MAB21L1 Antibody
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货号:CSB-PA623800LA01HU
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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: MAB21L1 antibody at 6µg/ml
Lane 1: A375 whole cell lysate
Lane 2: CEM whole cell lysate
Secondary
Goat polyclonal to rabbit IgG at 1/10000 dilution
Predicted band size: 41 kDa
Observed band size: 41 kDa -
Immunohistochemistry of paraffin-embedded human skeletal muscle tissue using CSB-PA623800LA01HU 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) MAB21L1 Polyclonal antibody
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Uniprot No.:Q13394
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基因名:MAB21L1
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别名:MAB21L1 antibody; CAGR1 antibody; Nbla00126Putative nucleotidyltransferase MAB21L1 antibody; EC 2.7.7.- antibody; Protein mab-21-like 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 Putative nucleotidyltransferase MAB21L1 protein (1-359AA)
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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,MAB21L1 Antibody (CSB-PA623800LA01HU),的标记方式是Non-conjugated。对于MAB21L1 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
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推荐稀释比:
Application Recommended Dilution WB 1:1000-1:5000 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.
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靶点详情
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功能:Putative nucleotidyltransferase required for several aspects of embryonic development including normal development of the eye. It is unclear whether it displays nucleotidyltransferase activity in vivo. Binds single-stranded RNA (ssRNA).
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基因功能参考文献:
- Mab21l1-/- osteoblasts also expressed higher levels of adipocyte genes and interferon-regulated genes at early stages of osteogenesis PMID: 29156428
- offer a structure-based explanation for the effects of MAB21L2 mutations in patients with eye malformations PMID: 27271801
- mab21 gene family members, mab21l1 and mab21l2, play important roles in regulating eye development. [review] PMID: 27558071
- We hypothesize that MAB21L1 haploinsufficiency cause a previously undescribed syndrome with scrotal agenesis, ophthalmological anomalies, facial dysmorphism and gross psychomotor delay as remarkable hallmarks. PMID: 27103078
- MEF is involved in PTH suppression of osteoblasts through activating the MKK4/JNK1 pathway and subsequently up-regulating Mab21l1 expression. PMID: 21465527
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亚细胞定位:Nucleus.
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蛋白家族:Mab-21 family
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组织特异性:Expressed in brain, cerebellum and skeletal muscle.
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数据库链接:
HGNC: 6757
OMIM: 601280
KEGG: hsa:4081
STRING: 9606.ENSP00000369251
UniGene: Hs.584776
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