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Rabbit Anti-C9orf131/AF488 Conjugated antibody
Rabbit Anti-C9orf131/AF488 Conjugated antibody
C9orf131; Chromosome 9 open reading frame 131; CI131_HUMAN; MGC41945; Uncharacterized protein C9orf131.
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  • NO.:SL15311R-AF488
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:Human,
    Applications:ICC IF
    concentration:1mg/ml
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Product Name Anti-C9orf131/AF488
Chinese Name AF488标记的9号染色体开放阅读框131抗体
Alias C9orf131; Chromosome 9 open reading frame 131; CI131_HUMAN; MGC41945; Uncharacterized protein C9orf131.   
Research Area Cell biology  immunology  
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 118kDa
Form Lyophilized or Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human C9orf131
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:
C9orf131 (chromosome 9 open reading frame 131) is a 1,079 amino acid protein encoded by a gene that maps to human chromosome 9p13.3. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.

Database links:

Entrez Gene: 138724 Human

SwissProt: Q5VYM1 Human

Unigene: 148250 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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