Analytical Data
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基因名
PMM2
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简介
The PMM2 protein is essential for the synthesis of GDP-mannose and polyethylene glycol-phosphate-mannose, which are essential for the mannosyl transfer reaction. Its enzymatic activity is integral to the biosynthesis of mannose-containing glycoconjugates, affects protein glycosylation and contributes to cellular homeostasis. PMM2 Protein, Human (His) is the recombinant human-derived PMM2 protein, expressed by E. coli , with C-6*His labeled tag.
- Application
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别名
Phosphomannomutase 2; PMM 2; PMM2
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种属
Human
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表达系统
E. coli
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标签
C-6*His
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纯度
Greater than 90% as determined by SDS-PAGE.
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蛋白编号
O15305-1
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表达区间
M1-S246
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氨基酸序列
MAAPGPALCLFDVDGTLTAPRQKITKEMDDFLQKLRQKIKIGVVGGSDFEKVQEQLGNDVVEKYDYVFPENGLVAYKDGKLLCRQNIQSHLGEALIQDLINYCLSYIAKIKLPKKRGTFIEFRNGMLNVSPIGRSCSQEERIEFYELDKKENIRQKFVADLRKEFAGKGLTFSIGGQISFDVFPDGWDKRYCLRHVENDGYKTIYFFGDKTMPGGNDHEIFTDPRTMGYSVTAPEDTRRICELLFS
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蛋白长度
Full Length of Isoform-1
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分子量
29 kDa
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内毒素
< 1.0 EU per μg protein as determined by the LAL method.
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性状
Freeze-dried powder
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缓冲液
PBS, pH7.4, containing 0.01% SKL, 1mM DTT, 5% Trehalose and Proclin300.
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复溶方法
Reconstitute in ddH2O to a concentration of 0.1-0.5 mg/mL. Do not vortex.
- 个性化定制
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稳定性测试
The thermal stability is described by the loss rate. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37℃ for 48h, and no obvious degradation and precipitation were observed. The loss rate isless than 8% within the expiration date under appropriate storage condition.
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保存条件 & 期限
Samples are stable for up to twelve months from date of receipt at -20℃ to -80℃. Store it under sterile conditions at -20℃ to -80℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
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运输条件
In general, recombinant proteins are supplied as lyophilized powder and shipped at ambient temperature. For bulk packages, the proteins are provided as frozen liquid and shipped with blue ice, unless otherwise requested by the customer.
Quality inspection process
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Protein Description
PMM2, or Phosphomannomutase 2, is an enzyme that plays a crucial role in the metabolism of monosaccharides, specifically in the conversion of mannose-6-phosphate to mannose-1-phosphate, a key step in glycosylation and cell wall synthesis in various organisms. Mutations in the PMM2 gene are linked to Congenital Disorder of Glycosylation type Ia (CDG-Ia), a severe genetic condition characterized by a range of developmental and neurological impairments, indicating the enzyme's vital role in human health. Research on recombinant PMM2 proteins has garnered attention due to their potential applications in understanding disease mechanisms and developing therapeutic strategies. The production of recombinant PMM2 allows researchers to investigate the functional consequences of specific mutations, evaluate enzyme kinetics, and explore its structural properties. Moreover, studying PMM2 in vitro provides insights into the biochemical pathways affected by its deficiency and paves the way for gene therapy approaches to correct the underlying genetic defect. As such, the development of PMM2 recombinant proteins is essential not only for advancing our knowledge of CDG-Ia but also for exploring broader implications in glycosylation disorders and personalized medicine approaches targeting genetic diseases.
