MGP 抗体
Our Local Distributor
北京 101111
Quick Overview for MGP 抗体 (ABIN7246430)
抗原
See all MGP 抗体适用
宿主
克隆类型
标记
应用范围
-
-
产品特性
- Polyclonal Antibody
-
纯化方法
- Antigen affinity purification
-
免疫原
- Fusion protein of human MGP
-
亚型
- IgG
-
-
anti-Matrix Gla Protein (MGP) (AA 20-103) antibody
MGP 适用: 人 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Matrix Gla Protein (MGP) antibodyMGP 适用: 人, 大鼠, 小鼠 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Matrix Gla Protein (MGP) (AA 20-96) antibodyMGP 适用: 人 IHC, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Matrix Gla Protein (MGP) (AA 37-66) antibodyMGP 适用: 人 WB, IHC (p), FACS 宿主: 兔 Polyclonal unconjugated
anti-Matrix Gla Protein (MGP) (AA 1-103) antibodyMGP 适用: 人 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Matrix Gla Protein (MGP) (AA 20-104) antibodyMGP 适用: 小鼠 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Matrix Gla Protein (MGP) (AA 20-103) antibodyMGP 适用: Cow WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Matrix Gla Protein (MGP) (AA 1-103) antibodyMGP 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Matrix Gla Protein (MGP) (AA 20-96) antibodyMGP 适用: 人 WB, IHC 宿主: 兔 Polyclonal unconjugated
-
-
应用备注
- IHC 1:70-1:350, ELISA 1:5000-1:10000
-
限制
- 仅限研究用
-
-
-
状态
- Liquid
-
浓度
- 1.32 mg/mL
-
缓冲液
- PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
-
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.
-
-
- MGP (Matrix Gla Protein (MGP))
-
别名
- MGP
-
背景
- Matrix Gla protein (MGP) is is a vitamin K-dependent,extracellular matrix protein. MGP plays a pivotal role in preventing soft tissue calcification and local mineralization of the vascular wall. Vitamin K deficiency leads to inactive uncarboxylated MGP (ucMGP),which accumulates at sites of arterial calcification. However MGP is synthesized in many tissues and is especially enriched in embryonic tissues and in cancer cells. Defects in MGP are the cause of Keutel syndrome (KS),which is an autosomal recessive disorder characterized by abnormal cartilage calcification,peripheral pulmonary stenosis neural hearing loss and midfacial hypoplasia.
-
UniProt
- P08493
抗原
-
