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Rabbit Anti-C9orf116/AP Conjugated antibody
Rabbit Anti-C9orf116/AP Conjugated antibody
C9orf116; CI116_HUMAN; Pierce 1; UPF0691 protein C9orf116.
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  • NO.:SL15310R-AP
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:(predicted: Human,Mouse,Rat,Dog,Pig,Cow,Sheep,)
    Applications:WB IHC-P IHC-F ICC
    concentration:1mg/ml
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Details

Product Name Anti-C9orf116/AP
Chinese Name 碱性磷酸酶(AP)标记的9号染色体开放阅读框116抗体
Alias C9orf116; CI116_HUMAN; Pierce 1; UPF0691 protein C9orf116.   
Research Area Cell biology  immunology  
Immunogen Species Rabbit
Clonality Polyclonal
React Species (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Sheep, )
Applications WB=1:50-200 IHC-P=1:50-200 IHC-F=1:50-200 ICC=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Molecular weight 15kDa
Form Lyophilized or Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human C9orf116
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:
C9orf116 is a 136 amino acid protein that belongs to the UPF0691 family. Pierce 1 exists as two alternatively spliced isoforms, which are conserved in chimpanzee, dog, cow, mouse and rat. Pierce 1 is predominantly expressed in micrometastases and macrometastases of human small cell lung cancer. Pierce 1 is encoded by a gene that maps to chromosome 9, which consists of about 145 million bases, makes up 4% of the human genome and encodes nearly 900 genes. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Considered 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 chromosome 9.

Similarity:
Belongs to the UPF0691 family.

Database links:

Entrez Gene: 138162 Human

Omim: 614502 Human

SwissProt: Q5BN46 Human

Unigene: 414028 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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