MPI Monoclonal Antibody
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中文名稱:MPI Monoclonal Antibody
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貨號:CSB-MA273467
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規格:¥1320
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圖片:
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Flow cytometric analysis of Mannose phosphate isomerase expression in HeLa cells using Mannose phosphate isomerase antibody. Green, isotype control; red, Mannose phosphate isomerase.
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Western blotting analysis using mannose phosphate isomerase antibody. Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with mannose phosphate isomerase antibody and HRP-conjugated goat mouse secondary antibody respectively.
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其他:
產品詳情
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產品名稱:Mouse anti-Homo sapiens (Human) MPI Monoclonal antibody
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Uniprot No.:
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基因名:MPI
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別名:MPI; Mannose Phosphate Isomerase; Mannose-6-Phosphate Isomerase; Phosphohexomutase; EC 5.3.1.8; PMI1; PMI; Phosphomannose Isomerase 1; Phosphomannose Isomerase; EC 5.3.1; CDG1B
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宿主:Mouse
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反應種屬:Human
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免疫原:Recombinant Human MPI protein
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免疫原種屬:Homo sapiens (Human)
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標記方式:Non-conjugated
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克隆類型:Monoclonal
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抗體亞型:Mouse IgG1
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純化方式:Affinity-chromatography
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克隆號:6D9
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濃度:It differs from different batches. Please contact us to confirm it.
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保存緩沖液:PBS (pH 7.4) containing 50% glycerol, and 0.02% sodium azide.
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產品提供形式:Liquid
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應用范圍:ELISA, WB, FC
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推薦稀釋比:
Application Recommended Dilution WB 1:1000-1:5000 FC 1:200-1:2000 -
Protocols:
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儲存條件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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貨期:Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
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用途:For Research Use Only. Not for use in diagnostic or therapeutic procedures.
相關產品
靶點詳情
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功能:Involved in the synthesis of the GDP-mannose and dolichol-phosphate-mannose required for a number of critical mannosyl transfer reactions.
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基因功能參考文獻:
- This work provides mechanistic evidence by which mannose phosphate isomerase loss induces p53, and identifies mannose phosphate isomerase as a novel regulator of p53 and Warburg metabolism. PMID: 28644127
- Phosphomannose isomerase inhibitors improve N-glycosylation in selected phosphomannomutase-deficient fibroblasts PMID: 21949237
- The mannose-6-phosphate-enzyme complex is developed and the key residues involved in the ligand binding are determined. Our results suggest a hydride transfer mechanism of alpha-hydrogen between the C1 and C2 positions. PMID: 16488169
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相關疾病:Congenital disorder of glycosylation 1B (CDG1B)
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亞細胞定位:Cytoplasm.
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蛋白家族:Mannose-6-phosphate isomerase type 1 family
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組織特異性:Expressed in all tissues, but more abundant in heart, brain and skeletal muscle.
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數據庫鏈接:
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