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膠質纖維酸性蛋白抗體

膠質纖維酸性蛋白抗體
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  • 產品名稱:膠質纖維酸性蛋白抗體
  • 產品型號:
  • 產品展商:單克隆抗體/多克隆抗體
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簡單介紹
膠質纖維酸性蛋白抗體應用于IHC、WB、 IF、IP、ELISA等科研實驗,按理化性質和生物學功能IgM、IgG、IgA、IgE、IgD五類。按抗體的來源,可將其分為天然抗體和**抗體。膠質纖維酸性蛋白抗體生產每個流程都執(zhí)行嚴格的檢測標準,保證蛋白抗原產品質量,質量穩(wěn)定,實驗效果明顯。
產品描述

膠質纖維酸性蛋白抗體


規(guī)格:1mg/1ml

英文名: GFAP

別名: Astrocyte; FLJ45472; GFAP; Glial Fibrillary Acidic Protein; Intermediate filament protein; GFAP_HUMAN.

分子量: 48kDa

儲存液:0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glyce

克隆類型:Polyclonal

亞型:IgG

純化方法:affinity purified by Protein A

**原:KLH conjugated synthetic peptide derived from human GFAP

交叉反應:Human, Mouse, Rat, Dog, Pig, Cow, Rabbit, Sheep,

膠質纖維酸性蛋白抗體細胞定位:細胞漿

產品介紹:background: 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. [provided by RefSeq, Oct 2008] Function: GFAP, a class-III intermediate filament, is a cell-specific marker that, during the development of the central nervous system, distinguishes astrocytes from other glial cells. Subunit: Interacts with SYNM. Isoform 3 interacts with PSEN1 (via N-terminus). Subcellular Location: Cytoplasm. Note=Associated with intermediate filaments. Tissue Specificity: Expressed in cells lacking fibronectin. Post-translational modifications: Phosphorylated by PKN1. DISEASE: Defects in GFAP are a cause of Alexander disease (ALEXD) [MIM:203450]. Alexander disease is a rare disorder of the central nervous system.膠質纖維酸性蛋白抗體 It is a progressive leukoencephalopathy whose hallmark is the widespread accumulation of Rosenthal fibers which are cytoplasmic inclusions in astrocytes. The most common form affects infants and young children, and is characterized by progressive failure of central myelination, usually leading to death usually within the first decade. Infants with Alexander disease develop a leukoencephalopathy with macrocephaly, seizures, and psychomotor retardation. Patients with juvenile or ***** forms typically experience ataxia, bulbar signs and spasticity, and a more slowly progressive course. Similarity: Belongs to the intermediate filament family. Gene ID: 2670 Database links: Entrez Gene: 281189 Cow Entrez Gene: 2670 Human Entrez Gene:膠質纖維酸性蛋白抗體 14580 Mouse Entrez Gene: 24387 Rat Omim: 137780 Human SwissProt: Q28115 Cow SwissProt: P14136 Human SwissProt: P03995 Mouse Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. 星形膠質細胞標志物 (Astrocyte Marker) GFAP是一個56kDa的中間絲蛋白(intermediate filament,IF),在**神經系統發(fā)育期是一個特異性的標志物,以區(qū)別星形細胞和其它膠質細胞。GFAP表達在皮層和海馬,急、慢性皮質酮**時表達減少。 GFAP可以和人、大鼠、小鼠的GFAP反應,在正常和腫瘤性的星形膠質細胞陽性表達,而神經節(jié)細胞、神經元、成纖維細胞、少突膠質細胞和這些細胞來源的腫瘤細胞陰性表達,主要用于星形膠質瘤等**神經系統腫瘤的診斷和鑒別診斷,GFAP的缺乏可導致AD病。

膠質纖維酸性蛋白抗體產品應用:WB=1:100-500 ELISA=1:500-1000 IHC-P=1:200-1000 IHC-F=1:200-1000 Flow-Cyt=1:50-500 ICC=1:200-1000 IF=1:200-1000 (石蠟切片需做抗原修復) not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.

研究領域:腫瘤  細胞生物  **學  神經生物學  信號轉導  干細胞  細胞粘附分子  細胞類型標志物  細胞骨架  

儲存條件: Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

來源: Rabbit

外觀: Lyophilized or Liquid


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