LAMC3 Antibody
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货号:CSB-PA012737GA01HU
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规格:¥3,900
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其他:
产品详情
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Uniprot No.:Q9Y6N6
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基因名:
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别名:LAMA 1 antibody; LAMA antibody; LAMA1 antibody; LAMB1 antibody; Lamc3 antibody; LAMC3_HUMAN antibody; Laminin A chain antibody; Laminin alpha 1 antibody; Laminin alpha 1 chain antibody; Laminin B1 chain antibody; Laminin subunit beta 1 antibody; Laminin subunit gamma-3 antibody; Laminin-12 subunit gamma antibody; Laminin-14 subunit gamma antibody; Laminin-15 subunit gamma antibody
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宿主:Rabbit
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反应种属:Human
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免疫原:Human LAMC3-Specific
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免疫原种属:Homo sapiens (Human)
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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:PBS with 0.02% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
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产品提供形式:Liquid
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应用范围:ELISA,WB
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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:Binding to cells via a high affinity receptor, laminin is thought to mediate the attachment, migration and organization of cells into tissues during embryonic development by interacting with other extracellular matrix components.
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基因功能参考文献:
- LAMC3 gene variation is associated with oral cavity and pharyngeal cancer. PMID: 27749845
- We found statistically significant association with AAO for three genes (WRN, NTN4 and LAMC3) with common associated variants. PMID: 26394601
- These data suggest that beta2 and gamma3-containing laminins play an important dose-dependent role in development of the cortical pial basement membrane PMID: 22961762
- Recessive LAMC3 mutations cause malformations of occipital cortical development. PMID: 21572413
- Laminin isoforms containing the gamma3 chain are unable to bind to integrins due to the absence of the glutamic acid residue conserved in the C-terminal regions of the gamma1 and gamma2 chains PMID: 18697739
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相关疾病:Cortical malformations occipital (OCCM)
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亚细胞定位:Secreted, extracellular space, extracellular matrix, basement membrane.
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组织特异性:Broadly expressed in: skin, heart, lung, and the reproductive tracts.
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数据库链接:
HGNC: 6494
OMIM: 604349
KEGG: hsa:10319
STRING: 9606.ENSP00000354360
UniGene: Hs.201805
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