甲基紅鈉號：845-10-3   
英文名稱：Methyl red sodium salt；p-Dimethylaminoazobenzene-o-carboxylic acid sodium salt；C.I. 13020；2-[4-(Dimethylamino)phenylazo]benzoic acid sodium salt   
其他名稱：甲基紅鈉鹽；2-[4-(二甲基氨基)苯基偶氮]*鹽；水溶性甲基紅；對二甲氨基偶氮苯鄰羧酸鈉；4-二甲氨基偶氮苯-2' -羧酸鈉鹽   
號：845-10-3    
C15H14N3NaO2=291.28   
級別：IND   
pH變色域：4.5(紅)～6.2(黃)   
乙醇溶解試驗：合格    
性狀(以下信息僅供參考)：橙紅色結晶粉末。溶于水和乙醇。Z大吸收波長437nm   
用途：本品僅供科研，不得用于其它用途。(以下用途僅供參考)酸堿指示劑，pH變色范圍4.4(紅)～6.2(黃)。氧化還原指示劑。用于硫酸鈰滴定亞鐵離子   
保存：RT，避光
甲基紅鈉號：845-10-3儲存條件：
避光、干燥陰涼處封閉貯存,嚴禁與有毒、有害物品混放、混運。本品為非危險 產品可按一般化學品運輸,輕搬動輕放,防止日曬、雨淋！受熱、受潮、受光后易喪失活力,保存期短,因此貯存和運輸條件比較苛刻。
運輸：汽車運輸、EMS郵政快遞，申通快遞等， 款到上海3天內發貨；
售后：如您對我們的產品服務及技術指標有特殊要求，請及時通知我方。
存儲：應貯存在干燥清潔避光的環境中，嚴禁與有毒物質混放，以免污染（保質期為兩年）。
甲基紅鈉號：845-10-3主要優級純、分級純和化學純3種：
（1）優級純（GR：Guaranteed reagent），又稱一級品或保證試劑，99.8%，這種試劑純度Z高，雜質含量Z低，適合于重要精密的分析工作和科學研究工作，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、學校一般分析工作。使用藍色（深藍色）標簽。
（4）實驗試劑（LR：Laboratory reagent），又稱四級試劑。
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CAMs has proven important for learning and memory. Proper embryonic morphogenic development is also heavily dependent on the regulation of cell adhesion molecules. Neurotrimin (hNT) is a neural cell adhesion molecule localizing to the cell membrane, where it acts as a lipid-anchor. Neurotrimin belongs to the IgLON family of proteins, a member of the larger immunoglobulin superfamily.
Function : Neural cell adhesion molecule.
Subunit : Belongs to the immunoglobulin superfamily. IgLON family. Contains 3 Ig-like C2-type (immunoglobulin-like) domains.
Subcellular Location : Cell membrane.
Similarity : Belongs to the immunoglobulin superfamily. IgLON family.
Contains 3 Ig-like C2-type (immunoglobulin-like) domains.
Database links : UniProtKB/Swiss-Prot: Q9P121.1
英文名稱  Anti-NLGN4X
中文名稱  神經元X連鎖蛋白/兒童自閉癥相關蛋白抗體
別    名  X-linked; HNLX; KIAA1260; Neuroligin X; Neuroligin-4; NLGN4; NLGN 4; NLGN4X; Neuroligin 4 X linked; Neuroligin 4; Neuroligin X; NLGN; NLGN-4; NLGN4X; NLGN4Y; NLGNX_HUMAN.
濃    度  1mg/1ml
規 格  0.2ml/200μg
抗體來源  Rabbit 
克隆類型  polyclonal
交叉反應  Human, Mouse, Rat, Dog, Pig, Horse, Zebrafish, Chimpanzee, mpanzee
產品類型  一抗   
研究領域  發育生物學 神經生物學 細胞粘附分子 細胞膜蛋白 
蛋白分子量  predicted molecular weight: 92kDa
性    狀  Lyophilized or Liquid
免 疫 原  KLH conjugated synthetic peptide derived from human NLGN4X
亞    型  IgG
純化方法  affinity purified by Protein A
甲基紅鈉號：845-10-3儲 存 液  Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4
產品應用   WB=1:100-500  ELISA=1:500-1000  IHC-P=1:100-500  IHC-F=1:100-500  Flow-Cyt=1:100-500  ICC=1:100-500  IF=1:100-500
（石蠟切片需做抗原修復）
 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.
產品介紹 This gene encodes a member of a family of neuronal cell surface proteins. Members of this family may act as splice site-specific ligands for beta-neurexins and may be involved in the formation and remodeling of central nervous system synapses. The encoded protein interacts with discs, large (Drosophila) homolog 4 (DLG4). Mutations in this gene have been associated with autism and Asperger syndrome. Two transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jul 2008].
Function : Putative neuronal cell surface protein involved in cell-cell-interactions.
Subunit : Belongs to the type-B carboxylesterase/lipase family.
Subcellular Location : Membrane.
Tissue Specificity : Expressed at highest levels in heart. Expressed at lower levels in liver, skeletal muscle and pancreas and at very low levels in brain.
DISEASE : Defects in NLGN4X may be the cause of susceptibility to autism X-linked type 2 (AUTSX2). AUTSX2 is a pervasive developmental disorder (PDD), prototypically characterized by impairments in reciprocal social interaction and communication, restricted and stereotyped patterns of interests and activities, and the presence of developmental abnormalities by 3 years of age. Defects in NLGN4X may be the cause of susceptibility to X-linked Asperger syndrome 2 (ASPGX2). ASPGX2 is considered to be a form of childhood autism.
Similarity : Belongs to the type-B carboxylesterase/lipase family.