ZNF335 Antibody
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货号:CSB-PA026683LA01HU
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规格:¥440
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促销:
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图片:
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其他:
产品详情
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产品名称:Rabbit anti-Homo sapiens (Human) ZNF335 Polyclonal antibody
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Uniprot No.:Q9H4Z2
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基因名:ZNF335
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别名:ZNF335 antibody; Zinc finger protein 335 antibody; NRC-interacting factor 1 antibody; NIF-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 Zinc finger protein 335 protein (672-909AA)
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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,ZNF335 Antibody (CSB-PA026683LA01HU),的标记方式是Non-conjugated。对于ZNF335 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
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推荐稀释比:
Application Recommended Dilution WB 1:500-1:5000 -
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:Component or associated component of some histone methyltransferase complexes may regulate transcription through recruitment of those complexes on gene promoters. Enhances ligand-dependent transcriptional activation by nuclear hormone receptors. Plays an important role in neural progenitor cell proliferation and self-renewal through the regulation of specific genes involved brain development, including REST. Also controls the expression of genes involved in somatic development and regulates, for instance, lymphoblast proliferation.
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基因功能参考文献:
- ZNF335 gene mutation is associated with extreme microcephaly with a severely simplified gyral pattern, decreased brain size, increased extra-axial space, enlarged ventricles, absence of the corpus callosum and delayed myelination PMID: 26479514
- In this article, we describe another family harboring ZNF335 mutations. The mutations were individually transmitted by her parents, indicating that the proband was compound heterozygous for the mutations. We speculate that invisible basal ganglia may be the key feature of ZNF335 mutations. PMID: 27540107
- we performed a meta-analysis of our data with the previous reports, identifying two further loci harbouring the ZNF335 and NIFA genes which now exceed genome-wide significance, taking the total number of CD susceptibility loci to 42. PMID: 25920553
- NIF-1 expression is associated with tumor grade in bladder cancer. PMID: 23924207
- Study identifies and characterizes a nuclear zinc finger protein, ZNF335/NIF-1, as a causative gene for severe microcephaly, small somatic size, and neonatal death. PMID: 23178126
- NRC-interacting factor 1 is a novel cotransducer that interacts with and regulates the activity of the nuclear hormone receptor coactivator NRC PMID: 12215545
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相关疾病:Microcephaly 10, primary, autosomal recessive (MCPH10)
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亚细胞定位:Nucleus.
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蛋白家族:Krueppel C2H2-type zinc-finger protein family
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组织特异性:Ubiquitously expressed.
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数据库链接:
HGNC: 15807
OMIM: 610827
KEGG: hsa:63925
STRING: 9606.ENSP00000325326
UniGene: Hs.174193
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