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Key Documents

PC253L

Sigma-Aldrich

抗-钙结合蛋白D-28K (Ab-1) 兔pAb

lyophilized, Calbiochem®

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About This Item

分類程式碼代碼:
12352203
NACRES:
NA.43

生物源

rabbit

品質等級

抗體表格

serum

抗體產品種類

primary antibodies

無性繁殖

polyclonal

形狀

lyophilized

包含

≤0.1% sodium azide as preservative

物種活性

baboon, monkey, rat, human

製造商/商標名

Calbiochem®

儲存條件

OK to freeze
avoid repeated freeze/thaw cycles

同型

IgG

運輸包裝

ambient

儲存溫度

−20°C

目標翻譯後修改

unmodified

基因資訊

human ... CALB1(793)
rhesus monkey ... Calb1(677721)

一般說明

兔多克隆抗体以冻干未稀释的血清形式提供。可识别钙结合蛋白D-28K蛋白。
兔多克隆抗钙结合蛋白D-28K(Ab-1)可重新识别大鼠海马中的钙结合蛋白D-28K蛋白。经验证可用于冰冻切片和T细胞共刺激。
可识别大鼠海马组织中的钙结合蛋白D-28K蛋白。

免疫原

纯化牛小脑钙结合蛋白D-28K蛋白

應用

冷冻切片(整个安装/振动切片机切片,1:1000,荧光)

振动切片机切片(生物素-链霉亲和素/过氧化物酶检测为1:5000-1:10,000,请参阅应用参考文献)

警告

毒性:标准处理(A)

外觀

未稀释的血清。

重構

用100 µl无菌蒸馏H₂O复溶冻干抗体。所得复溶溶液将包含≤0.1%叠氮化钠。注意复溶小瓶的全部内容物;在运输和处理过程中,冻干颗粒的部分可能已脱落,可能不在小瓶底部。用无菌PBS或Tris缓冲液稀释,稀释度不高于1:10。溶解后,等分并冷冻保存(-20°C)。储备溶液在-20°C下可稳定保存至多6个月。避免溶液反复冻融。

分析報告

阳性对照
大鼠纹状体、海马或皮质

其他說明

Conde, F., et al. 1994.J. Comp.Neurol.341, 95.
Heizmann, C.W.1993.Acta Neurobiol.Exp.53, 15.
Baimbridge, K.G., et al. 1992.Trends Neurosci.15, 303.
Heizmann, C.W. and Hunziker, W. 1992.Trends Biochem.Sci.16, 98.
在大鼠纹状体,皮层和海马中检查了抗体特异性。根据生产商说明,使用生物素-链霉亲和素/过氧化物酶试剂检测一抗。在单个系统中,应对抗体进行滴定以获得最佳结果。

法律資訊

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

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儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 1

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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Gaucher disease is characterized by lysosomal accumulation of glucosylceramide due to deficient activity of lysosomal glucocerebrosidase (GBA). In cells, glucosylceramide is also degraded outside lysosomes by the enzyme glucosylceramidase 2 (GBA2) of which inherited deficiency is associated with ataxias. The
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The decline in visual function due to normal aging impacts various aspects of our daily lives. Previous reports suggest that the aging retina exhibits mislocalization of photoreceptor terminals and reduced amplitudes of scotopic and photopic electroretinogram (ERG) responses in mice.
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The enzyme glucocerebrosidase (GBA) hydrolyses glucosylceramide (GlcCer) in lysosomes. Markedly reduced GBA activity is associated with severe manifestations of Gaucher disease including neurological involvement. Mutations in the GBA gene have recently also been identified as major genetic risk factor for
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