C9ORF43 Rabbit Polyclonal Antibody
No Size Price Availability  
YRP09498-01 50ul 1500.00 In Stock
YRP09498-01 100ul 2000.00 In Stock
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Source: Rabbit Gene Id: 257169
Isotype: IgG Swiss Prot:
purity: Purified by Protein A.
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 C9orf43 gene product has been provisionally designated C9orf43 pending further characterization.
Reactivity Human
Tested applications WB IHC IF
Clonality Polyclonal Antibody
Calculated MW /
Recommended Dilutions
WB 1:100-1:1000
IHC 1:100-1:500
IF 1:50-1:200
Immunogen KLH conjugated synthetic peptide derived from human C9ORF43
Storage Aqueous buffered solution containing 100ug/ml BSA, 50% glycerol and 0.09% sodium azide. Store at -20℃ for 12 months
Synonym Uncharacterized protein C9orf43, Chromosome 9 open reading frame 43, Hypothetical protein LOC257169, MGC17358, CI043_HUMAN.
This product is for research use only, not for diagnostic or therapeutic use!

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