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Merck
CN

MAB5284

Anti-Aggrecan Antibody

CHEMICON®, mouse monoclonal, Cat-301

别名:

CSPG

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关于此项目

UNSPSC Code:
12352203
eCl@ss:
32160702
NACRES:
NA.41
Clone:
Cat-301, monoclonal
Species reactivity:
primate, human, rat, gerbil, feline, hamster, guinea pig
Application:
immunocytochemistry
immunohistochemistry
immunoprecipitation (IP)
western blot
Technique(s):
immunocytochemistry: suitable
immunohistochemistry: suitable
immunoprecipitation (IP): suitable
western blot: suitable
Citations:
36
Uniprot accession no.:
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产品名称

硫酸软骨素蛋白聚糖抗体,脑(核心蛋白),克隆Cat-301, clone Cat-301, Chemicon®, from mouse

biological source

mouse

antibody form

purified immunoglobulin

antibody product type

primary antibodies

clone

Cat-301, monoclonal

species reactivity

primate, human, rat, gerbil, feline, hamster, guinea pig

manufacturer/tradename

Chemicon®

technique(s)

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

isotype

IgG1

NCBI accession no.

UniProt accession no.

shipped in

wet ice

target post-translational modification

unmodified

Quality Level

Gene Information

human ... ACAN(176)

Application

免疫组化:4%多聚甲醛固定的冷冻组织上按1:500-1:2,000。

免疫组化

免疫印迹

免疫沉淀

最佳工作稀释度必须由最终用户确定。
硫酸软骨素蛋白聚糖抗体(脑(核心蛋白),克隆Cat-301)可检测硫酸软骨素蛋白聚糖水平& 已发表 & 经验证可用于IP,、WB、IC、IH。

Biochem/physiol Actions

硫酸软骨素蛋白聚糖(CSPG),脑核心蛋白。

General description

克隆CAT-301识别的抗原是一种受发育调控的蛋白聚糖,是存在于哺乳动物神经元细胞外表面的高分子硫酸软骨素蛋白聚糖。它在发育后期表达,尽管尚未确定CAT-301的确切作用,但据信它在突触结构的稳定中起作用。

该名称来源于最初用于通过其表达进行鉴定的单克隆抗体的名称,该抗体通过免疫细胞化学进行检测



在关键的出生早期,通过物理或生化手段破坏神经元活动的正常模式会导致CAT-301水平大幅度不可逆地降低。对成熟动物的类似干预没有作用。



CAT-301与关节软骨中的聚集蛋白聚糖有关。CAT-301抗体可与聚集蛋白聚糖发生免疫反应,软骨素酶处理的聚集蛋白聚糖和CAT-301的表观分子量均为550kDa。但是,CAT-301不会像聚集蛋白聚糖那样被硫酸角质素糖基化。

Immunogen

猫脊髓固定灰质。
表位:脑(核心蛋白)

Other Notes

浓度:请参考批次特异性浓缩物的检验报告。

Physical form

形式:纯化

Legal Information

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

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存储类别

10 - Combustible liquids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable


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Lena Iwai et al.
Cerebral cortex (New York, N.Y. : 1991), 23(9), 2204-2212 (2012-07-14)
Although the parallel visual pathways are a fundamental basis of visual processing, our knowledge of their molecular properties is still limited. Here, we uncovered a parvocellular-specific molecule in the dorsal lateral geniculate nucleus (dLGN) of higher mammals. We found that
Otavio S C Mariani et al.
The Journal of comparative neurology, 527(3), 694-717 (2018-03-27)
We propose a partitioning of the primate intraparietal sulcus (IPS) using immunoarchitectural and connectivity criteria. We studied the immunoarchitecture of the IPS areas in the capuchin monkey using Cat-301 and SMI-32 immunohistochemistry. In addition, we investigated the IPS projections to
Vasily Vorobyov et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 33(1), 234-243 (2013-01-04)
Monocular deprivation (MD) during a critical period of postnatal development produces significant changes in the anatomy and physiology of the visual cortex, and the deprived eye becomes amblyopic. Extracellular matrix molecules have a major role in restricting plasticity such that
Daniel L Felch et al.
Frontiers in neuroanatomy, 6, 12-12 (2012-04-20)
Previous research has suggested that the three physiologically defined relay cell-types in mammalian lateral geniculate nucleus (LGN)-called parvocellular (P), magnocellular (M), and koniocellular (K) cells in primates and X, Y, and W cells in other mammals-each express a unique combination
Danai Riga et al.
Science translational medicine, 9(421) (2017-12-22)
Patients with depression often suffer from cognitive impairments that contribute to disease burden. We used social defeat-induced persistent stress (SDPS) to induce a depressive-like state in rats and then studied long-lasting memory deficits in the absence of acute stressors in

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