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Rabbit Anti-C9orf153 antibody
Rabbit Anti-C9orf153 antibody
bA507D14.1; Chromosome 9 open reading frame 153; Hypothetical protein LOC389766; MGC131702; Uncharacterized protein C9orf153;
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Details

Product Name C9orf153
Chinese Name 9号染色体开放阅读框153抗体
Alias bA507D14.1; Chromosome 9 open reading frame 153; Hypothetical protein LOC389766; MGC131702; Uncharacterized protein C9orf153;   
Research Area Cell biology  immunology  Developmental biology  
Immunogen Species Rabbit
Clonality Polyclonal
React Species (predicted: Human, )
Applications WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (Paraffin sections need antigen repair)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Theoretical molecular weight 11kDa
Form Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human C9orf153: 1-80/101 
Lsotype IgG
Purification affinity purified by Protein A
Buffer Solution 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Storage Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
Attention This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
Product Detail C9orf153 is a 101 amino acid protein that exists as two alternatively spliced isoforms. The gene encoding C9orf153 maps to human chromosome 9q21.33. 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.

SWISS:
Q5TBE3

Gene ID:
389766

Database links:

Entrez Gene: 389766 Human

SwissProt: Q5TBE3 Human



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