrogels are engineered with biochemical and biophysical signals to recreate aspects of the native microenvironment and to control cellular functions such as differentiation and matrix deposition. This deposited matrix accumulates within the pericellular space and likely affects the interactions between
Paulette A McRae et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 27(20), 5405-5413 (2007-05-18)
An important role for the neural extracellular matrix in modulating cortical activity-dependent synaptic plasticity has been established by a number of recent studies. However, identification of the critical molecular components of the neural matrix that mediate these processes is far
Andrew Nathaniel Stewart et al.
Restorative neurology and neuroscience, 35(4), 395-411 (2017-06-10)
Utilizing genetic overexpression of trophic molecules in cell populations has been a promising strategy to develop cell replacement therapies for spinal cord injury (SCI). Over-expressing the chemokine, stromal derived factor-1 (SDF-1α), which has chemotactic effects on many cells of the
Alicia L Hawthorne et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 30(2), 420-430 (2010-01-15)
Embryonic CNS neurons can migrate from the ventricular zone to their final destination by radial glial-guided locomotion. Another less appreciated mechanism is somal translocation, where the young neuron maintains its primitive ventricular and pial processes, through which the cell body
Eleanor Grant et al.
Cerebral cortex (New York, N.Y. : 1991), 26(3), 1336-1348 (2016-01-09)
Corticothalamic projection systems arise from 2 main cortical layers. Layer V neurons project exclusively to higher-order thalamic nuclei, while layer VIa fibers project to both first-order and higher-order thalamic nuclei. During early postnatal development, layer VIa and VIb fibers accumulate
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