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Anti-GLB1L3 Polyclonal Antibody

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货号 TMAB-06498

Anti-GLB1L3 Polyclonal Antibody 是一种 Rabbit 抗体,靶向 GLB1L3。Anti-GLB1L3 Polyclonal Antibody 可用于 WB。

Anti-GLB1L3 Polyclonal Antibody

Anti-GLB1L3 Polyclonal Antibody

一键复制产品信息
Rating icon 还可以
货号 TMAB-06498

Anti-GLB1L3 Polyclonal Antibody 是一种 Rabbit 抗体,靶向 GLB1L3。Anti-GLB1L3 Polyclonal Antibody 可用于 WB。

规格价格库存数量
50 μL
¥ 1,170
5日内发货
100 μL
¥ 1,975
5日内发货
200 μL
¥ 2,790
5日内发货
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产品介绍


生物活性
产品描述
Anti-GLB1L3 Polyclonal Antibody is a Rabbit antibody targeting GLB1L3. Anti-GLB1L3 Polyclonal Antibody can be used in WB.
Ig Type
IgG
反应种属
Mouse (predicted:Human,Rat,Chicken,Horse)
应用WB
推荐剂量
WB: 1:500-2000
抗体种类
Polyclonal
宿主来源Rabbit
构建方式Hybridoma Polyclonal Antibody
纯化方式Protein A purified
性状Liquid
缓冲液0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
浓度1mg/ml
研究背景GLB1L3 is a 653 amino acid protein belonging to the glycosyl hydrolase 35 family. GLB1L3 exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11q25. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
抗原信息
免疫原
KLH conjugated synthetic peptide: human GLB1L3
抗原种属
Human
基因名称
GLB1L3
基因ID
蛋白名称
beta-galactosidase-1-like protein 3
Uniprot ID
化学信息
分子量Theoretical: 75 kDa.
储存&溶解度
储存方式Store at 2°C-8°C for 1 month. Store at -20°C or -80°C for 12 months. Avoid repeated freeze-thaw cycles.
运输方式Shipping with blue ice.
存储store at low temperature | -20°C for 1 year

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