免费的东京热一区二区三区,亚洲男人的天堂2022在线,国产精品8页第64页,伊香蕉网站在线观看香蕉,美女主播大秀免费视频,久久一区二区三区四区高清无

亚洲国产日韩不卡综合,明星ai换脸磁力资源种子搜索,成人性闻CCAV下载,欧美日本国产在线a小说v,亚洲欧洲综合一区二区三区,里中结衣av中文字幕

> > > >

PLOD1 rabbit pAb

商品貨號(hào)： PLA020911

適應(yīng) 性： 人,小鼠,大鼠

￥600元

規(guī)格：

40μL 100μL 200μL

在線咨詢

MSDS

說明書

商品描述

基因名稱： PLOD1 LLH PLOD
蛋白名稱： PLOD1
Human_gene_id： 5351
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=5351
Human_swiss_prot_no： Q02809
Human_swiss_link： https://www.uniprot.org/uniprotkb/Q02809/entry
Mouse_gene_id： 18822
Mouse_gene_link： https://www.uniprot.org/uniprot/18822
Mouse_swiss_prot_no： Q9R0E2
Mouse_swiss_link： https://www.uniprot.org/uniprotkb/Q9R0E2
Rat_swiss_prot_no： Q63321
Rat_swiss_link： https://www.uniprot.org/uniprotkb/Q63321
特異性： This antibody detects endogenous levels of PLOD1 at Human/Mouse/Rat
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;IHC-p 1:50-300; ELISA 2000-20000
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(chǔ)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： 80kD
功能： catalytic activity:Procollagen L-lysine + 2-oxoglutarate + O(2) = procollagen 5-hydroxy-L-lysine + succinate + CO(2).,cofactor:Ascorbate.,cofactor:Iron.,disease:Defects in PLOD1 are the cause of Ehlers-Danlos syndrome type 6 (EDS6) [MIM:225400]. EDS is a connective tissue disorder characterized by hyperextensible skin, atrophic cutaneous scars due to tissue fragility and joint hyperlaxity. EDS6 is characterized by the presence of ocular complications, particularly retinal detachment.,disease:Defects in PLOD1 are the cause of Nevo syndrome [MIM:601451]. This is a rare, autosomal recessive disorder characterized by increased perinatal length, kyphosis, muscular hypotonia, and joint laxity. Nevo syndrome and EDS-VI have similar clinical phenotypes. Some authors consider that both syndromes are the same clinical entity.,function:Forms hydroxylysine residues in -Xaa-Lys-Gly- sequences in collagens. These hydroxylysines serve as sites of attachment for carbohydrate units and are essential for the stability of the intermolecular collagen cross-links.,similarity:Contains 1 PKHD (prolyl/lysyl hydroxylase) domain.,subunit:Homodimer.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細(xì)胞定位： Rough endoplasmic reticulum membrane; Peripheral membrane protein; Lumenal side.
科研貨號(hào)： PLA020911

PLOD1 rabbit pAb

Catalog No PLA020911

Product information

基因名稱： PLOD1 LLH PLOD
蛋白名稱： PLOD1
Human_gene_id： 5351
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=5351
Human_swiss_prot_no： Q02809
Human_swiss_link： https://www.uniprot.org/uniprotkb/Q02809/entry
Mouse_gene_id： 18822
Mouse_gene_link： https://www.uniprot.org/uniprot/18822
Mouse_swiss_prot_no： Q9R0E2
Mouse_swiss_link： https://www.uniprot.org/uniprotkb/Q9R0E2
Rat_swiss_prot_no： Q63321
Rat_swiss_link： https://www.uniprot.org/uniprotkb/Q63321
特異性： This antibody detects endogenous levels of PLOD1 at Human/Mouse/Rat
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;IHC-p 1:50-300; ELISA 2000-20000
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(chǔ)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： 80kD
功能： catalytic activity:Procollagen L-lysine + 2-oxoglutarate + O(2) = procollagen 5-hydroxy-L-lysine + succinate + CO(2).,cofactor:Ascorbate.,cofactor:Iron.,disease:Defects in PLOD1 are the cause of Ehlers-Danlos syndrome type 6 (EDS6) [MIM:225400]. EDS is a connective tissue disorder characterized by hyperextensible skin, atrophic cutaneous scars due to tissue fragility and joint hyperlaxity. EDS6 is characterized by the presence of ocular complications, particularly retinal detachment.,disease:Defects in PLOD1 are the cause of Nevo syndrome [MIM:601451]. This is a rare, autosomal recessive disorder characterized by increased perinatal length, kyphosis, muscular hypotonia, and joint laxity. Nevo syndrome and EDS-VI have similar clinical phenotypes. Some authors consider that both syndromes are the same clinical entity.,function:Forms hydroxylysine residues in -Xaa-Lys-Gly- sequences in collagens. These hydroxylysines serve as sites of attachment for carbohydrate units and are essential for the stability of the intermolecular collagen cross-links.,similarity:Contains 1 PKHD (prolyl/lysyl hydroxylase) domain.,subunit:Homodimer.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細(xì)胞定位： Rough endoplasmic reticulum membrane; Peripheral membrane protein; Lumenal side.
科研貨號(hào)： PLA020911

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.

亚洲国产日韩不卡综合,明星ai换脸磁力资源种子搜索,成人性闻CCAV下载,欧美日本国产在线a小说v,亚洲欧洲综合一区二区三区,里中结衣av中文字幕