WDR73 Antibody, HRP conjugated
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中文名稱：WDR73兔多克隆抗體, HRP偶聯(lián)
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貨號(hào)：CSB-PA744047LB01HU
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規(guī)格：￥880
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其他：
產(chǎn)品詳情
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產(chǎn)品名稱：Rabbit anti-Homo sapiens (Human) WDR73 Polyclonal antibody
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Uniprot No.：
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基因名：WDR73
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別名：WDR73 antibody; HSPC264WD repeat-containing protein 73 antibody
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宿主：Rabbit
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反應(yīng)種屬：Human
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免疫原：Recombinant Human WD repeat-containing protein 73 protein (163-366AA)
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免疫原種屬：Homo sapiens (Human)
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標(biāo)記方式：HRP
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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：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：Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4 -
產(chǎn)品提供形式：Liquid
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應(yīng)用范圍：ELISA
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Protocols：
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儲(chǔ)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(chǎn)品評(píng)價(jià)
相關(guān)產(chǎn)品
靶點(diǎn)詳情
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功能：May play a role in the regulation of microtubule organization and dynamics.
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基因功能參考文獻(xiàn)：
- We expanded the clinical phenotype of GMS with WDR73 gene defect to include retinal dysfunction with missense mutation and developmental dysplasia of the hip. PMID: 29929488
- WDR73 as a candidate gene of severe intellectual disability and cerebellar hypoplasia. PMID: 27983999
- We document postnatal onset of CA, a retinopathy, basal ganglia degeneration, and short stature as novel features of WDR73-related disease, and define WDR73-related disease as a new entity of infantile neurodegeneration. PMID: 26123727
- Nonsense mutation in the WDR73 gene is associated with Galloway-Mowat syndrome PMID: 25873735
- WDR73 interacts with mitotic microtubules to regulate cell cycle progression, proliferation and survival in brain PMID: 26070982
- WDR73 plays a crucial role in the maintenance of cell architecture and cell survival. PMID: 25466283
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相關(guān)疾病：Galloway-Mowat syndrome 1 (GAMOS1)
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亞細(xì)胞定位：Cytoplasm, cytosol. Cytoplasm, cytoskeleton, spindle. Cytoplasm, cytoskeleton, spindle pole. Cleavage furrow.
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蛋白家族：WD repeat WDR73 family
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組織特異性：Expressed in kidney and brain. In the kidney, expressed in glomeruli, most probably in podocytes, and in tubules (at protein level). In the brain, expressed in the cerebellum, with high levels in Purkinje cells and their projecting axons, in the deep cere
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