ACP2 Antibody
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								中文名稱:ACP2兔多克隆抗體
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								貨號:CSB-PA001177GA01HU
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								規格:¥3,900
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								其他:
產品詳情
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											Uniprot No.:
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											基因名:ACP2
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											別名:ACP2; Lysosomal acid phosphatase; LAP
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											宿主:Rabbit
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											反應種屬:Human,Mouse,Rat
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											免疫原:Human ACP2
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											免疫原種屬:Homo sapiens (Human)
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											抗體亞型:IgG
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											純化方式:Antigen Affinity purified
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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 with 0.02% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
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											產品提供形式:Liquid
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											應用范圍:ELISA,WB
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											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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											基因功能參考文獻:- In addition to replicating a previously identified genome-wide significant locus for corneal astigmatism near the PDGFRA gene, gene-based analysis identified three novel candidate genes, CLDN7, ACP2, and TNFAIP8L3, that warrant further investigation to understand their role in the pathogenesis of corneal astigmatism. (Meta-analysis) PMID: 29422769
- Data show that lysosomal acid phosphatase 2 (ACP2) was overexpressed in colorectal cancer (CRC) and associated with poor outcome in stage II CRC, and that high expression of ACP2 patients were more sensitive to chemotherapy than those with a low expression, suggesting ACP2 as a marker for CRC patients receiving chemotherapy. PMID: 28076332
- An enzymatically inactive allele of mouse Acp2 causes cerebellum abnormalities, growth retardation, hair-follicle abnormalities, and an ataxia-like phenotype. PMID: 15503243
- LAP-deficient mice exhibit multiple defects including bone structure alterations, lysosomal storage defects in the kidneys and central nervous system, and an increased tendency towards seizures. PMID: 9228031
- Genome-wide association study of gene-disease association. (HuGE Navigator) PMID: 17357082
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											相關疾病:Lysosomal acid phosphatase has been shown to be deficient in cultured fibroblasts from patients manifesting intermittent vomiting, hypotonia, lethargy, opisthotonos, terminal bleeding and death in early infancy.
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											亞細胞定位:Lysosome membrane; Single-pass membrane protein; Lumenal side. Lysosome lumen.
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											蛋白家族:Histidine acid phosphatase family
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											數據庫鏈接:
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