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MAN1 rabbit pAb
商品貨號: PLA020862
適 應 性: 人,小鼠
WB
¥600元
規格:
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MSDS
說明書
商品描述
  • 基因名稱: LEMD3 MAN1
  • 蛋白名稱: MAN1
  • Human_gene_id: 23592
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=23592
  • Human_swiss_prot_no: Q9Y2U8
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/Q9Y2U8/entry
  • Mouse_gene_id: 380664
  • Mouse_gene_link: https://www.uniprot.org/uniprot/380664
  • Mouse_swiss_prot_no: Q9WU40
  • Mouse_swiss_link: https://www.uniprot.org/uniprotkb/Q9WU40
  • 特異性: This antibody detects endogenous levels of MAN1 at Human/Mouse
  • 組成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 來源: Polyclonal, Rabbit,IgG
  • 稀釋: WB 1:500-2000
  • 純化工藝: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
  • 濃度: 1 mg/ml
  • 儲存: -15°C to -25°C/1 year(Do not lower than -25°C)
  • 說明書: 1
  • Msds: MSDS_Antibody.pdf
  • 分子量: 100kD
  • 功能: disease:Defects in LEMD3 are a cause of melorheostosis [MIM:155950]. Melorheostosis is a rare mesenchymal dysplasia and one of the sclerosing bone disorders. It is caused by a developmental error, with a sclerotomal distribution, frequently involving one limb. It may be asymptomatic, but pain, stiffness with limitation of motion, leg-length discrepancy and limb deformity may occur.,disease:Defects in LEMD3 are the cause of Buschke-Ollendorff syndrome (BOS) [MIM:166700]; also known as dermatoosteopoikilosis or disseminated dermatofibrosis with osteopoikilosis or dermatofibrosis lenticularis disseminata with osteopoikilosis or osteopathia condensans disseminata. BOS refers to the association of osteopoikilosis with disseminated connective-tissue nevi. Osteopoikilosis is a skeletal dysplasia characterized by a symmetric but unequal distribution of multiple hyperostotic areas in different parts of the skeleton. Both elastic-type nevi (juvenile elastoma) and collagen-type nevi (dermatofibrosis lenticularis disseminata) have been described in BOS. Skin or bony lesions can be absent in some family members, whereas other relatives may have both.,similarity:Contains 1 LEM domain.,tissue specificity:Heart, brain, placenta, lung, liver and skeletal muscle.,
  • 相關產品: RS0001,RS0002,YM3028,YM3029
  • 細胞定位: Nucleus inner membrane ; Multi-pass membrane protein .
  • 組織表達: Heart, brain, placenta, lung, liver and skeletal muscle.
  • 科研貨號: PLA020862
MAN1 rabbit pAb
Catalog No PLA020862
Product information
  • 基因名稱: LEMD3 MAN1
  • 蛋白名稱: MAN1
  • Human_gene_id: 23592
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=23592
  • Human_swiss_prot_no: Q9Y2U8
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/Q9Y2U8/entry
  • Mouse_gene_id: 380664
  • Mouse_gene_link: https://www.uniprot.org/uniprot/380664
  • Mouse_swiss_prot_no: Q9WU40
  • Mouse_swiss_link: https://www.uniprot.org/uniprotkb/Q9WU40
  • 特異性: This antibody detects endogenous levels of MAN1 at Human/Mouse
  • 組成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 來源: Polyclonal, Rabbit,IgG
  • 稀釋: WB 1:500-2000
  • 純化工藝: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
  • 濃度: 1 mg/ml
  • 儲存: -15°C to -25°C/1 year(Do not lower than -25°C)
  • 說明書: 1
  • Msds: MSDS_Antibody.pdf
  • 分子量: 100kD
  • 功能: disease:Defects in LEMD3 are a cause of melorheostosis [MIM:155950]. Melorheostosis is a rare mesenchymal dysplasia and one of the sclerosing bone disorders. It is caused by a developmental error, with a sclerotomal distribution, frequently involving one limb. It may be asymptomatic, but pain, stiffness with limitation of motion, leg-length discrepancy and limb deformity may occur.,disease:Defects in LEMD3 are the cause of Buschke-Ollendorff syndrome (BOS) [MIM:166700]; also known as dermatoosteopoikilosis or disseminated dermatofibrosis with osteopoikilosis or dermatofibrosis lenticularis disseminata with osteopoikilosis or osteopathia condensans disseminata. BOS refers to the association of osteopoikilosis with disseminated connective-tissue nevi. Osteopoikilosis is a skeletal dysplasia characterized by a symmetric but unequal distribution of multiple hyperostotic areas in different parts of the skeleton. Both elastic-type nevi (juvenile elastoma) and collagen-type nevi (dermatofibrosis lenticularis disseminata) have been described in BOS. Skin or bony lesions can be absent in some family members, whereas other relatives may have both.,similarity:Contains 1 LEM domain.,tissue specificity:Heart, brain, placenta, lung, liver and skeletal muscle.,
  • 相關產品: RS0001,RS0002,YM3028,YM3029
  • 細胞定位: Nucleus inner membrane ; Multi-pass membrane protein .
  • 組織表達: Heart, brain, placenta, lung, liver and skeletal muscle.
  • 科研貨號: PLA020862
  • Hunan UPT Biotechnology Co.,Ltd
    Website:www.zjgzfxx.com Servive hotline :4006916686
    E-mail:service@uptbio.com
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