KY Antibody
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货号:CSB-PA012702LA01HU
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规格:¥440
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促销:
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图片:
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Western Blot
Positive WB detected in: Hela whole cell lysate, MCF-7 whole cell lysate, U87 whole cell lysate
All lanes: KY antibody at 3.2µg/ml
Secondary
Goat polyclonal to rabbit IgG at 1/50000 dilution
Predicted band size: 64, 42, 73, 76 kDa
Observed band size: 64 kDa -
Immunohistochemistry of paraffin-embedded human skeletal muscle tissue using CSB-PA012702LA01HU at dilution of 1:100
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Immunofluorescence staining of Hela cells with CSB-PA012702LA01HU at 1:133, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4°C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L).
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其他:
产品详情
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产品名称:Rabbit anti-Homo sapiens (Human) KY Polyclonal antibody
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Uniprot No.:Q8NBH2
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基因名:KY
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别名:KY antibody; KY_HUMAN antibody; Kyphoscoliosis peptidase antibody
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宿主:Rabbit
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反应种属:Human
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免疫原:Recombinant Human Kyphoscoliosis peptidase protein (23-170AA)
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免疫原种属:Homo sapiens (Human)
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标记方式:Non-conjugated
本页面中的产品,KY Antibody (CSB-PA012702LA01HU),的标记方式是Non-conjugated。对于KY Antibody,我们还提供其他标记。见下表:
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克隆类型:Polyclonal
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抗体亚型:IgG
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纯化方式:>95%, Protein G 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:Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4 -
产品提供形式:Liquid
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应用范围:ELISA, WB, IHC, IF
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推荐稀释比:
Application Recommended Dilution WB 1:500-1:5000 IHC 1:20-1:200 IF 1:50-1:200 -
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: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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基因功能参考文献:
- 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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相关疾病:Myopathy, myofibrillar, 7 (MFM7)
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亚细胞定位:Cytoplasm, cytoskeleton. Cytoplasm, myofibril, sarcomere, Z line.
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蛋白家族:Transglutaminase-like superfamily
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组织特异性:Highly expressed in skeletal muscle.
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数据库链接:
HGNC: 26576
OMIM: 605739
KEGG: hsa:339855
STRING: 9606.ENSP00000397598
UniGene: Hs.146730
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