货号
产品规格
售价
备注
BN40236R-100ul
100ul
¥2360.00
交叉反应:Human,Mouse,Rat 推荐应用:WB,IHC-P,IHC-F,IF,ELISA
BN40236R-200ul
200ul
¥3490.00
交叉反应:Human,Mouse,Rat 推荐应用:WB,IHC-P,IHC-F,IF,ELISA
产品描述
英文名称 | PTOV1 |
中文名称 | 前列腺肿瘤高表达蛋白1抗体 |
别 名 | ACID2; Activator interaction domain containing protein 2; Gcap3; prostate tumor overexpressed 1; Prostate tumor overexpressed gene 1; PTOV 1; PTOV1_HUMAN; Prostate tumor-overexpressed gene 1 protein; PTOV-1; Activator interaction domain-containing protein 2. |
研究领域 | 肿瘤 免疫学 染色质和核信号 转录调节因子 |
抗体来源 | Rabbit |
克隆类型 | Polyclonal |
交叉反应 | Human, Mouse, Rat, |
产品应用 | WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:100-500 (石蜡切片需做抗原修复) not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
分 子 量 | 47kDa |
细胞定位 | 细胞核 细胞膜 |
性 状 | Liquid |
浓 度 | 1mg/ml |
免 疫 原 | KLH conjugated synthetic peptide derived from human PTOV1:61-160/416 |
亚 型 | IgG |
纯化方法 | affinity purified by Protein A |
储 存 液 | 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. |
保存条件 | Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. |
PubMed | PubMed |
产品介绍 | PTOV1 belongs to the Mediator complex subunit 25 family, PTOV1 subfamily. It may activate transcription and is required for nuclear translocation of FLOT1. PTOV1 promotes cell proliferation. There are three named isoforms. Function: PTH elevates calcium level by dissolving the salts in bone and preventing their renal excretion. Stimulates [1-14C]-2-deoxy-D-glucose (2DG) transport and glycogen synthesis in osteoblastic cells. Subunit: Interacts with PTH1R (via N-terminal extracellular domain). Subcellular Location: Secreted. DISEASE: Defects in PTH are a cause of familial isolated hypoparathyroidism (FIH) [MIM:146200]; also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism. Similarity: Belongs to the parathyroid hormone family. SWISS: Q86YD1 Gene ID: 53635 Database links: Entrez Gene: 53635 Human Entrez Gene: 84113 Mouse Omim: 610195 Human SwissProt: Q86YD1 Human SwissProt: Q91VU8 Mouse Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |