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UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
Clone:
Cat-316, monoclonal
Species reactivity:
feline, rat
Application:
immunocytochemistry
immunohistochemistry
immunoprecipitation (IP)
western blot
immunohistochemistry
immunoprecipitation (IP)
western blot
Technique(s):
immunocytochemistry: suitable
immunohistochemistry: suitable
immunoprecipitation (IP): suitable
western blot: suitable
immunohistochemistry: suitable
immunoprecipitation (IP): suitable
western blot: suitable
Citations:
6
产品名称
Anti-Chondroitin Sulfate Proteoglycan Antibody, carbohydrate epitope, clone Cat-316, ascites fluid, clone Cat-316, Chemicon®
biological source
mouse
antibody form
ascites fluid
antibody product type
primary antibodies
clone
Cat-316, monoclonal
species reactivity
feline, rat
manufacturer/tradename
Chemicon®
technique(s)
immunocytochemistry: suitable
immunohistochemistry: suitable
immunoprecipitation (IP): suitable
western blot: suitable
isotype
IgM
shipped in
dry ice
target post-translational modification
unmodified
Quality Level
Gene Information
rat ... Cspg4(81651)
Application
Anti-Chondroitin Sulfate Proteoglycan Antibody, carbohydrate epitope, clone Cat-316 is an antibody against Chondroitin Sulfate Proteoglycan for use in IP, WB, IC, IH.
Immunohistochemistry: 1:70,000 on 4% paraformaldehyde fixed frozen tissue.
Immunocytochemistry: 1:2,500 on primary cultures of neurons.
Immunoblot: 1:200,000
Immunoprecipitation
Optimal working dilutions must be determined by the end user.
Immunocytochemistry: 1:2,500 on primary cultures of neurons.
Immunoblot: 1:200,000
Immunoprecipitation
Optimal working dilutions must be determined by the end user.
Research Category
Cell Structure
Cell Structure
Research Sub Category
Integrins
Integrins
Biochem/physiol Actions
Chondroitin sulfate proteoglycan (CSPG), carbohydrate epitope
Disclaimer
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.
Immunogen
Epitope: carbohydrate epitope
Feline brain proteoglycans
Physical form
Liquid with 0.1% sodium azide.
Preparation Note
Maintain at -20°C in undiluted aliquots for up to 6 months. Avoid repeated freeze/thaw cycles
Legal Information
CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany
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存储类别
12 - Non Combustible Liquids
wgk
nwg
flash_point_f
Not applicable
flash_point_c
Not applicable
Satomi Nadanaka et al.
Biomolecules, 10(11) (2020-11-05)
The chondroitin sulfate (CS)-rich dense extracellular matrix surrounding neuron cell bodies and proximal dendrites in a mesh-like structure is called a perineuronal net (PNN). CS chains in PNNs control neuronal plasticity by binding to PNN effectors, semaphorin-3A (Sema3A) and orthodenticle
De-Lai Zhao et al.
Molecular medicine reports, 22(4), 2637-2644 (2020-09-19)
Chondrocytes in injured cartilage tissue are susceptible to mechanical loading; mechanical overloading can induce cartilage degeneration. The aim of the present study was to investigate whether mechanical loading can regulate chondrocyte degeneration and angiogenesis via the tissue inhibitor of matrix
Shinji Miyata et al.
Frontiers in integrative neuroscience, 12, 3-3 (2018-02-20)
Aggrecan, a chondroitin sulfate (CS) proteoglycan, forms lattice-like extracellular matrix structures called perineuronal nets (PNNs). Neocortical PNNs primarily ensheath parvalbumin-expressing inhibitory neurons (parvalbumin, PV cells) late in brain development. Emerging evidence indicates that PNNs promote the maturation of PV cells
Hiroshi Ueno et al.
IBRO reports, 4, 22-37 (2018-08-24)
Specific regions of the cerebral cortex are highly plastic in an organism's lifetime. It is thought that perineuronal nets (PNNs) regulate plasticity, but labeling for Wisteria floribunda agglutinin (WFA), which is widely used to detect PNNs, is observed throughout the
Guixin Zhang et al.
The Journal of comparative neurology, 522(9), 2209-2229 (2013-12-21)
Disability following spinal cord injury is due to failure of axon regeneration, which has been ascribed to environmental factors in the central nervous system and a developmental loss of intrinsic growth capacity in neurons. Recently, the receptor-like protein tyrosine phosphatases
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