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| Cat.No | ACP08490 | Target Name | TMEM126A |
|---|---|---|---|
| Target Synonyms | TMEM126A; Transmembrane protein 126A | Form | Lyophilized powder |
| Expression System | Custom Production. Please inquire and provide the desire expression system. | Protein Length | Partial |
| Purity | >85% (SDS-PAGE) | Storage Buffer | 5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0. |
| Target Species | Human | Uniprot ID | Q9H061 |
|---|
Uniprot Id
Q9H061
Target Species
Human
Target Name
TMEM126A
Target Full Name
Transmembrane protein 126A
Target Involvement
Optic atrophy 7 with or without auditory neuropathy (OPA7)
Target Subcellular Location
Mitochondrion inner membrane; Multi-pass membrane protein.
Target Protein Families
TMEM126 family
Target Tissue Specificity
Strongly expressed in brain, cerebellum, skeletal muscle, testis. High expression also found in fetal brain, fetal retinal pigmentary epithelium, and fetal retina. Highly expressed in retinal ganglion cells.
Target Synonyms
TMEM126A; Transmembrane protein 126A
Target Background
The protein encoded by this gene is a mitochondrial membrane protein of unknown function. Defects in this gene are a cause of optic atrophy type 7 (OPA7). Two transcript variants encoding different isoforms have been found for this gene.
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