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MAN1 rabbit pAb

商品貨號： PLA020862

適應(yīng) 性： 人,小鼠

￥600元

規(guī)格：

40μL 100μL 200μL

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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(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細(xì)胞定位： Nucleus inner membrane ; Multi-pass membrane protein .
組織表達(dá)： 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(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細(xì)胞定位： Nucleus inner membrane ; Multi-pass membrane protein .
組織表達(dá)： Heart, brain, placenta, lung, liver and skeletal muscle.
科研貨號： PLA020862

Hunan UPT Biotechnology Co.,Ltd

Website：m.tjdqdt.com Servive hotline :4006916686

E-mail：service@uptbio.com

Address：

Room 402, Building 13, Xinggong International Industrial Park, 100 Guyuan Road, Yuelu District, Changsha City, Hunan Province, China.

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