Product Information
18737-1-AP targets ND4L in ELISA applications and shows reactivity with human, mouse samples.
| Tested Reactivity | human, mouse |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Peptide Predict reactive species |
| Full Name | NADH dehydrogenase, subunit 4L (complex I) |
| Calculated Molecular Weight | 11 kDa |
| GenBank Accession Number | P03901 |
| Gene Symbol | ND4L |
| Gene ID (NCBI) | 4539 |
| Conjugate | Unconjugated |
| Form | Liquid |
| Purification Method | Antigen affinity purification |
| Storage Buffer | PBS with 0.02% sodium azide and 50% glycerol , pH 7.3 |
| Storage Conditions | Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. 20ul sizes contain 0.1% BSA. |
Background Information
ND4L, also named as MTND4L and NADH4L, belongs to the complex I subunit 4L family. It is a 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. Mutation of ND4L will cause Leber hereditary optic neuropathy (LHON) which is a maternally inherited disease resulting in acute or subacute loss of central vision, due to optic nerve dysfunction.
