SKU: WP17483 Categories: ,

ZFP57 rabbit pAb

Price range: $268.00 through $328.00

SKU: WP17483-100
Enter the quantity you would like, or drag the panel to find the quantity and price that best for you
Bulk QuoteAuthorize OEM & ODM

Product details

Background:

The protein encoded by this gene is a zinc finger protein containing a KRAB domain. Studies in mouse suggest that this protein may function as a transcriptional repressor. Mutations in this gene have been associated with transient neonatal diabetes mellitus type 1 (TNDM1).[provided by RefSeq, Sep 2009],

Specifications

Size50μL/100μL
TargetZFP57
ReactivityHuman, Mouse, Rat
ApplicationsWB
MW(Calculated)50kD
MW(Observed)
Host SpeciesRabbit
IsotypeIgG
Conjugate/ModificationUnmodified
Recommended Dilution RatioWB 1:500-2000
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration1 mg/ml
ClonalityPolyclonal
Clone Number
ImmunogenSynthesized peptide derived from human ZFP57 AA range: 373-423
SpecificityThis antibody detects endogenous levels of ZFP57 at Human/Mouse/Rat
Gene NameZFP57 C6orf40 ZNF698
Protein NameZFP57
Other Name
SpeciesHuman
Gene ID346171
UniprotQ9NU63,
Species.1Mouse
Gene ID.122715
Uniprot.1Q8C6P8,
Species.2Rat
Gene ID.2361783
Uniprot.2A0JPK3
Cellular LocalizationNucleus . Binds various differentially methylated regions (DMR). .
Tissue Expression
Signaling_pathway
Research Areas>>Herpes simplex virus 1 infection
FunctionDisease:Defects in ZFP57 are the cause of transient neonatal diabetes mellitus type 1 (TNDM1) [MIM:601410]. Neonatal diabetes is a form of diabetes mellitus defined by the onset of mild-to-severe hyperglycemia within the first months of life. In about half of the neonates, diabetes is transient and resolves at a median age of 3 months, whereas the rest have a permanent form of diabetes. The major cause of TNDM1 is aberrant expression of imprinted genes at chromosome 6q24, associated in 20% of cases with DNA hypomethylation at the transient neonatal diabetes differentially methylated region (DMR), which lies within the imprinted promoter of the PLAGL1 gene. Over 50% of individuals with transient neonatal diabetes and hypomethylation at 6q24 also show mosaic DNA hypomethylation at other imprinted loci throughout the genome and a range of additional clinical features.,Domain:The KRAB domain is required for function as transcriptional repressor.,Function:Transcription regulator required to maintain maternal and paternal gene imprinting, a process by which gene expression is restricted in a parent of origin-specific manner by epigenetic modification of genomic DNA and chromatin, including DNA methylation. Acts by controlling DNA methylation during the earliest multicellular stages of development at multiple imprinting control regions. Required for the establishment of maternal methylation imprints at SNRPN locus. Acts as a transcriptional repressor in Schwann cells.,similarity:Belongs to the krueppel C2H2-type zinc-finger protein family. ZFP57 subfamily.,similarity:Contains 1 KRAB domain.,similarity:Contains 7 C2H2-type zinc fingers.,subcellular location:Binds various differentially methylated regions (DMR), including the Snrpn DMR.,
Please login to post questions
Back to Top
Product has been added to your cart