SAMD9L Antibody
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中文名称:SAMD9L兔多克隆抗体
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货号:CSB-PA095524
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规格:¥1100
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图片:
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The image on the left is immunohistochemistry of paraffin-embedded Human liver cancer tissue using CSB-PA095524(SAMD9L Antibody) at dilution 1/30, on the right is treated with synthetic peptide. (Original magnification: ×200)
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The image on the left is immunohistochemistry of paraffin-embedded Human brain tissue using CSB-PA095524(SAMD9L Antibody) at dilution 1/30, on the right is treated with synthetic peptide. (Original magnification: ×200)
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其他:
产品详情
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Uniprot No.:Q8IVG5
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基因名:SAMD9L
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别名:SAMD9L antibody; C7orf6 antibody; DRIF2 antibody; KIAA2005 antibody; UEF antibody; Sterile alpha motif domain-containing protein 9-like antibody; SAM domain-containing protein 9-like antibody
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宿主:Rabbit
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反应种属:Human
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免疫原:Synthetic peptide of Human SAMD9L
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免疫原种属:Homo sapiens (Human)
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标记方式:Non-conjugated
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抗体亚型:IgG
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纯化方式:Antigen affinity purification
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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:-20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol
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产品提供形式:Liquid
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应用范围:ELISA,IHC
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推荐稀释比:
Application Recommended Dilution ELISA 1:1000-1:2000 IHC 1:25-1:100 -
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:May be involved in endosome fusion. Mediates down-regulation of growth factor signaling via internalization of growth factor receptors.
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基因功能参考文献:
- Gain-of-function SAMD9L mutations cause a syndrome of cytopenia, immunodeficiency, MDS, and neurological symptoms in two unrelated Caucasian families. PMID: 28202457
- Missense Mutations in SAMD9L gene is Associated with Ataxia-Pancytopenia Syndrome. PMID: 27259050
- The findings highlight a novel tumor-suppressive role of SAMD9L inactivation by somatic mutation and decreased expression in human HBV-related HCC PMID: 25076857
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相关疾病:Ataxia-pancytopenia syndrome (ATXPC)
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亚细胞定位:Early endosome.
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组织特异性:Widely expressed in adult and fetal tissues. Variable expression in tumors. Down-regulated in breast cancer.
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数据库链接:
HGNC: 1349
OMIM: 159550
KEGG: hsa:219285
STRING: 9606.ENSP00000326247
UniGene: Hs.489118
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