Anti-GFAP Polyclonal Antibody-抗体-抗体-生物在线

Anti-GFAP Polyclonal Antibody

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产品名称： Anti-GFAP Polyclonal Antibody

英文名称： Anti-GFAP Polyclonal Antibody

产品编号： K001616P

产品价格： null

产品产地：北京

品牌商标： Solarbio

更新时间： 2025-11-06T11:14:17

使用范围：

北京索莱宝科技有限公司

联系人 : 索莱宝-龚思雨
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产品详情

Anti-GFAP Polyclonal Antibody
品牌：Solarbio | 货号：K001616P
K001616P-50ul Solarbio 50ul 960.00元 
K001616P-100ul Solarbio 100ul 1600.00元
英文名称 Rabbit GFAP Polyclonal Antibody
应用2 WB IHC IF
克隆类型2 Polyclonal Antibody
别名 ALXDRD 
应用 WB,IHC,IF
稀释比例 WB1:500-1:2000 IHC1:50-1:200 IF1:50-1:100
交叉反应 Human Mouse Rat
蛋白分子量 50kDa
Gene ID 2670
保存 Store at -20°C. Avoid freeze / thaw cycles.Stable for one year from the date of shipment.
储存液 PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
纯化方法 Affinity purification
亚型 IgG
免疫原 A synthetic peptide of human GFAP
性状 Lyophilized or Liquid
Swiss Prot P14136
克隆类型 Polyclonal Antibody
来源 Rabbit
背景资料 This gene encodes one of the major intermediate filament proteins of mature astrocytes. It is used as a marker to distinguish astrocytes from other glial cells during development. Mutations in this gene cause Alexander disease, a rare disorder of astrocytes in the central nervous system. Alternative splicing results in multiple transcript variants encoding distinct isoforms.

K001616P-50ul	Solarbio	50ul	960.00元
K001616P-100ul	Solarbio	100ul	1600.00元

英文名称	Rabbit GFAP Polyclonal Antibody
应用2	WB IHC IF
克隆类型2	Polyclonal Antibody
别名	ALXDRD
应用	WB,IHC,IF
稀释比例	WB1:500-1:2000 IHC1:50-1:200 IF1:50-1:100
交叉反应	Human Mouse Rat
蛋白分子量	50kDa
Gene ID	2670
保存	Store at -20°C. Avoid freeze / thaw cycles.Stable for one year from the date of shipment.
储存液	PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
纯化方法	Affinity purification
亚型	IgG
免疫原	A synthetic peptide of human GFAP
性状	Lyophilized or Liquid
Swiss Prot	P14136
克隆类型	Polyclonal Antibody
来源	Rabbit
背景资料	This gene encodes one of the major intermediate filament proteins of mature astrocytes. It is used as a marker to distinguish astrocytes from other glial cells during development. Mutations in this gene cause Alexander disease, a rare disorder of astrocytes in the central nervous system. Alternative splicing results in multiple transcript variants encoding distinct isoforms.