Product Name
MKRN3, Polyclonal Antibody
Popular Item
Full Product Name
MKRN3 Polyclonal Antibody
Product Synonym Names
MKRN3; CPPB2; D15S9; RNF63; ZFP127; ZNF127; makorin ring finger protein 3
Product Gene Name
anti-MKRN3 antibody
[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
3D Structure
ModBase 3D Structure for Q13064
Species Reactivity
Human, Mouse
Purity/Purification
Affinity Purification
Form/Format
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Concentration
3.71 mg/ml (lot specific)
Immunogen
Recombinant fusion protein containing a sequence corresponding to amino acids 1-260 of human MKRN3 (NP_005655.1).
Immunogen Sequence
MEEPAAPSEAHEAAGAQAGAEAAREGVSGPDLPVCEPSGESAAPDSALPHAARGWAPFPVAPVPAHLRRGGLRPAPASGGGAWPSPLPSRSSGIWTKQIICRYYIHGQCKEGENCRYSHDLSGRKMATEGGVSPPGASAGGGPSTAAHIEPPTQEVAEAPPAASSLSLPVIGSAAERGFFEAERDNADRGAAGGAGVESWADAIEFVPGQPYRGRWVASAPEAPLQSSETERKQMAVGSGLRFCYYASRGVCFRGESCMY
Positive Samples
Mouse Kidney
Preparation and Storage
Store at -20 degree C. Avoid freeze/thaw cycles.
Other Notes
Small volumes of anti-MKRN3 antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Related Product Information for
anti-MKRN3 antibody
The protein encoded by this gene contains a RING (C3HC4) zinc finger motif and several C3H zinc finger motifs. This gene is intronless and imprinted, with expression only from the paternal allele. Disruption of the imprinting at this locus may contribute to Prader-Willi syndrome. An antisense RNA of unknown function has been found overlapping this gene.
Applications Tested/Suitable for anti-MKRN3 antibody
Western Blot (WB)
Application Notes for anti-MKRN3 antibody
WB: 1:500-1:2000
Western Blot (WB) of anti-MKRN3 antibody
Western blot-MKRN3 Polyclonal Antibody

NCBI/Uniprot data below describe general gene information for MKRN3. It may not necessarily be applicable to this product.
NCBI Accession #
NP_005655.1
[Other Products]
NCBI GenBank Nucleotide #
NP_005655.1
[Other Products]
UniProt Primary Accession #
Q13064
[Other Products]
UniProt Related Accession #
Q13064[Other Products]
Molecular Weight
Calculated: 55kDa
Observed: 56kDa
NCBI Official Full Name
probable E3 ubiquitin-protein ligase makorin-3
NCBI Official Synonym Full Names
makorin ring finger protein 3
NCBI Official Symbol
MKRN3 [Similar Products]
NCBI Official Synonym Symbols
CPPB2; D15S9; RNF63; ZFP127; ZNF127
[Similar Products]
NCBI Protein Information
probable E3 ubiquitin-protein ligase makorin-3
UniProt Protein Name
Probable E3 ubiquitin-protein ligase makorin-3
UniProt Synonym Protein Names
RING finger protein 63; RING-type E3 ubiquitin transferase makorin-3Curated; Zinc finger protein 127
Protein Family
Probable E3 ubiquitin-protein ligase makorin
UniProt Gene Name
MKRN3 [Similar Products]
UniProt Synonym Gene Names
D15S9; RNF63; ZNF127 [Similar Products]
NCBI Summary for MKRN3
The protein encoded by this gene contains a RING (C3HC4) zinc finger motif and several C3H zinc finger motifs. This gene is intronless and imprinted, with expression only from the paternal allele. Disruption of the imprinting at this locus may contribute to Prader-Willi syndrome. An antisense RNA of unknown function has been found overlapping this gene. [provided by RefSeq, Jul 2008]
UniProt Comments for MKRN3
MKRN3: E3 ubiquitin ligase catalyzing the covalent attachment of ubiquitin moieties onto substrate proteins.
Protein type: EC 6.3.2.-; EC 6.3.2.19; Ubiquitin conjugating system; Ubiquitin ligase
Chromosomal Location of Human Ortholog: 15q11.2
Cellular Component: intracellular ribonucleoprotein complex
Molecular Function: identical protein binding; metal ion binding; protein binding; transferase activity
Biological Process: protein ubiquitination
Disease: Prader-willi Syndrome; Precocious Puberty, Central, 2
Research Articles on MKRN3
1. MKRN3 DMR was found aberrantly hypermethylated in all control and AS iPSCs, regardless of the methylation status of the PWS-IC master regulator. This suggests a loss of hierarchical control of imprinting at PWS/AS region.
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