KY Antibody, FITC conjugated
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中文名稱：KY兔多克隆抗體, FITC偶聯(lián)
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貨號(hào)：CSB-PA012702LC01HU
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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) KY Polyclonal antibody
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Uniprot No.：
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基因名：KY
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別名：KY antibody; KY_HUMAN antibody; Kyphoscoliosis peptidase 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 Kyphoscoliosis peptidase protein (23-170AA)
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免疫原種屬：Homo sapiens (Human)
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標(biāo)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(chǎn)品提供形式：Liquid
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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：Probable cytoskeleton-associated protease required for normal muscle growth. Involved in function, maturation and stabilization of the neuromuscular junction. May act by cleaving muscle-specific proteins such as FLNC.
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基因功能參考文獻(xiàn)：
- This study shown Kyphoscoliosis peptidase (KY) mutation causes a novel congenital myopathy with core targetoid defects in two bother. PMID: 27484770
- Homozygous KY mutation was identified as a cause of progressive hereditary spastic paraplegia. High KY transcript levels were demonstrated in muscular organs and lower expression in the CNS. PMID: 28488683
- Homozygous c.1071delG, p.(Thr358Leufs*3) variant of KY causes neuromuscular disorder by introducing a premature stop codon. PMID: 27485408
- KY expression is significantly downregulated in human masticatory mucosa during wound healing PMID: 28005267
- Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator) PMID: 20379614
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相關(guān)疾病：Myopathy, myofibrillar, 7 (MFM7)
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亞細(xì)胞定位：Cytoplasm, cytoskeleton. Cytoplasm, myofibril, sarcomere, Z line.
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蛋白家族：Transglutaminase-like superfamily
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組織特異性：Highly expressed in skeletal muscle.
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數(shù)據(jù)庫(kù)鏈接：
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