FAM50C Rabbit Polyclonal Antibody
No Size Price Availability  
YRP08320-01 50ul 1500.00 In Stock
YRP08320-01 100ul 2000.00 In Stock
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Source: Rabbit Gene Id: 51307
Isotype: IgG Swiss Prot:
purity: Purified by Protein A.
Background:
With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome. The FAM53C gene product has been provisionally designated FAM53C pending further characterization.
Reactivity Human, Mouse, Rat
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 FAM50C
Storage Aqueous buffered solution containing 100ug/ml BSA, 50% glycerol and 0.09% sodium azide. Store at -20℃ for 12 months
Synonym C5orf6, FA53C_HUMAN, Fam53c, Family with sequence similarity 53 member C, Hypothetical protein LOC51307, Protein FAM53C.
This product is for research use only, not for diagnostic or therapeutic use!

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