Human OPA1 protein
Recombinant protein from the full-length sequence of homo sapiens OPA1, mitochondrial dynamin like GTPase (OPA1), transcript variant 3 (NM_130832), with a DYKDDDDK tag.
BERHS; largeG; MGM1; MTDPS14; NPG; NTG
>90% by SDS-PAGE gel and Coomassie Blue staining
Antigens, Western, ELISA and other in vitro binding or in vivo functional assays, and protein-protein interaction studies; For research & development use only!
Purified protein formulated in a sterile solution of TBS buffer, pH7.4, without any preservatives
Endotoxin level is < 0.1 ng/µg of protein (<1EU /µg)
This gene product is a nuclear-encoded mitochondrial protein with similarity to dynamin-related GTPases. It is a component of the mitochondrial network. Mutations in this gene have been associated with optic atrophy type 1, which is a dominantly inherited optic neuropathy resulting in progressive loss of visual acuity, leading in many cases to legal blindness. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009].
There's no citations at this moment.
There's no FAQs at this moment.
There's no reviews at this moment.