帕金森病相关蛋白ATP13A2抗体

公司帕金森病相关蛋白ATP13A2抗体具有高纯度、高效价、高特异性的特点，仅用于科学研究，不可用于临床诊断及药物治疗，可以应用于多种实验。CST、Santa抗体品牌。

英文名称  Anti-PARK9/ATP13A2 

中文名称  帕金森病相关蛋白ATP13A2抗体 

别    名  AT132_HUMAN; Atp13a2; ATPase type 13A2; CLN12; HSA9947; KRPPD; PARK9; Probable cation transporting ATPase 13A2; Probable cation-transporting ATPase 13A2; Putative ATPase; RP1-37C10.4. 

浓    度  1mg/1ml 

规 格  0.2ml/200μg
帕金森病相关蛋白ATP13A2抗体 的相关产品:

Rabbit Anti-Mink IgG/AP  碱性磷酸酶（AP）标记的兔抗水貂IgG 0.1ml

Rabbit Anti-Mink IgG/APC  APC标记的兔抗水貂IgG 0.1ml

Rabbit Anti-Mink IgG/Bio  生物素标记的兔抗水貂IgG 0.1ml 

帕金森病相关蛋白ATP13A2抗体抗体来源  Rabbit  

克隆类型  polyclonal 

交叉反应  Human, Mouse, Rat, Pig, Cow, Horse, Rabbit 

产品类型  一抗    

研究领域  肿瘤 神经生物学 信号转导 细胞膜蛋白 Alzheimer's  

蛋白分子量  predicted molecular weight: 129kDa 

性    状  Lyophilized or Liquid 

免 疫 原  KLH conjugated synthetic peptide derived from human ATP13A2 (1001-1080aa) 

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  Flow-Cyt=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.  

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. 

产品介绍 ATP13A2 is a 1,180 amino acid multi-pass membrane protein that belongs to the P5 subfamily of ATPases which play an important role in the transportation of inorganic cations. Expressed as multiple alternative spliced isoforms, ATP13A2 functions to catalyze the conversion of ATP to ADP and a free phosphate, thereby participating in the active transport of ions across cellular membranes. Defects in the gene encoding ATP13A2 are the cause of Kufor-Rakeb syndrome (KRS), a rare hereditary type of Parkinson’s disease that exhibits juvenile onset and is characterized by neurodegeneration and dementia. The ATP13A2 gene maps to human chromosome 1, which spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8% of the human genome.

Function : May play a role in intracellular cation homeostasis and the maintenance of neuronal integrity. 

Subcellular Location : Membrane; Multi-pass membrane protein (By similarity). Lysosome. 

Tissue Specificity : Expressed in brain; protein levels are markedly increased in brain from subjects with Parkinson disease and subjects with dementia with Lewy bodies. Detected in pyramidal neurons located throughout the cingulate cortex (at protein level). In the substantia nigra, it is found in neuromelanin-positive dopaminergic neurons (at protein level). 

DISEASE : Defects in ATP13A2 are the cause of Kufor-Rakeb syndrome (KRS) [MIM:606693]; also known as Parkinson disease type 9 (PARK9). KRS is a rare hereditary disease with juvenile onset. In addition to typical signs of Parkinson disease, affected individuals show symptoms of more widespread 帕金森病相关蛋白ATP13A2抗体neurodegeneration, including dementia.

Similarity : Belongs to the cation transport ATPase (P-type) (TC 3.A.3) family. Type V subfamily.

Database links : UniProtKB/Swiss-Prot: Q9NQ11.2

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