PHF8 Rabbit mAb (AMR11739N)
Product Specifications
Background
The protein encoded by this gene is a histone lysine demethylase that preferentially acts on histones in the monomethyl or dimethyl states. The encoded protein requires Fe (2+) ion, 2-oxoglutarate, and oxygen for its catalytic activity. Defects in this gene are a cause of mental retardation syndromic X-linked Siderius type (MRXSSD) . Four transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010]
Overview
We constantly strive to ensure we provide our customers with the best antibodies. As a result of this work we offer this antibody in purified format. We are in the process of updating our datasheets. If you have any questions regarding this update, please feel free to contact our technical support team. This product is a high quality PHF8 Rabbit mAb (APR24516N0) .
Synonyms
JHDM1F; KDM7B; MRXSSD; ZNF422
Gene ID
23133
UniProt
Q9UPP1
Dilution
WB 1:500 - 1:2000
Form
Liquid
Buffer
Buffer: PBS with 0.02% sodium azide, 0.05% BSA, 50% glycerol, pH7.3.
Molecular Weight
Calculated MW: 140kDa Observed MW: 140KDa
Storage Conditions
Store at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.
Gene ID URL
https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=gene&cmd=Retrieve&dopt=Graphics&list_uids=23133
Uniprot URL
https://www.uniprot.org/uniprot/Q9UPP1
AA Sequence
Email for sequence
Available Sizes
Frequently Asked Questions
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