-
- 抗原 See all ROR2 抗体
- ROR2 (Receptor Tyrosine Kinase-Like Orphan Receptor 2 (ROR2))
-
抗原表位
- AA 100-200
-
适用
- 人
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This ROR2 antibody is un-conjugated
-
应用范围
- Western Blotting (WB), Immunohistochemistry (IHC)
- 序列
- APVVQEPRRI IIRKTEYGSR LRIQDLDTTD TGYYQCVATN GMKTITATGV LFVRLGPTHS PNHNFQDDYH EDGFCQPYRG IACARFIGNR TIYVDSLQMQ G
- 交叉反应
- 人, 小鼠, 大鼠
- 产品特性
- Polyclonal Antibodies
- 免疫原
- A synthetic peptide corresponding to a sequence within amino acids 100-200 of human ROR2 (NP_004551.2).
- 亚型
- IgG
- Top Product
- Discover our top product ROR2 Primary Antibody
-
-
- 应用备注
- WB,1:500 - 1:2000,IHC,1:100 - 1:200
- 说明
-
HIGH QUALITY
- 限制
- 仅限研究用
-
- 状态
- Liquid
- 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.
-
-
Wnt5a mediated canonical Wnt signaling pathway activation in orthodontic tooth movement: possible role in the tension force-induced bone formation." in: Journal of molecular histology, Vol. 47, Issue 5, pp. 455-66, (2017) (PubMed).
: "
-
Wnt5a mediated canonical Wnt signaling pathway activation in orthodontic tooth movement: possible role in the tension force-induced bone formation." in: Journal of molecular histology, Vol. 47, Issue 5, pp. 455-66, (2017) (PubMed).
-
- 抗原
- ROR2 (Receptor Tyrosine Kinase-Like Orphan Receptor 2 (ROR2))
- 别名
- ROR2 (ROR2 产品)
- 背景
- The protein encoded by this gene is a receptor protein tyrosine kinase and type I transmembrane protein that belongs to the ROR subfamily of cell surface receptors. The protein may be involved in the early formation of the chondrocytes and may be required for cartilage and growth plate development. Mutations in this gene can cause brachydactyly type B, a skeletal disorder characterized by hypoplasia/aplasia of distal phalanges and nails. In addition, mutations in this gene can cause the autosomal recessive form of Robinow syndrome, which is characterized by skeletal dysplasia with generalized limb bone shortening, segmental defects of the spine, brachydactyly, and a dysmorphic facial appearance.,ROR2,BDB,BDB1,NTRKR2,Signal Transduction,Kinase,Tyrosine kinases,Cell Biology & Developmental Biology,Cytoskeleton,Extracellular Matrix,Bone,Stem Cells,Mesenchymal Stem Cells,ROR2
- 分子量
- 104 kDa
- 基因ID
- 4920
- UniProt
- Q01974
- 途径
- RTK signaling, WNT signaling
-