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ATL1 Protein (GST tag)

ATL1 宿主: 人 宿主: Baculovirus infected Insect Cells Recombinant > 80 % as determined by reducing SDS-PAGE.
产品编号 ABIN7194321
发货至: 中国
  • 抗原 See all ATL1 蛋白
    ATL1 (Atlastin GTPase 1 (ATL1))
    蛋白类型
    Recombinant
    宿主
    • 4
    • 2
    资源
    • 2
    • 2
    • 1
    • 1
    Baculovirus infected Insect Cells
    标记
    This ATL1 protein is labelled with GST tag.
    原理
    Recombinant Human ATL1/SPG3A/Atlastin-1 Protein (GST Tag)
    序列
    Met 1-Thr 447
    产品特性
    A DNA sequence encoding the human SPG3A (NP_056999.2) (Met 1-Thr 447) was fused with the GST tag at the N-terminus.
    纯度
    > 80 % as determined by reducing SDS-PAGE.
    内毒素水平
    < 1.0 EU per μg as determined by the LAL method.
    Top Product
    Discover our top product ATL1 蛋白
  • 限制
    仅限研究用
  • 状态
    Lyophilized
    溶解方式
    Please refer to the printed manual for detailed information.
    缓冲液
    Lyophilized from sterile 50 mM Tris, 100 mM NaCl, 0.5 mM PMSF, 0.5 mM EDTA, 0.5 mM GSH, pH 8.0
    储存条件
    4 °C,-20 °C,-80 °C
    储存方法
    Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80°C. Reconstituted protein solution can be stored at 4-8°C for 2-7 days. Aliquots of reconstituted samples are stable at < -20°C for 3 months.
  • 抗原
    ATL1 (Atlastin GTPase 1 (ATL1))
    别名
    ATL1/SPG3A/Atlastin-1 (ATL1 产品)
    别名
    ATL1 Protein, SPG3A Protein, fj46c01 Protein, wu:fj46c01 Protein, spg3a Protein, MGC146251 Protein, AD-FSP Protein, FSP1 Protein, GBP3 Protein, HSN1D Protein, SPG3 Protein, atlastin1 Protein, 4930435M24Rik Protein, Adfsp Protein, Fsp1 Protein, Spg3 Protein, Spg3a Protein, atlastin Protein, Atlastin-1 Protein, atlastin GTPase 1 Protein, ATL1 Protein, atl1 Protein, Atl1 Protein
    背景

    Background: Atlastin-1, also known as Spastic paraplegia 3 protein A, Guanine nucleotide-binding protein 3, GTP-binding protein 3, GBP3, ATL1 and SPG3A, is a multi-pass membrane protein which belongs to the GBP family and atlastin subfamily. ATL1 / SPG3A is expressed predominantly in the adult and fetal central nervous system. Expression of ATL1 / SPG3A in adult brain is at least 50-fold higher than in other tissues. ATL1 / SPG3A is detected predominantly in pyramidal neurons in the cerebral cortex and the hippocampus of the brain. ATL1 / SPG3A is also expressed in upper and lower motor neurons (at protein level). A distinguishing feature of ATL1 / SPG3A is its frequent early onset, raising the possibility that developmental abnormalities may be involved in its pathogenesis. Missense SPG3A mutant atlastin-1 proteins have impaired GTPase activity and may act in a dominant-negative, loss-of-function manner by forming mixed oligomers with wild-type atlastin-1. Defects in ATL1 / SPG3A are the cause of spastic paraplegia autosomal dominant type 3 (SPG3), also known as Strumpell-Lorrain syndrome. Spastic paraplegia is a degenerative spinal cord disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs.

    Synonym: AD-FSP;atlastin1;FSP1;GBP3;HSN1D;SPG3;SPG3A

    分子量
    77 kDa
    NCBI登录号
    NP_056999
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