货号
产品规格
售价
备注
BN41162R-100ul
100ul
¥2360.00
交叉反应:Mouse,Rat(predicted:Human,Dog,Pig) 推荐应用:WB,IHC-P,IHC-F,IF,ELISA
BN41162R-200ul
200ul
¥3490.00
交叉反应:Mouse,Rat(predicted:Human,Dog,Pig) 推荐应用:WB,IHC-P,IHC-F,IF,ELISA
产品描述
英文名称 | GIG34 |
中文名称 | 细胞生长抑制蛋白34 |
别 名 | 60S ribosomal protein L11; Cell growth inhibiting protein 34; Cell growth inhibiting protein34; CLL associated antigen KW 12; CLL associated antigen KW12; DBA 7; DBA7; GIG 34; GIG34; Ribosomal protein L11; RPL 11; RL11_HUMAN. |
研究领域 | 肿瘤 细胞生物 免疫学 生长因子和激素 |
抗体来源 | Rabbit |
克隆类型 | Polyclonal |
交叉反应 | Mouse, Rat, (predicted: Human, Dog, Pig, ) |
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 | 20kDa |
细胞定位 | 细胞核 |
性 状 | Liquid |
浓 度 | 1mg/ml |
免 疫 原 | KLH conjugated synthetic peptide derived from human RPL11/GIG34:101-178/178 |
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 | Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L5P family of ribosomal proteins. It is located in the cytoplasm. The protein probably associates with the 5S rRNA. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Dec 2010]. Function: Binds to 5S ribosomal RNA (By similarity). Required for rRNA maturation and formation of the 60S ribosomal subunits. Promotes nucleolar location of PML (By similarity). Subunit: Interacts with PML and MDM2 (By similarity). Subcellular Location: Nucleus, nucleolus (By similarity). DISEASE: Diamond-Blackfan anemia 7 (DBA7) [MIM:612562]: A form of Diamond-Blackfan anemia, a congenital non-regenerative hypoplastic anemia that usually presents early in infancy. Diamond-Blackfan anemia is characterized by a moderate to severe macrocytic anemia, erythroblastopenia, and an increased risk of malignancy. 30 to 40% of Diamond-Blackfan anemia patients present with short stature and congenital anomalies, the most frequent being craniofacial (Pierre-Robin syndrome and cleft palate), thumb and urogenital anomalies. Note=The disease is caused by mutations affecting the gene represented in this entry. Similarity: Belongs to the ribosomal protein L5P family. SWISS: P62913 Gene ID: 6135 Database links: Entrez Gene: 6135 Human Entrez Gene: 67025 Mouse Omim: 604175 Human SwissProt: P62913 Human SwissProt: Q9CXW4 Mouse Unigene: 719951 Human Unigene: 276856 Mouse Unigene: 129770 Rat Unigene: 14687 Rat Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |