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PLOD1 抗体
PLOD1
适用: 人, 小鼠
IF
宿主: 兔
Polyclonal
unconjugated
PLOD1抗体详情
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抗原
See all PLOD1 抗体
PLOD1
(Procollagen-Lysine,2-Oxoglutarate 5-Dioxygenase 1 (PLOD1))
适用
人, 小鼠
宿主
All hosts for PLOD1 抗体
兔
克隆类型
All clonalities for PLOD1 抗体
多克隆
标记
All conjugates for PLOD1 抗体
This PLOD1 antibody is un-conjugated
应用范围
All applications for PLOD1 抗体
Immunofluorescence (IF)
产品特性
Polyclonal Antibody
纯化方法
Affinity purification
免疫原
Recombinant fusion protein of human PLOD1 (NP_000293.2).
亚型
IgG
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Discover our top product PLOD1 Primary Antibody
Alternatives
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使用细节
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应用备注
IF 1:50-1:200
限制
仅限研究用
贮存及处理
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状态
Liquid
浓度
1 mg/mL
缓冲液
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.
PLOD1目标详情
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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
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.
基因ID
5351
UniProt
Q02809
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