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偶氮胭脂紅G 號：25641-18-3  
英文名稱：Azocarmine G；Rosinduline GXF；Rosazine；Rosinduline；N-Phenylrosinduline sulfonic acid disodium salt；

C.I.50085   
其他名稱：酸性紅101；偶氮洋紅G；玫紅對氮蒽；偶氮紅G；羅星杜林；玫紅杜林   
號：25641-18-3   
C28H18N3NaO6S2=579.58   
級別：BS   
鑒別：合格   
λmax：523～526nm (H2O)   
性狀(以下信息僅供參考)：帶金黃色光澤的紅色或棕色或紫色粉末。微溶于水,溶液呈藍紅色。   
用途：本品僅供科研，不得用于其它用途。(以下用途僅供參考)組織染色。氧化還原指示劑。   
保存：RT

客戶根據偶氮胭脂紅G 號：25641-18-3性質、化學式、分子式、結構式、比重、密度、號、沸點、熔點、水溶性、MSDS、用途、作用、規(guī)格包裝、性狀、注意事項、英文名、別稱、純度、級別等情況，本產品化學性質穩(wěn)定，運輸條件不苛刻，一般儲存在陰涼，干燥，通風良好的地方，遠離不相容的物質。保持容器密閉。
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DISEASE : Neurofibromatosis 1 (NF1) [MIM:162200]: A disease characterized by patches of skin pigmentation (cafe-au-lait spots), Lisch nodules of the iris, tumors in the peripheral nervous system and fibromatous skin tumors. Individuals with the disorder have increased susceptibility to the development of benign and malignant tumors. Note=The disease is caused by mutations affecting the gene represented in this entry.
Leukemia, juvenile myelomonocytic (JMML) [MIM:607785]: An aggressive pediatric myelodysplastic syndrome/myeloproliferative disorder characterized by malignant transformation in the hematopoietic stem cell compartment with proliferation of differentiated progeny. Patients have splenomegaly, enlarged lymph nodes, rashes, and hemorrhages. Note=The disease is caused by mutations affecting the gene represented in this entry.
Watson syndrome (WS) [MIM:193520]: A syndrome characterized by the presence of pulmonary stenosis, cafe-au-lait spots, and mental retardation. It is considered as an atypical form of neurofibromatosis. Note=The disease is caused by mutations affecting the gene represented in this entry.
Familial spinal neurofibromatosis (FSNF) [MIM:162210]: Considered to be an alternative form of neurofibromatosis, showing multiple spinal tumors. Note=The disease is caused by mutations affecting the gene represented in this entry.
Neurofibromatosis-Noonan syndrome (NFNS) [MIM:601321]: Characterized by manifestations of both NF1 and Noonan syndrome (NS). NS is a disorder characterized by dysmorphic facial features, short stature, hyperorism, cardiac anomalies, deafness, motor delay, and a bleeding diathesis. Note=The disease is caused by mutations affecting the gene represented in this entry.
Colorectal cancer (CRC) [MIM:114500]: A complex disease characterized by malignant lesions arising from the inner wall of the large intestine (the colon) and the rectum. Genetic alterations are often associated with progression from premalignant lesion (adenoma) to invasive adenocarcinoma. Risk factors for cancer of the colon and rectum include colon polyps, long-standing ulcerative colitis, and genetic family history. Note=The gene represented in this entry may be involved in disease pathogenesis.
Similarity : Contains 1 CRAL-TRIO domain.
Contains 1 Ras-GAP domain.
Database links : UniProtKB/Swiss-Prot: P21359.2
英文名稱  Anti-Phospho-NFKB1(Ser373)
偶氮胭脂紅G 號：25641-18-3中文名稱  磷酸化細胞核因子p50/k基因結合核因子抗體
別    名  Phospho-NFKB1(Ser373); NFKB1(phospho S373); NF kappa B; NFKB 1; NFKB p105; NFKB p50; NFKB1; Nuclear factor kappa B DNA binding subunit; Nuclear factor NF kappa B p105 subunit; Nuclear factor NF kappa B p50 subunit; Nuclear factor of kappa light polypeptide gene enhancer in B cells 1; DKFZp686C01211; DNA binding factor KBF1; DNA binding factor KBF1 EBP1; EBP 1; EBP1; KBF1; MGC54151; nuclear factor of kappa light polypeptide gene enhancer in B-cells 1; Nfkb1; NF-kappaB; NF-kappaB1; NF-KB1; p105; p50; p50/p105; DKFZp686C01211; EBP-1; KBF1; MGC54151; Nf kappa b DNA binding subunit; NF-KAPPAB; NF-KAPPAB1; NFKB; NFKB SUBUNIT P105/P50; NFKB-p105; NFKB1; NUCLEAR FACTOR KAPPA B DNA BINDING SUBUNIT; p105 Nfkb;p50 NF-kappa B;p50NFKB.
濃    度  1mg/1ml
規(guī) 格  0.1ml/100μg
抗體來源  Rabbit 
克隆類型  polyclonal
交叉反應  Human, Mouse, Rat, Pig, Cow, Horse, Sheep
產品類型  一抗  磷酸化抗體  
研究領域  腫瘤 細胞生物 免疫學 信號轉導 細胞凋亡 轉錄調節(jié)因子 激酶和磷酸酶 
蛋白分子量  predicted molecular weight: 105kDa
性    狀  Lyophilized or Liquid