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Product Description
C9orf72 Polyclonal Antibody | BS65435 | Bioworld
Host: Rabbit
Reactivity: Human,Mouse,Rat,Chicken,Dog,Pig,Cow,Horse,
Application: FCM,
Application Range: Flow-Cyt=1ug/test
Background: Chromosome 9 consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. 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 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. The C9orf72 gene product has been provisionally designated C9orf72 pending further characterization. There are two isoforms of C9orf72 that are produced as a result of alternative splicing events.
Storage & Stability: Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
Specificity: C9orf72 Polyclonal Antibody detects endogenous levels of C9orf72 protein.
Molecular Weight: 53kDa
Note: For research use only, not for use in diagnostic procedure.
Alternative Names: chromosome 9 open reading frame 72; CI072_HUMAN; MGC23980; Uncharacterized protein C9orf72.
Immunogen: KLH conjugated synthetic peptide derived from human C9orf72:391-481/481
Conjugate: Unconjugated
Modification: Unmodification
Purification & Purity: affinity purified by Protein A
Pathway:
