ROGDI Antibody
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货号:CSB-PA867108LA01HU
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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: ROGDI antibody at 1.2µg/ml
Lane 1: Hela whole cell lysate
Lane 2: K562 whole cell lysate
Secondary
Goat polyclonal to rabbit IgG at 1/10000 dilution
Predicted band size: 33 kDa
Observed band size: 33 kDa -
Immunohistochemistry of paraffin-embedded human kidney tissue using CSB-PA867108LA01HU at dilution of 1:100
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Immunohistochemistry of paraffin-embedded human pancreatic tissue using CSB-PA867108LA01HU 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) ROGDI Polyclonal antibody
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Uniprot No.:Q9GZN7
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基因名:ROGDI
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别名:FLJ22386 antibody; KTZS antibody; Leucine zipper domain protein antibody; Protein rogdi homolog antibody; rogdi antibody; rogdi homolog (Drosophila) antibody; rogdi, Drosophila, homolog of antibody; ROGDI_HUMAN 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 Protein rogdi homolog protein (14-287AA)
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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,ROGDI Antibody (CSB-PA867108LA01HU),的标记方式是Non-conjugated。对于ROGDI 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:Antigen Affinity 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
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推荐稀释比:
Application Recommended Dilution WB 1:500-1:2000 IHC 1:20-1:200 -
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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基因功能参考文献:
- We identify novel compound heterozygous ROGDI mutations in five typical Kohlschutter-Tonz syndrome families. Other families were negative for ROGDI mutations, suggesting genetic heterogeneity of atypical forms of the disease. PMID: 23086778
- The finding that ROGDI mutations cause Kohlschutter-Tonz Syndrome indicates that the protein product of this gene plays an important role in neuronal development as well as amelogenesis. PMID: 22424600
- Homozygosity mapping localized the gene linked to Kohlschutter-Tonz syndrome to a 586,513 bp region (with a LOD score of 6.4) in chromosomal region 16p13.3. The nonsense mutation was homozygous in all affected individuals. PMID: 22482807
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相关疾病:Kohlschuetter-Toenz syndrome (KTZS)
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亚细胞定位:Nucleus envelope. Cell junction, synapse, presynapse. Cell projection, axon. Perikaryon. Cell projection, dendrite. Cytoplasmic vesicle, secretory vesicle, synaptic vesicle.
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蛋白家族:Rogdi family
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组织特异性:Widely expressed with highest levels in spinal cord, brain, heart and bone marrow. Also expressed in fetal brain and liver.
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数据库链接:
HGNC: 29478
OMIM: 226750
KEGG: hsa:79641
UniGene: Hs.459795
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