ROR2 Protein (Myc-DYKDDDDK Tag)
Quick Overview for ROR2 Protein (Myc-DYKDDDDK Tag) (ABIN2731087)
抗原
See all ROR2 蛋白蛋白类型
宿主
资源
应用范围
纯度
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标记
- This ROR2 protein is labelled with Myc-DYKDDDDK Tag.
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产品特性
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- Recombinant human ROR2 protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
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Receptor Tyrosine Kinase-Like Orphan Receptor 2 (ROR2) (AA 34-403) protein (His-Avi Tag)
ROR2 宿主: 人 宿主: HEK-293 Cells Recombinant > 95 % as determined by Tris-Bis PAGE,> 95 % as determined by HPLC
Receptor Tyrosine Kinase-Like Orphan Receptor 2 (ROR2) (AA 34-403) protein (Fc Tag)ROR2 宿主: 人 宿主: HEK-293 Cells Recombinant > 95 % as determined by Tris-Bis PAGE,> 95 % as determined by HPLC
Receptor Tyrosine Kinase-Like Orphan Receptor 2 (ROR2) (AA 34-403) protein (His-Avi Tag,Biotin)ROR2 宿主: 人 宿主: HEK-293 Cells Recombinant > 95 % as determined by Tris-Bis PAGE,> 95 % as determined by HPLC
Receptor Tyrosine Kinase-Like Orphan Receptor 2 (ROR2) (AA 34-403) protein (His tag)ROR2 宿主: 人 宿主: HEK-293 Cells Recombinant The purity of the protein is greater than 95 % as determined by SDS-PAGE and Coomassie blue staining.
Receptor Tyrosine Kinase-Like Orphan Receptor 2 (ROR2) (AA 34-403) protein (His tag)ROR2 宿主: 小鼠 宿主: Mammalian Cells Recombinant The purity of the protein is greater than 85 % as determined by SDS-PAGE and Coomassie blue staining.
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应用备注
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays -
说明
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The tag is located at the C-terminal.
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限制
- 仅限研究用
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浓度
- 50 μg/mL
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缓冲液
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
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储存条件
- -80 °C
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储存方法
- Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
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- ROR2 (Receptor Tyrosine Kinase-Like Orphan Receptor 2 (ROR2))
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别名
- Ror2
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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.
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分子量
- 101.3 kDa
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NCBI登录号
- NP_004551
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途径
- RTK signaling, WNT signaling
抗原
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