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  2. Polyclonal

GTX100398

DNA polymerase gamma antibody

Cannot supply to this region.

SKU:
GTX100398
Additional Names:
DNA polymerase gamma, catalytic subunit , MDP1 , MIRAS , MTDPS4A , MTDPS4B , PEO , POLG1 , POLGA , SANDO , SCAE
Application:
WB, IHC-P, IF, ICC, IP
Concentration:
0.67 mg/ml
Physical State:
Liquid
Species Reactivity:
Human
Purification:
Affinity Purified
Storage Conditions:
-20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
Supplier:
Genetex
Host:
Rabbit
Reactivities:
Human, Rat
Buffer:
PBS, 20% Glycerol, 0.025% ProClin 300.
Immunogen:
Recombinant protein encompassing a sequence within the C-terminus region of human DNA polymerase gamma. The exact sequence is proprietary.
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. [provided by RefSeq]
Shipping Conditions:
Blue Ice