LHFPL5 Antibody
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货号:CSB-PA844703LA01HU
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规格:¥440
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促销:
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图片:
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Immunohistochemistry of paraffin-embedded human testis tissue using CSB-PA844703LA01HU at dilution of 1:100
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Immunohistochemistry of paraffin-embedded human skeletal muscle tissue using CSB-PA844703LA01HU at dilution of 1:100
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Immunofluorescent analysis of A549 cells using CSB-PA844703LA01HU at dilution of 1:100 and 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) LHFPL5 Polyclonal antibody
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Uniprot No.:Q8TAF8
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基因名:LHFPL5
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别名:LHFPL5; TMHS; LHFPL tetraspan subfamily member 5 protein; Lipoma HMGIC fusion partner-like 5 protein; Tetraspan membrane protein of hair cell stereocilia
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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 LHFPL tetraspan subfamily member 5 protein (46-99AA)
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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,LHFPL5 Antibody (CSB-PA844703LA01HU),的标记方式是Non-conjugated。对于LHFPL5 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, IHC, IF
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推荐稀释比:
Application Recommended Dilution 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.
相关产品
靶点详情
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功能:In the inner ear, may be a component of the hair cell's mechanotransduction machinery that functionally couples PCDH15 to the transduction channel. Regulates transducer channel conductance and is required for fast channel adaptation.
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基因功能参考文献:
- two novel variants in LHFPL5, including a unique 3'-UTR splice site variant that is predicted to impact pre-mRNA splicing and regulation through an extended 3'-UTR. PMID: 30177809
- These findings provide a novel function of LHFPL2 and a novel genetic basis for distal reproductive tract development; they also emphasize the importance of an additional merging phase for proper reproductive tract development. PMID: 26964900
- LHFPL5 mutation is associated with dysequilibrium syndrome type 2 and sensorineural hearing loss. PMID: 26437881
- Five microsatellites in the 6p21.31e22.3 region and screening of the LHFPL5 gene by DNA heteroduplex analysis revealed a novel mutation (c.89dup) in one out of 129 unrelated Tunisian families with autosomal recessive nonsyndromic hearing loss. PMID: 21816241
- These findings establish the importance of TMHS for normal sound transduction in humans. PMID: 16459341
- Flies with mutations affecting the diaphanous,forked, and CG12026/TMHS genes displayed significant reductions in the amplitude of sound-evoked potentials compared to wild-type flies PMID: 19102128
- The s present an overview of the LHFP gene family in mouse and humans PMID: 15905332
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相关疾病:Deafness, autosomal recessive, 67 (DFNB67)
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亚细胞定位:Cell membrane; Multi-pass membrane protein.
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蛋白家族:LHFP family
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数据库链接:
HGNC: 21253
OMIM: 609427
KEGG: hsa:222662
STRING: 9606.ENSP00000353346
UniGene: Hs.367947
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