4)经纯化制备的抗体在常用的缓冲液中是稳定的。其DH应保持在中性左右。如果pH在7-8之间,即使保存多年,对抗体也无损害。多数情况下,盐浓度适于保持在0-150mmol/L之间,但在长期存放的抗体中,盐溶液浓度高达500mmol/L时,对
抗体来源 Rabbit
克隆类型 polyclonal
交叉反应 Human, Mouse, Rat, Chicken, Dog, Pig, Cow, Horse, Rabbit
产品类型 一抗
研究领域 细胞生物 免疫学 神经生物学 表观遗传学
蛋白分子量 predicted molecular weight: 74kDa
性 状 Lyophilized or Liquid
免 疫 原 KLH conjugated synthetic peptide derived from human FXR2
亚 型 IgG
纯化方法 affinity purified by Protein A
储 存 液 Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4
产品应用 WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:50-200
(石蜡切片需做抗原修复)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
保存条件 Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
Important Note This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
脆性X相关蛋白样2抗体产品介绍 Fragile X syndrome is caused by the absence of the fragile X mental-retardation protein (FMRP). FMRP is the archetype of a class of cytoplasmic mRNA-binding proteins that includes the fragile X-related 1 and 2 proteins (FXR1 and FXR2). The fragile X-related proteins FXR1 and FXR2 contain a functional nucleolar-targeting signal equivalent to the HIV-1 regulatory proteins.
Subunit : Interacts with FMR1 and FXR1. Interacts with CYFIP2 but not with CYFIP1. Interacts with TDRD3.
Subcellular Location : Cytoplasm.
Similarity : Belongs to the FMR1 family.
Contains 2 Agenet-like domains.
Contains 2 KH domains.
脆性X综合症,又称马丁-贝尔综合症,是一种遗传疾病。该综合症可以导致一系列的特征性症状,包括生理、智力、情绪、以及行为上的异常。症状的轻重各有不同。该疾病伴随着X染色体上一个简单的三核苷酸基因序列(CGG)的扩增。这种扩增导致了一种称为FMR-1的蛋白质无法在病人体内表达,而该蛋白质是神经的正常发育必不可少的。
根据CGG重复序列的长度,目前普遍认可将脆性X综合症分为四种类型:正常人(含有19-31个CGG重复序列),前突变者(含有55-200个CGG重复序列),全突变者(含有200个以上的CGG重复序列),过渡型,又称“灰色区域型”(含有40-60个重复)。脆性X综合征这是一种导致智力低下的遗传疾病,是导致人群中智力低下的第二大病因——仅次于21三体综合症。