XK Antibody
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货号:CSB-PA908755
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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-PA908755(XK Antibody) at dilution 1/20, 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 esophagus cancer tissue using CSB-PA908755(XK Antibody) at dilution 1/20, on the right is treated with synthetic peptide. (Original magnification: ×200)
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Gel: 8%SDS-PAGE, Lysate: 40 μg, Lane 1-2: Human normal liver and placenta tissue, Primary antibody: CSB-PA908755(XK Antibody) at dilution 1/350 dilution, Secondary antibody: Goat anti rabbit IgG at 1/8000 dilution, Exposure time: 2 minutes
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其他:
产品详情
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Uniprot No.:P51811
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基因名:XK
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别名:XK antibody; XKR1 antibody; XRG1 antibody; Membrane transport protein XK antibody; Kell complex 37 kDa component antibody; Kx antigen antibody; XK-related protein 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:Synthetic peptide of Human XK
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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,WB,IHC
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推荐稀释比:
Application Recommended Dilution ELISA 1:2000-1:5000 WB 1:500-1:2000 IHC 1:20-1:100 -
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.
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靶点详情
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功能:May be involved in sodium-dependent transport of neutral amino acids or oligopeptides.
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基因功能参考文献:
- the expression of KX is critical to normal morphology, and null mutations are associated with the McLeod neuroacanthocytosis syndrome. PMID: 26308465
- The XK gene was not linked to hypermutability in red cells from patients with paroxysmal nocturnal hemoglobinuria. PMID: 24816235
- study reports the clinical findings and a novel nonsense hemizygous mutation, c.154C>T (p.Gln52X) at exon 1 of XK gene in a Taiwanese family with McLeod syndrome PMID: 24635891
- Novel XK protein mutations are reported in two patients who exhibit typical clinical characteristics of McLeod syndrome. PMID: 21463873
- This study identified one non-synonymous and one intron variant in mood disorder and schizophrenia subjects, respectively, in XK. PMID: 21145924
- In human cortex, the results show expression of XK in cortical neurons with an apparent cytoplasmic localization. PMID: 17379193
- Sequence analysis demonstrated a 5 bp deletion in exon 2 of the XK gene in McLeod syndrome. PMID: 17469188
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相关疾病:McLeod syndrome (MLS)
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亚细胞定位:Cell membrane; Multi-pass membrane protein.
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蛋白家族:XK family
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组织特异性:High levels in skeletal muscle, heart, brain, and pancreas; low levels in placenta, lung, liver, and kidney.
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数据库链接:
HGNC: 12811
OMIM: 300842
KEGG: hsa:7504
STRING: 9606.ENSP00000367879
UniGene: Hs.78919
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