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OM631985
Discount Price
OM631985-100ul
1~2 Week
100ul
OM631985-50ul
50ul
OM631985-20ul
20ul
1~2 Week
Product Profile
Product Name NU2M
Antibody Type Primary Antibodies
Product description catalytic activity:NADH + ubiquinone = NAD(+) + ubiquinol. disease:Defects in MT-ND2 are a cause of Leber hereditary optic neuropathy (LHON). LHON is a maternally inherited disease resulting in acute or subacute loss of central vision, due to optic nerve dysfunction. Cardiac conduction defects and neurological defects have also been described in some patients. LHON results from primary mitochondrial DNA mutations affecting the respiratory chain complexes. disease:Defects in MT-ND2 may be associated with mitochondrial susceptibility to Alzheimer disease (AD). Core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) that is believed to belong to the minimal assembly required for catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. Belongs to the complex I subunit 2 family.
Immunogen Synthesized peptide derived from human protein . at AA range: 40-120
Key Feature
Clonality Polyclonal
Isotype IgG
Host Species Rabbit
Tested Applications WB
WB:1:500-1:2000
Species Reactivity Human
Concentration 1mg/ml
Target Information
Molecular Weight(MW) 38 kDa
Database Links
SwissProt ID P03891
Positive Control Blood,Bone fossil,Bones,Breast cancer,Distant normal tissue,Glioma,Para-cancerous normal tissue,Pla
Application Notes WB:1:500-1:2000
Additional Information
Form Liquid
Storage Instructions Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. Avoid repeated freeze / thaw cycles.
Storage Buffer Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.
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