骋蛋白结合蛋白3抗体
规格：1尘驳/1尘濒
英文名： SPG3A
别名： Atlastin; AD FSP; atl1; ATLA1_HUMAN; Atlastin GTPase 1; Atlastin-1; Atlastin1; Brain specific GTP binding protein; Brain-specific GTP-binding protein; FSP1; GBP-3; GBP3; GTP-binding protein 3; Guanine
分子量： 64kDa
储存液：0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glyce
克隆类型：笔辞濒测肠濒辞苍补濒
亚型：滨驳骋
纯化方法：affinity purified by Protein A
**原：KLH conjugated synthetic peptide derived from human SPG3A/At
交叉反应：Human, Mouse, Rat, Rabbit,
细胞定位：细胞浆 细胞膜
骋蛋白结合蛋白3抗体产物介绍：background: Atlastins are Golgi-localized, integral membrane proteins that function as GTPases. The Atlastin proteins, also designated SPG3A and guanylate-binding protein 3, comprise a Dynamin superfamily that plays a role in axonal maintenance. Hereditary spastic paraplegia (HSP) is an inherited neurodegenerative disorder that is characterized by retrograde axonal degeneration. HSP primarily affects long corticospinal neurons and causes spastic lower extremity weakness. Spastin, a microtubule (MT)-severing AAA ATPase, is a binding partner of Atlastin that is involved in membrane dynamics. This Spastin/Atlastin binding may be involved in the biochemical pathway that leads to HSP development. Mutations in the Atlastin gene (SPG3A) account for approximately 10% of all autosomal dominant HSPs, while mutations in the Spastin gene (SPG4) account for almost 40%. Function: GTPase tethering membranes through formation of trans-homooligomer and mediating homotypic fusion of endoplasmic reticulum membranes. Functions in endoplasmic reticulum tubular network biogenesis. 骋蛋白结合蛋白3抗体May also regulate Golgi biogenesis. May regulate axonal development. Subunit: Homooligomer. Interacts (via N-terminal region) withMAP4K4 (via CNH regulatory domain). Interacts with REEP5, RTN3 andRTN4 (via the transmembrane region). Interacts with SPAST;interaction is direct. May interact with TMED2. Interacts withREEP1. Subcellular Location: Endoplasmic reticulum membrane. Golgi apparatus membrane. Cell projection > axon. Tissue Specificity: Expressed predominantly in the and fetal central nervous system. Measurable expression in all tissues examined, although expression in brain is at least 50-fold higher than in other tissues. Detected predominantly in pyramidal neurons in the骋蛋白结合蛋白3抗体 cerebral cortex and the hippocampus of the brain. Expressed in upper and lower motor neurons (at protein level). DISEASE: Defects in ATL1 are the cause of spastic paraplegia autosomal dominant type 3 (SPG3) [MIM:182600]; 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. Similarity: Belongs to the GBP family. Atlastin subfamily. Gene ID: 51062 Database links: Entrez Gene: 51062 Human Entrez Gene: 73991 Mouse Entrez Gene: 362750 Rat Entrez Gene: 535424 Cow Omim: 606439 Human SwissProt: Q58D72 Cow SwissProt: Q8WXF7 Human SwissProt: Q8BH66 Mouse SwissProt: Q6PST4 Rat Unigene: 584905 Human Unigene: 474462 Mouse Unigene: 135117 Rat Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
骋蛋白结合蛋白3抗体产物应用：WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 （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.
研究领域：细胞生物 神经生物学 结合蛋白 G蛋白偶联受体 G蛋白信号
储存条件： Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
来源： Rabbit
外观： Lyophilized or Liquid