NHP2 Antibody, FITC conjugated
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中文名稱：NHP2兔多克隆抗體, FITC偶聯
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貨號：CSB-PA873677LC01HU
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規格：￥880
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其他：
產品詳情
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產品名稱：Rabbit anti-Homo sapiens (Human) NHP2 Polyclonal antibody
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Uniprot No.：
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基因名：NHP2
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別名：DKCB2 antibody; FLJ20479 antibody; H/ACA ribonucleoprotein complex subunit 2 antibody; NHP2 antibody; NHP2 like protein antibody; NHP2 ribonucleoprotein antibody; NHP2 ribonucleoprotein homolog (yeast) 1 antibody; NHP2 ribonucleoprotein homolog antibody; NHP2; S. cerevisiae; homolog of antibody; NHP2_HUMAN antibody; NHP2P antibody; NOLA2 antibody; Nucleolar protein family A member 2 (H/ACA small nucleolar RNPs) antibody; Nucleolar protein family A member 2 antibody; snoRNP protein NHP2 antibody
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宿主：Rabbit
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反應種屬：Human
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免疫原：Recombinant Human H/ACA ribonucleoprotein complex subunit 2 protein (1-153AA)
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免疫原種屬：Homo sapiens (Human)
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標記方式：FITC
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克隆類型：Polyclonal
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抗體亞型：IgG
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純化方式：>95%, Protein G 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：Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, PH 7.4 -
產品提供形式：Liquid
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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.
產品評價
相關產品
靶點詳情
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功能：Required for ribosome biogenesis and telomere maintenance. Part of the H/ACA small nucleolar ribonucleoprotein (H/ACA snoRNP) complex, which catalyzes pseudouridylation of rRNA. This involves the isomerization of uridine such that the ribose is subsequently attached to C5, instead of the normal N1. Each rRNA can contain up to 100 pseudouridine ('psi') residues, which may serve to stabilize the conformation of rRNAs. May also be required for correct processing or intranuclear trafficking of TERC, the RNA component of the telomerase reverse transcriptase (TERT) holoenzyme.
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基因功能參考文獻：
- In this work, we have uncovered a putative role of epigenetic regulation in a subset of human snoRNP complexes that are involved in the site-specific modification of RNA. We find that a subset of box C/D snoRNAs are methylated at the 1n position and that this blocks both 15.5k binding and the formation of the kinked conformation in vivo. PMID: 28623187
- Indian aplastic anemia patients did not have NHP2 mutations. PMID: 25906515
- Effects of dyskeratosis congenita mutations in NHP2 on assembly of H/ACA pre-RNPs PMID: 20008900
- NOLA2 expression in patients with squamous cell lung cancer increased by 70% which makes it a highly informative marker of squamous cell lung cancer PMID: 15889794
- The analysis of two other proteins, NHP2 and GAR1, that together with dyskerin and NOP10 are key components of telomerase and small nucleolar ribonucleoprotein (snoRNP) complexes, is described. PMID: 18523010
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相關疾病：Dyskeratosis congenita, autosomal recessive, 2 (DKCB2)
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亞細胞定位：Nucleus, nucleolus. Nucleus, Cajal body. Note=Also localized to Cajal bodies (coiled bodies).
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蛋白家族：Eukaryotic ribosomal protein eL8 family
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組織特異性：Expressed in brain, colon, heart, kidney, ovary, pancreas, placenta, prostate, skeletal muscle, small intestine, spleen, testis and thymus. Also expressed at lower levels in the liver.
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數據庫鏈接：
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