- 询价
- XY-Bioscience
- 中国/美国/德国
- XYF494Ra01
- 2025年07月09日
- WB, ICC, IHC-P, IHC-F, ELISA
- Rabbit，兔
- 见说明书
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
见说明书
- 亚型：
见说明书
- 形态：
液态/粉末
- 保存条件：
-20oC
- 克隆性：
多克隆
- 标记物：
未标记
- 适应物种：
见说明书
- 宿主：
Rabbit，兔
- 应用范围：
WB, ICC, IHC-P, IHC-F, ELISA
- 浓度：
200ug/ml
- 靶点：
见说明书
- 抗体英文名：
Polyclonal Antibody to Janus Kinase 2 (JAK2)
- 抗体名：
Janus激酶2(JAK2)多克隆抗体
| Organism species | Rattus norvegicus (Rat) |
| Product No. | XYF494Ra01 |
| Clonality | Polyclonal |
| Host | Rabbit |
| Immunoglobulin Type | IgG |
| Purification | Affinity Chromatography |
| Applications | WB, ICC, IHC-P, IHC-F, ELISA |
| Concentration | 200ug/ml |
| UOM | 100ug |
| Conjugate | No Conjugate |
Immunocytochemistry in formalin fixed cells: 1:50-500
Immunohistochemistry in formalin fixed frozen section: 1:50-500
Immunohistochemistry in paraffin section: 1:10-100
Enzyme-linked Immunosorbent Assay: 1:100-1:5000
Optimal working dilutions must be determined by end user.
containing 0.02% NaN3, 50% glycerol.
Usage: 10uL per well when 3,3'-Diaminobenzidine(DAB) as the substrate.
5uL per well when used in enhanced chemilumescent (ECL).
Note: The quality control is specifically manufactured as the positive control. Not used for other purposes.
Loading Buffer: 100mM Tris(pH8.8), 2% SDS, 200mM NaCl, 50% glycerol, BPB 0.01%, NaN3 0.02%.
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文献和实验受体相关性蛋白酪氨酸激酶介导的信号途径 大部分细胞因子受体分子胞内区不带有启动信号转导的蛋白酪氨酸激酶(PTK)结构域，但可通过相应胞内区连接的PTK起作用。CkR―F和IFNR―F的受体分子胞内区都结合有PTK中的Janus激酶(Janus kinase，Jak)家族成员，包括Jakl、Jak2、Jak3和Tyk2。细胞因子各种受体的亚单位往往连接Jak家族中的一个或几个特定成员。如C―CSFR与Jak2连接，IL2Rβ链与Jakl、IL2Rγ链与Jak3连接，ILl0R
Immunoprecipitation to Determine JAK Kinase Activation in Response to Interleukins in Ovarian Cancer
In cytokine receptors, there is no consensus sequence motif for tyrosine and/or serine/threonine kinases in its intracellular domain (1 ). Cytokine receptors associate with and activate members of the Janus kinase family (JAK
of NFκB, p38 and JNK, as well as Myd88-dependent activation of ERK. JAK2 has also been shown to be involved in NFκB activation. Crosstalk of IL-33 with c-kit signaling has been proposed to enhance the activation of ERK, JNK, PKB and STAT3 in mast cells
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