| 產(chǎn)品編號(hào) | bsm-51372M | 
| 英文名稱 | FGFR1OP2 Mouse mAb | 
| 中文名稱 | FGFR1癌基因伴侶蛋白2單克隆抗體 | 
| 別 名 | DKFZp564O1863; FGFR1 oncogene partner 2; HSPC123; HSPC123 like; FGOP2_HUMAN. | 
| 研究領(lǐng)域 | 腫瘤 細(xì)胞生物 免疫學(xué) 信號(hào)轉(zhuǎn)導(dǎo) 生長(zhǎng)因子和激素 激酶和磷酸酶 | 
| 抗體來(lái)源 | Mouse | 
| 克隆類型 | Monoclonal | 
| 克 隆 號(hào) | 11B8 | 
| 交叉反應(yīng) | Human,Mouse,Rat | 
| 產(chǎn)品應(yīng)用 | WB=1:500-2000,ELISA=1:5000-10000
 not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.  | 
| 理論分子量 | 29 kDa | 
| 檢測(cè)分子量 | |
| 細(xì)胞定位 | 細(xì)胞漿 | 
| 性 狀 | Liquid | 
| 濃 度 | 1mg/ml | 
| 免 疫 原 | KLH conjugated synthetic peptide derived from human FGFR1OP2 | 
| 亞 型 | IgG2a | 
| 純化方法 | affinity purified by Protein G | 
| 緩 沖 液 | 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol. | 
| 保存條件 | Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles. | 
| 注意事項(xiàng) | This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. | 
| PubMed | PubMed | 
| 產(chǎn)品介紹 | 
FGFR1OP2 belongs to the SIKE family. The FGFR1OP2 (FGFR1 oncogene partner 2) gene was identified through its involvement in a fusion with the FGFR1 gene. FGFR1OP2 may be involved in the wound healing pathway. It is expressed in bone marrow, spleen and thymus. A chromosomal aberration involving FGFR1OP2 may be a cause of stem cell myeloproliferative disorder (MPD). Insertion ins(12;8)(p11;p11p22) with FGFR1. MPD is characterized by myeloid hyperplasia, eosinophilia and T cell or B cell lymphoblastic lymphoma. In general it progresses to acute myeloid leukemia. The fusion protein FGFR1OP2-FGFR1 may exhibit constitutive kinase activity and be responsible for the transforming activity. Function: May be involved in wound healing pathway (By similarity). Subcellular Location: Cytoplasm (By similarity). Tissue Specificity: Expressed in bone marrow, spleen and thymus. DISEASE: Note=A chromosomal aberration involving FGFR1OP2 may be a cause of stem cell myeloproliferative disorder (MPD). Insertion ins(12;8)(p11;p11p22) with FGFR1. MPD is characterized by myeloid hyperplasia, eosinophilia and T-cell or B-cell lymphoblastic lymphoma. In general it progresses to acute myeloid leukemia. The fusion protein FGFR1OP2-FGFR1 may exhibit constitutive kinase activity and be responsible for the transforming activity. Similarity: Belongs to the SIKE family. SWISS: Q9NVK5 Gene ID: 26127 Database links: Entrez Gene: 26127 Human Entrez Gene: 67529 Mouse Omim: 608858 Human SwissProt: Q9NVK5 Human SwissProt: Q9CRA9 Mouse Unigene: 591162 Human Unigene: 333499 Mouse Unigene: 68658 Rat  |