*红钠盐号:34487-61-1
*红钠盐号:34487-61-1
*红钠盐号:34487-61-1
*红钠盐号:34487-61-1

*红钠盐号:34487-61-1

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*红钠盐号:34487-61-1一在0℃~10℃之间冷藏保存(原则上保存在15℃以下的阴凉处),但相对于产品运输时,并不是所有产品的运输温度与储存温度*,冷冻保存的温度在0℃以下。有些产品

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*红钠盐号:34487-61-1   
英文名称:Phenol red sodium salt;Phenolsulfonephthalein sodium salt    
其他名称:酚红钠;水溶性酚红钠盐;*磺钛钠   
号:34487-61-1    
C19H13NaO5S=376.36    
级别:IND   
纯度:≥95.0%   
pH变色域:6.5(黄)~8.0(红)   
性状(以下信息仅供参考):暗红至棕红色结晶或粉末,溶于水,微溶于醇,熔点285℃   
用途:本品仅供科研,不得用于其它用途。(以下用途仅供参考)酸碱指示剂;血液二氧化碳全量测定。细菌血清检验中制备双糖铁尿素培养基的指示剂等   
保存:RT 
客户根据*红钠盐号:34487-61-1性质、化学式、分子式、结构式、比重、密度、号、沸点、熔点、水溶性、MSDS、用途、作用、规格包装、性状、注意事项、英文名、别称、纯度、级别等情况,本产品化学性质稳定,运输条件不苛刻,一般储存在阴凉,干燥,通风良好的地方,远离不相容的物质。保持容器密闭。
试剂品牌:TCI、sigma、Alfa、Avocado、Aldrich、ACROS、Fluka、ICN(MP)等
包装:1kg、100g、10g、250g、25g、500g、50g、5g等包装
级别:GR级别、AR级别、CP级别、L.P.级别等
公司提供的*红钠盐号:34487-61-1*,货源充足。严格的生产质量控制体系,包括:优级纯,分析纯,化学纯,试剂级,基准试剂,实验纯,教学试剂,高纯试剂,色谱纯,光谱纯,电子纯。各种包装规格,并可提供包装定制,咨询订购

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Function : Neuronal cell surface protein that may be involved in cell recognition and cell adhesion. May mediate intracellular signaling.
Subunit : Interacts (via laminin G-like domain 2 and/or laminin G-like domain 6) with NLGN1 forming a heterotetramer, where one NLGN1 dimer interacts with one NRXN1 dimer. Interacts (via laminin G-like domain 2 and/or laminin G-like domain 6) with NLGN1, NLGN2, NLGN3, NLGN4X and NLGN4Y; these interactions are calcium-dependent. Interacts (via laminin G-like domain 2) with NXPH1 and NXPH3. Interacts with CBLN1 and CBLN2. Interacts with LRRTM1, LRRTM2, LRRTM3 and LRRTM4 (By similarity). Alpha-type isoforms (neurexin-1-alpha) interact (via laminin G-like domain 2 and/or laminin G-like domain 6) with DAG1 (via alpha-dystroglycan chain). Alpha-type isoforms interact with alpha-latroxin from spider venom. The cytoplasmic C-terminal region binds to K, KIN1 and APBA1. Interacts with SYT13 and SYTL1 (By similarity).
*红钠盐号:34487-61-1Subcellular Location : Membrane.
Tissue Specificity : Heart and brain.
Post-translational modifications : N-glycosylated (By similarity).
O-glycosylated (By similarity).
Similarity : Belongs to the neurexin family.
Contains 3 EGF-like domains.
Contains 6 laminin G-like domains.
Database links : UniProtKB/Swiss-Prot: Q9ULB1.1
英文名称  Anti-Ninjurin 1
中文名称  神经损伤诱导蛋白1抗体
别    名  Nerve injury induced protein 1; Nerve injury-induced protein 1; NIN1; NINJ1; NINJ1_HUMAN; NINJURIN; Ninjurin-1.
浓    度  1mg/1ml
规 格  0.2ml/200μg
抗体来源  Rabbit 
克隆类型  polyclonal
交叉反应  Human, Mouse, Rat, Chicken, Dog, Cow, Rabbit, Sheep
产品类型  一抗   
研究领域  神经生物学 细胞粘附分子 细胞膜蛋白 
蛋白分子量  predicted molecular weight: 16kDa
性    状  Lyophilized or Liquid
免 疫 原  KLH conjugated synthetic peptide derived from human Ninjurin 1
亚    型  IgG
纯化方法  affinity purified by Protein A
储 存 液  Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4
产品应用   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. 
保存条件  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.
产品介绍 Ninjurin family proteins are muli-pass membrane proteins induced by nerve injury in Schwann cells and dorsal root ganglion neurons. Nunjurin proteins act as homophilic cell adhesion molecules that promote axonal growth. Ninjurin proteins also play a role in the formation and function of other tissues. Ninjurin-1 is widely expressed in adult and embryonic tissues, particularly those with epithelial origin. Ninjurin-2 is also widely expressed, with highest levels in adult bone marrow and peripheral blood lymphocytes and embryo liver, thymus and heart. The genes that encode the Ninjurin proteins map to a region known to cause several genetic disorders, including hereditary sensory neuropathy type I and type II (HSN1 and HSN2). However, no link between mutations in the genes encoding Ninjurins and the diseases have been found.

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