UROD Antibody
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货号:CSB-PA025678GA01HU
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规格:¥3,900
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其他:
产品详情
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Uniprot No.:P06132
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基因名:UROD
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别名:DCUP_HUMAN antibody; PCT antibody; UPD antibody; URO D antibody; URO-D antibody; urod antibody; Uroporphyrinogen decarboxylase antibody; Uroporphyrinogen III decarboxylase antibody
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宿主:Rabbit
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反应种属:Human,Mouse,Rat
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免疫原:Human UROD
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免疫原种属:Homo sapiens (Human)
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抗体亚型:IgG
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纯化方式:Antigen Affinity purified
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浓度:It differs from different batches. Please contact us to confirm it.
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保存缓冲液:PBS with 0.1% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
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产品提供形式:Liquid
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应用范围:ELISA,WB
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Protocols:
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储存条件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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货期: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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靶点详情
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功能:Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III.
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基因功能参考文献:
- a new mutation in the UROD gene in Egyptian patients with Hepatoerythropoietic porphyria, is reported. PMID: 26789143
- a new insight in the conformational changes occurred in the mutant structures of UROD protein. PMID: 24777812
- Data suggest that the traditional Chinese medicine (TCM) candidate potential three-in-one inhibitors for three drug target proteins epidermal growth factor receptor (EGFR), Her2, and uroporphyrinogen decarboxylase (UROD) against head and neck cancer. PMID: 23140436
- Expression of the D306Y mutation results in an insoluble recombinant protein. G318R and K297N have little effect on the structure or activity of recombinant URO-D, but the proteins display reduced stability in vitro. PMID: 19656450
- Among seventeen F-PCT patients, sixteen UROD mutations were identified. PMID: 23545314
- analysis of uroporphyrinogen decarboxylase as a potential target for specific components of traditional Chinese medicine PMID: 23209648
- Mutations in UROD gene is associated with familial porphyria cutanea tarda. PMID: 22382040
- Hepatoerythropoietic porphyria and familial porphyria cutanea tarda G281E mutation in the uroporphyrinogen decarboxylase gene PMID: 21079081
- function of Arg37 in uroporphyrinogen III decarboxylase PMID: 20553007
- description of 3 siblings with hepatoerythropoietic porphyria; sequencing of the UROD gene revealed compound heterozygosity for a novel missense mutation, V166A, and a complex deletion/insertion, 645del1053ins10 PMID: 20479301
- Sequence deletions in uroporphyrinogen decarboxylase is associated with Porphyria Cutanea Tarda. PMID: 15046048
- we identified eight mutations in 18 previously unclassified porphyria cutanea tarda families PMID: 15186324
- Sequencing of the hydroxymethylbilane synthase and uroporphyrinogen decarboxylase genes confirmed the relatively rare diagnosis of dual porphyria, and revealed a novel uroporphyrinogen decarboxylase mutation PMID: 16390615
- There is a high degree of molecular heterogeneity of familial porphyria cutanea tarda in Spain and molecular genetic analysis is useful in distinguish between F-PCT and sporadic PCT. PMID: 17627795
- role of UROD mutations as a strong risk factor for porphyria cutanea tarda even in areas where environmental factors (hepatitis C virus) have been shown to be highly associated with the disease PMID: 19419417
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相关疾病:Familial porphyria cutanea tarda (FPCT); Hepatoerythropoietic porphyria (HEP)
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亚细胞定位:Cytoplasm.
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蛋白家族:Uroporphyrinogen decarboxylase family
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数据库链接:
HGNC: 12591
OMIM: 176100
KEGG: hsa:7389
STRING: 9606.ENSP00000246337
UniGene: Hs.78601
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