Adamts2 抗体
-
- 抗原 See all Adamts2 抗体
- Adamts2 (ADAM Metallopeptidase with Thrombospondin Type 1 Motif, 2 (Adamts2))
-
适用
- 人, 小鼠, 大鼠
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This Adamts2 antibody is un-conjugated
-
应用范围
- Western Blotting (WB)
- 产品特性
- Polyclonal Antibody
- 纯化方法
- Affinity purification
- 免疫原
- Recombinant protein of mouse ADAMTS2
- 亚型
- IgG
- Top Product
- Discover our top product Adamts2 Primary Antibody
-
-
- 应用备注
- WB 1:500-1:2000
- 限制
- 仅限研究用
-
- 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.
-
- 抗原
- Adamts2 (ADAM Metallopeptidase with Thrombospondin Type 1 Motif, 2 (Adamts2))
- 别名
- ADAMTS2 (Adamts2 产品)
- 别名
- ADAM-TS2 antibody, ADAMTS-2 antibody, ADAMTS-3 antibody, PCINP antibody, hPCPNI antibody, mKIAA4060 antibody, pNPI antibody, NPI antibody, PC I-NP antibody, PCI-NP antibody, PCPNI antibody, PNPI antibody, RGD1565950 antibody, a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 2 antibody, ADAM metallopeptidase with thrombospondin type 1 motif 2 antibody, ADAM metallopeptidase with thrombospondin type 1 motif, 2 antibody, Adamts2 antibody, ADAMTS2 antibody
- 背景
- This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The encoded preproprotein is proteolytically processed to generate the mature procollagen N-proteinase. This proteinase excises the N-propeptide of the fibrillar procollagens types I-III and type V. Mutations in this gene cause Ehlers-Danlos syndrome type VIIC, a recessively inherited connective-tissue disorder. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed.
- 分子量
-
Observed_MW: 120 kDa
Calculated_MW: 61 kDa/134 kDa
- 基因ID
- 216725
- UniProt
- Q8C9W3
-