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Rabbit Anti-MAGIX/BF488 Conjugated antibody (bs-18630R-BF488)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-18630R-BF488
英文名稱 Rabbit Anti-MAGIX/BF488 Conjugated antibody
中文名稱 BF488標記的MAGIX蛋白抗體
別    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.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 細胞生物  免疫學  發育生物學  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Human, 
產品應用 ICC=1:50-200 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 35kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human MAGIX
亞    型 IgG
純化方法 affinity purified by Protein A
儲 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol
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.
產品介紹 background:
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.

Database links:

Entrez Gene: 79917 Human

SwissProt: Q9H6Y5 Human

Unigene: 193170 Human



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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