NXF5 Antibody
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货号:CSB-PA016223LA01HU
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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
All lanes: NXF5 antibody at 4µg/ml + HL60 whole cell lysate
Secondary
Goat polyclonal to rabbit IgG at 1/10000 dilution
Predicted band size: 46, 43, 20, 36, 35 kDa
Observed band size: 46 kDa -
Immunohistochemistry of paraffin-embedded human prostate cancer using CSB-PA016223LA01HU at dilution of 1:100
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Immunofluorescent analysis of HepG2 cells using CSB-PA016223LA01HU at dilution of 1:100 and Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L)
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Immunohistochemistry of paraffin-embedded human colon cancer using CSB-PA016223LA01HU at dilution of 1:100
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其他:
产品详情
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产品名称:Rabbit anti-Homo sapiens (Human) NXF5 Polyclonal antibody
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Uniprot No.:Q9H1B4
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基因名:NXF5
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别名:NXF5 antibody; TAPL1 antibody; Nuclear RNA export factor 5 antibody; TAP-like protein 1 antibody; TAPL-1 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 Nuclear RNA export factor 5 protein (1-200AA)
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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,NXF5 Antibody (CSB-PA016223LA01HU),的标记方式是Non-conjugated。对于NXF5 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 1:500-1:2000 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:Could be involved in the export of mRNA from the nucleus to the cytoplasm. Could also have a role in polarized cytoplasmic transport and localization of mRNA in neurons.
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基因功能参考文献:
- study of an Australian pedigree in which focal segmental glomerulosclerosis co-segregates with progressive heart block; study found 2 mutations NXF5-R113W and ALG13-T141L segregated with disease phenotype; predicted the NXF5 R113W mutation to be deleterious; cellular studies support a role in the stability and localization of the protein suggesting a causative role PMID: 23686279
- Mutations of the NXF5 gene is associated with X-linked mental retardation PMID: 12784308
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相关疾病:A chromosomal aberration involving NXF5 has been observed in one patient with a syndromic form of mental retardation and short stature. Pericentric inversion inv(X)(p21.1;q22) that interrupts NXF5.
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亚细胞定位:Cytoplasm. Nucleus. Note=Mainly localized in the cytoplasm of cells and more particularly in the cell body and neurites of hippocampal neurons. Although nuclear localization is also observed. Not detected at nuclear rim.
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蛋白家族:NXF family
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数据库链接:
HGNC: 8075
OMIM: 300319
KEGG: hsa:55998
STRING: 9606.ENSP00000426978
UniGene: Hs.307077
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