产品货号 : mlR18630
英文名称 : MAGIX
中文名称 : MAGIX蛋白抗体
别 名 : FLJ21687; JM10; MAGI family member, X-linked; MAGIX; MAGIX_HUMAN; MGC138889; PDZ domain containing protein; PDZ domain containing, X chromosome; PDZ domain-containing protein MAGIX; PDZX.
研究领域 : 细胞生物 免疫学 发育生物学
抗体来源 : Rabbit
克隆类型 : Polyclonal
交叉反应 : Human,
产品应用 : WB=1:500-2000 ELISA=1:500-1000 IHC-P=1:400-800 IHC-F=1:400-800 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.
分 子 量 : 35kDa
细胞定位 : 细胞浆
性 状 : Lyophilized or Liquid
浓 度 : 1mg/ml
免 疫 原 : KLH conjugated synthetic peptide derived from human MAGIX:201-300/334
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 : 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.
PubMed : PubMed
产品介绍 : MAGIX is a 334 amino acid protein that contains one PDZ (DHR) domain and exists as three alternatively spliced isoforms. The gene encoding MAGIX maps to human chromosome Xp11.23. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of a X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unusual number and combination of sex chromosomes being inherited, including Turner's syndrome, Klinefelter's syndrome and Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.
Similarity:
Contains 1 PDZ (DHR) domain.
SWISS:
Q9H6Y5
Gene ID:
79917
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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