SPG7 (NM 003119) Humaan Recombinant eiwit

This gene encodes a mitochondrial metalloprotease protein that is a member of the AAA family. Members of this protein family share an ATPase domain and have roles in diverse cellular processes including membrane trafficking, intracellular motility, organelle biogenesis, protein folding, and proteolysis. Mutations in this gene cause autosomal recessive spastic paraplegia 7. Two transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Mar 2014]

Purified recombinant protein of Human spastic paraplegia 7 (pure and complicated autosomal recessive) (SPG7), nuclear gene encoding mitochondrial protein, transcript variant 1, Gly300-Phe573, with N-terminal His tag, expressed in E. coli, 50ug

CAR; CMAR; PGN; SPG5C

6687

Q9UQ90

NM_003119

16q24.3

E. coli

N-His

>50 ug/mL as determined by microplate BCA method

> 80% as determined by SDS-PAGE and Coomassie blue staining

Liquid

50mM Tris, 8M Urea, pH8.0

Protease, Transmembrane

29.8 kDa

Stable for 1 year at -20°C or below from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. For long-term storage, aliquot and store at -20°C or below. Avoid repeated freeze-thaw cycles.

SPG7

Human

NP_003110

https://www.ncbi.nlm.nih.gov/gene/6687

https://www.uniprot.org/uniprot/Q9UQ90

https://www.ncbi.nlm.nih.gov/nuccore/NM_003119

https://www.ncbi.nlm.nih.gov/nuccore/NP_003110