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Rabbit Anti-MAGIX/AF555 Conjugated antibody
Rabbit Anti-MAGIX/AF555 Conjugated antibody
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.
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  • NO.:SL18630R-AF555
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:Human,
    Applications:ICC IF
    concentration:1mg/ml
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Product Name Anti-MAGIX/AF555
Chinese Name AF555标记的MAGIX蛋白抗体
Alias 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.  
Research Area Cell biology  immunology  Developmental biology  
Immunogen Species Rabbit
Clonality Polyclonal
React Species Human, 
Applications ICC=1:50-200 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Molecular weight 35kDa
Form Lyophilized or Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human MAGIX
Lsotype IgG
Purification affinity purified by Protein A
Storage Buffer 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol
Storage 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.
Product Detail 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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