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PANK2 抗体 (N-Term)

This anti-PANK2 antibody is a 兔 多克隆 antibody detecting PANK2 in WB. Suitable for 人.
产品编号 ABIN391237
发货至: 中国

Quick Overview for PANK2 抗体 (N-Term) (ABIN391237)

抗原

See all PANK2 抗体
PANK2 (Pantothenate Kinase 2 (PANK2))

适用

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宿主

  • 44
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克隆类型

  • 45
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多克隆

标记

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This PANK2 antibody is un-conjugated

应用范围

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Western Blotting (WB)

克隆位点

RB5486
  • 抗原表位

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    AA 65-95, N-Term

    纯化方法

    This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.

    免疫原

    This PANK2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 65-95 amino acids from the N-terminal region of human PANK2.

    亚型

    Ig Fraction
  • 应用备注

    WB: 1:1000

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    储存液

    Sodium azide

    注意事项

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

    储存条件

    4 °C,-20 °C

    储存方法

    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

    有效期

    6 months
  • 抗原

    PANK2 (Pantothenate Kinase 2 (PANK2))

    别名

    PANK2

    背景

    Pantothenate kinase is an essential regulatory enzyme in CoA biosynthesis, catalyzing the cytosolic phosphorylation of pantothenate (vitamin B5), N-pantothenoylcysteine, and pantetheine. CoA is the major acyl carrier, playing a central role in intermediary and fatty acid metabolism. In both yeast and fly, each with only 1 pantothenate kinase gene, the null mutant is inviable. Mutations in PANK2 are the cause of pantothenate kinase-associated neurodegeneration (PKAN), formerly known as Hallervorden-Spatz syndrome (HSS). PKAN is an autosomal recessive neurodegenerative disorder associated with iron accumulation in the brain. Mutations in PANK2 are the cause of hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration (HARP).

    分子量

    62681

    基因ID

    80025

    NCBI登录号

    NP_079236, NP_705902, NP_705904

    UniProt

    Q9BZ23

    途径

    Ribonucleoside Biosynthetic Process
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