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NO66 Rabbit Polyclonal Antibody, 20ul Recombinant Protein disease:Defects in MT-ND2 are a
NO66 Rabbit Polyclonal Antibody, 20ul Recombinant Protein disease:Defects in MT-ND2 are a
NO66 Rabbit Polyclonal Antibody, 20ul Recombinant Protein disease:Defects in MT-ND2 are a
NO66 Rabbit Polyclonal Antibody, 20ul Recombinant Protein disease:Defects in MT-ND2 are a

NO66 Rabbit Polyclonal Antibody, 20ul Recombinant Protein disease:Defects in MT-ND2 are a

SKU: 54765343633

4.5
EUR111.00 EUR138.00

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NO66 Rabbit Polyclonal Antibody, 20ul Recombinant Protein disease:Defects in MT-ND2 are a

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Description

disease:Defects in MT-ND2 are a cause of Leber hereditary optic neuropathy (LHON)

which is an intracellular signaling domain that mediates protein-protein interactions between the Toll-like receptors(TLRs) and signal-transduction components

is an integral plasma membrane protein which binds melanin-concentrating hormone

Hearing impairment is a heterogeneous condition with over 40 loci described

This gene encodes a member of the NF-kappa-B inhibitor family| which contain multiple ankrin repeat domains

NO66 Rabbit Polyclonal Antibody, 20ul Recombinant Protein disease:Defects in MT-ND2 are a

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