PLOD1 抗体
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- 抗原 See all PLOD1 抗体
- PLOD1 (Procollagen-Lysine,2-Oxoglutarate 5-Dioxygenase 1 (PLOD1))
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适用
- 小鼠
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This PLOD1 antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 纯化方法
- Affinity purification
- 免疫原
- Recombinant protein of human PLOD1
- 亚型
- IgG
- Top Product
- Discover our top product PLOD1 Primary Antibody
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- 应用备注
- WB 1:500 - 1:2000
- 限制
- 仅限研究用
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- 浓度
- 1 mg/mL
- 缓冲液
- Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3.
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- 抗原
- PLOD1 (Procollagen-Lysine,2-Oxoglutarate 5-Dioxygenase 1 (PLOD1))
- 别名
- PLOD1 (PLOD1 产品)
- 别名
- EDS6 antibody, LH antibody, LH1 antibody, LLH antibody, PLOD antibody, Plod antibody, procollagen-lysine antibody, 2410042F05Rik antibody, AI854890 antibody, AV007929 antibody, Lh1 antibody, plod1 antibody, ik:tdsubs_rzpd609-29b19 antibody, plod antibody, wu:fc29c10 antibody, wu:fc95g08 antibody, wu:fi18a05 antibody, zgc:152876 antibody, procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 antibody, procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1 antibody, procollagen-lysine,2-oxoglutarate 5-dioxygenase 3 antibody, procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1 L homeolog antibody, procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1a antibody, PLOD1 antibody, Plod1 antibody, PLOD3 antibody, plod1.L antibody, plod1a antibody
- 背景
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Synonyms: 2-oxoglutarate 5-dioxygenase 1,EDS6,LH,LH1,LLH,Lysine hydroxylase,Lysyl hydroxylase 1,PLOD,Plod1,PLOD1,Procollagen lysine 1 2 oxoglutarate 5 dioxygenase 1,Procollagen lysine 2 oxoglutarate 5 dioxygenase 1,Procollagen-lysine
Background: Lysyl hydroxylase is a membrane-bound homodimeric protein localized to the cisternae of the endoplasmic reticulum. The enzyme (cofactors iron and ascorbate) catalyzes the hydroxylation of lysyl residues in collagen-like peptides. The resultant hydroxylysyl groups are attachment sites for carbohydrates in collagen and thus are critical for the stability of intermolecular crosslinks. Some patients with Ehlers-Danlos syndrome type VI have deficiencies in lysyl hydroxylase activity. Two transcript variants encoding different isoforms have been found for this gene.
- 分子量
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Observed_MW: Refer to figures
Calculated_MW: 83kDa/88kDa
- 基因ID
- 5351
- UniProt
- Q02809
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