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GPI 抗体 (AA 2-39)

This anti-GPI antibody is a 兔 多克隆 antibody detecting GPI in WB. Suitable for 小鼠.
产品编号 ABIN5647568
发货至: 中国

Quick Overview for GPI 抗体 (AA 2-39) (ABIN5647568)

抗原

See all GPI 抗体
GPI (Glucose-6-Phosphate Isomerase (GPI))

适用

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小鼠

宿主

  • 96
  • 27
  • 1

克隆类型

  • 88
  • 36
多克隆

标记

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This GPI antibody is un-conjugated

应用范围

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Western Blotting (WB)
  • 抗原表位

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    AA 2-39

    纯化方法

    Antigen affinity purified

    免疫原

    Amino acids 2-39 (AALTRNPQFQKLLEWHRANSANLKLRELFEADPERFNN) from the mouse protein were used as the immunogen for the Glucose-6-phosphate isomerase antibody.

    亚型

    IgG
  • 应用备注

    Western blot: 0.5-1 μg/mL

    限制

    仅限研究用
  • 缓冲液

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    储存条件

    -20 °C

    储存方法

    After reconstitution, the Glucose-6-phosphate isomerase antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • 抗原

    GPI (Glucose-6-Phosphate Isomerase (GPI))

    别名

    GPI / Glucose-6-phosphate isomerase

    背景

    Glucose-6-phosphate isomerase (GPI), alternatively known as phosphoglucose isomerase (PGI) or phosphohexose isomerase (PHI), is an enzyme that in humans is encoded by the GPI gene on chromosome 19. This gene encodes a member of the glucose phosphate isomerase protein family. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. In the cytoplasm, the gene product functions as a glycolytic enzyme (glucose-6-phosphate isomerase) that interconverts glucose-6-phophsate and fructose-6-phosphate. Extracellularly, the encoded protein (also referred to as neuroleukin) functions as a neurotrophic factor that promotes survival of skeletal motor neurons and sensory neurons, and as a lymphokine that induces immunoglobulin secretion. The encoded protein is also referred to as autocrine motility factor based on an additional function as a tumor-secreted cytokine and angiogenic factor. Defects in this gene are the cause of nonspherocytic hemolytic anemia and a severe enzyme deficiency can be associated with hydrops fetalis, immediate neonatal death and neurological impairment. Alternative splicing results in multiple transcript variants.

    UniProt

    P06745
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