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A8451

DNA Polymerase gamma Rabbit polyclonal antibody

Size

£151.00

SKU:
A8451
Additional Names:
DNA Polymerase gamma|MDP1|MIRAS|MTDPS4A|MTDPS4B|PEO|POLG1|POLGA|SANDO|SCAE
Application:
ELISA, WB
Molecular Weight:
140kDa
Species Reactivity:
Human
Purification:
Affinity Purified
Storage Conditions:
-20[o]C Avoid freeze/thaw cycles.
Supplier:
Abclonal
Host:
Rabbit
Reactivities:
Human, Mouse, Rat
Immunogen:
Recombinant protein (or fragment).This information is considered to be commercially sensitive.
Formulation:
Unmodified
Sequence:
QQDVMARACLQKLKGTTELLPKRPQHLPGHPGWYRKLCPRLDDPAWTPGPSLLSLQMRVTPKLMALTWDGFPLHYSERHGWGYLVPGRRDNLAKLPTGTTLESAGVVCPYRAIESLYRKHCLEQGKQQLMPQEAGLAEEFLLTDNSAIWQTVEELDYLEVEAEAKMENLRAAVPGQPLALT
Uniprot:
P54098
Synonyms:
DNA polymerase subunit gamma-1;MDP1;MIRAS;mitochondrial DNA polymerase catalytic subunit;mitochondrial polymerase gamma catalytic subunit;MTDPS4A;MTDPS4B;PEO;PolG-alpha;POLG1;POLGA;polymerase (DNA directed), gamma;polymerase (DNA) gamma, catalytic subunit;SANDO;SCAE;truncated mitochondrial DNA polymerase gamma catalytic subunit;truncated mitochondrial polymerase gamma catalytic subunit
Extra Details:
Mitochondrial DNA polymerase is heterotrimeric, consisting of a homodimer of accessory subunits plus a catalytic subunit. The protein encoded by this gene is the catalytic subunit of mitochondrial DNA polymerase. The encoded protein contains a polyglutamine tract near its N-terminus that may be polymorphic. Defects in this gene are a cause of progressive external ophthalmoplegia with mitochondrial DNA deletions 1 (PEOA1), sensory ataxic neuropathy dysarthria and ophthalmoparesis (SANDO), Alpers-Huttenlocher syndrome (AHS), and mitochondrial neurogastrointestinal encephalopathy syndrome (MNGIE). Two transcript variants encoding the same protein have been found for this gene.
Shipping Conditions:
Blue Ice