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ZNF198 Antibody

ZNF198 contains nine MYM-type zinc fingers. The N-terminal half of the ZNF198 gene has been identified as a gene fused to the cytoplasmic domain of the fibroblast growth factor receptor (FGFR1) gene as a result of a t(8;13) (p11;q11-12) chromosomal rearrangement. The t(8;13) chromosomal translocation is associated with myeloproliferative diseases such as stem cell leukemia lymphoma syndrome (SCLL). Studies of the normal function of ZNF198 have revealed that it associates with HHR6 and RAD18 and may be involved in the repair of DNA. ZNF198 has also been found to associate with the BHC110 subunit of a histone-deacetylase containing corepressor complex and may have an additional function in transcriptional repression.
ZMYM2
zinc finger MYM-type containing 2
Zinc finger MYM-type protein 2
:  FIM fused in myeloproliferative disorders protein MYM RAMP rearranged in an atypical myeloproliferative disorder Rearranged in atypical myeloproliferative disorder protein SCLL zinc finger MYM-type protein 2 zinc finger protein 198 zinc finger, MYM-type 2 ZNF198 More... Less...
Product
Specifications
Ordering Information
Human
WB, IP
between 150 and 200
$367
$247
$103
Human
WB, IP
between 975 and 1025
$367
$247
$103
Human
WB, IP, IHC
between 1327 and 1377
$367
$247
$103
Human, Mouse
IHC
Between 1327 and 1377
$389
$103