亮綠SF（淡黃）號：5141-20-8   
英文名稱：Light green SF yellowish；Light green 2G,S or 2GN；Acid green；C.I. 42095   
其他名稱：酸性綠5；亮綠(淡黃)；亮綠2G；亮綠S；亮綠2GN；酸性綠；黃色淺綠SF；淡綠SF淡黃；黃光亮綠；酸性綠 SF   
號：5141-20-8    
C37H34N2O9S3Na2=792.85   
級別：FMP   
含量：≥85.0%   
Em (Lambda Max, Water)：>63500   
性狀(以下信息僅供參考)：深紫色或紅棕色結(jié)晶或結(jié)晶粉末。易溶于水呈綠色溶液，加入鹽酸則轉(zhuǎn)為黃棕色，以后漸漸褪色。加入氫氧化鈉則幾乎全部褪色，析出暗紫色沉淀。熔點(diǎn)288℃(分解)，Z大吸收波長630(422)nm。   
用途：本品僅供科研，不得用于其它用途。(以下用途僅供參考)用作細(xì)胞學(xué)上的復(fù)染色，或Gomori's步驟中用作苯胺蘭的替代物。漿質(zhì)染色劑。動(dòng)物組織染色。與鐵蘇木素或其他核染料作對比染色。植物組織學(xué)中作細(xì)胞質(zhì)和纖維染色。和酸性品紅共染花粉管   
保存：RT 亮綠SF（淡黃）號：5141-20-8儲(chǔ)存條件：
避光、干燥陰涼處封閉貯存,嚴(yán)禁與有毒、有害物品混放、混運(yùn)。本品為非危險(xiǎn) 產(chǎn)品可按一般化學(xué)品運(yùn)輸,輕搬動(dòng)輕放,防止日曬、雨淋！受熱、受潮、受光后易喪失活力,保存期短,因此貯存和運(yùn)輸條件比較苛刻。
運(yùn)輸：汽車運(yùn)輸、EMS郵政快遞，申通快遞等， 款到上海3天內(nèi)發(fā)貨； 
售后：如您對我們的產(chǎn)品服務(wù)及技術(shù)指標(biāo)有特殊要求，請及時(shí)通知我方。 
存儲(chǔ)：應(yīng)貯存在干燥清潔避光的環(huán)境中，嚴(yán)禁與有毒物質(zhì)混放，以免污染（保質(zhì)期為兩年）。 
亮綠SF（淡黃）號：5141-20-8主要優(yōu)級純、分級純和化學(xué)純3種：
（1）優(yōu)級純（GR：Guaranteed reagent），又稱一級品或保證試劑，99.8%，這種試劑純度Z高，雜質(zhì)含量Z低，適合于重要精密的分析工作和科學(xué)研究工作，使用綠色瓶簽。
（2）分析純（AR），又稱二級試劑，純度很高，99.7%，略次于優(yōu)級純，適合于重要分析及一般研究工作，使用紅色瓶簽。
（3）化學(xué)純（CP），又稱三級試劑，≥ 99.5%，純度與分析純相差較大，適用于工礦、學(xué)校一般分析工作。使用藍(lán)色（深藍(lán)色）標(biāo)簽。
（4）實(shí)驗(yàn)試劑（LR：Laboratory reagent），又稱四級試劑。
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17q 2-32.
Function : Aminopeptidase with broad substrate specificity for several peptides. Involved in proteolytic events essential for cell growth and viability. May act as regulator of neuropeptide activity. Plays a role in the antigen-processing pathway for MHC class I molecules. Involved in the N-terminal trimming of cytotoxic T-cell epitope precursors. Digests the poly-Q peptides found in many cellular proteins. Digests tau from normal brain more efficiently than tau from Alzheimer disease brain.
Subcellular Location : Cytoplasm
Tissue Specificity : Detected in liver, epithelium of renal tubules, epithelium of small and large intestine, gastric epithelial cells, and alveoli of the lung (at protein level).
Similarity : Belongs to the peptidase M1 family.
英文名稱  Anti-NDSP/FAM163A
中文名稱  神經(jīng)母細(xì)胞瘤源性分泌蛋白抗體
別    名  C1orf76; Chromosome 1 open reading frame 76; F163A_HUMAN; Fam163a; hypothetical protein MGC16664; NDSP; Neuroblastoma derived secretory protein; Neuroblastoma-derived secretory protein; Protein FAM163A
濃    度  1mg/1ml
規(guī) 格  0.2ml/200μg
抗體來源  Rabbit 
克隆類型  polyclonal
交叉反應(yīng)  Human, Mouse, Rat, Dog, Pig, Cow, Horse, Sheep
產(chǎn)品類型  一抗   
研究領(lǐng)域  腫瘤 細(xì)胞生物 神經(jīng)生物學(xué) 
蛋白分子量  predicted molecular weight: 18kDa
性    狀  Lyophilized or Liquid
免 疫 原  KLH conjugated synthetic peptide derived from human NDSP (121-167aa)
亞    型  IgG
純化方法  affinity purified by Protein A
儲(chǔ) 存 液  Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4
產(chǎn)品應(yīng)用   WB=1:100-500  ELISA=1:500-1000  IHC-P=1:100-500  IHC-F=1:100-500  ICC=1:100-500  IF=1:100-500
（石蠟切片需做抗原修復(fù)）
亮綠SF（淡黃）號：5141-20-8 not yet tested in other applications.
 optimal dilutions/concentrations should be determined by the end user. 
保存條件  Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
Important Note  This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
產(chǎn)品介紹 Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf76 gene product has been provisionally designated C1orf76 pending further characterization.
Subcellular Location : Membrane; Single-pass membrane protein (Potential).
Tissue Specificity : Highly expressed in neuroblastoma compared to other tissues, suggesting that it may be used
亞    型  IgG