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ATP13A2 抗体 (PE)

This 兔 多克隆 antibody specifically detects ATP13A2 in IF (cc) 和 IF (p). It exhibits reactivity toward 人.
产品编号 ABIN1427815
发货至: 中国
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Quick Overview for ATP13A2 抗体 (PE) (ABIN1427815)

抗原

See all ATP13A2 抗体
ATP13A2 (ATPase Type 13A2 (ATP13A2))

适用

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宿主

  • 31
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克隆类型

  • 32
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多克隆

标记

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This ATP13A2 antibody is conjugated to PE

应用范围

  • 15
  • 13
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  • 11
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  • 1
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Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 原理

    ATP13A2 Polyclonal Antibody, PE Conjugated

    交叉反应

    大鼠

    预测反应

    Human,Mouse,Cow,Pig,Horse,Rabbit

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human ATP13A2

    亚型

    IgG
  • 应用备注

    IF(IHC-P)(1:50-200), IF(IHC-F)(1:50-200), IF(ICC)(1:50-200)

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 μg/μL

    缓冲液

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

    储存液

    ProClin

    注意事项

    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    储存条件

    -20 °C

    储存方法

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    有效期

    12 months
  • 抗原

    ATP13A2 (ATPase Type 13A2 (ATP13A2))

    别名

    Park9/Atp13a2

    背景

    Synonyms: 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.

    Background: 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.

    途径

    Ribonucleoside Biosynthetic Process
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