A18138
Size
  • 50ul
  • 100ul
Price
  • $129
  • $229
Qty
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Product description

catalytic activity:NADH + ubiquinone = NAD(+) + ubiquinol.,disease:Defects in MT-ND1 are a cause of Leber hereditary optic neuropathy (LHON) [MIM:535000]. LHON is a maternally inherited disease resulting in acute or subacute loss of central vision, due to

Source
Rabbit
Applications
WB,IHC,ELISA
Reactivity
Human
Dilution
WB: 1/500 - 1/2000. IHC: 1/100 - 1/300. ELISA: 1/40000. Not yet tested in other applications.
Storage
-20°C/1 year
Specificity
ND1 Polyclonal Antibody detects endogenous levels of ND1 protein.
Source/Purification
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Immunogen
The antiserum was produced against synthesized peptide derived from human MT-ND1. AA range:176-225
Uniprot No
P03886
Alternative names
MT-ND1; MTND1; NADH1; ND1; NADH-ubiquinone oxidoreductase chain 1; NADH dehydrogenase subunit 1
Form
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Clonality
Polyclonal
Background
catalytic activity:NADH + ubiquinone = NAD(+) + ubiquinol.,disease:Defects in MT-ND1 are a cause of Leber hereditary optic neuropathy (LHON) [MIM:535000]. LHON is a maternally inherited disease resulting in acute or subacute loss of central vision, due to
Other
Gene_name: MT-ND1 ; Protein_name: NADH-ubiquinone oxidoreductase chain 1; Expression: Blood,Bone fossil,Bones,Breast cancer,Distant normal tissue,Glioma,
Mol.Wt (Da)
36 kD
Concentration
1 mg/ml

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