SPG7 Antilichaam

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.

6687

Q9UQ90

Human, Mouse, Rat

Recombinant fusion protein containing a sequence corresponding to amino acids 1-250 of human SPG7 (NP_003110.1) .

Unconjugated

Primary Antibodies

Cell Cycle, Neuroscience

Affinity purification

U-87MG

Batch dependent

PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

None

Blue Ice

Store at -20˚ C. Avoid freeze / thaw cycles.

Observed: 88kDa

IgG

SPG7

MCF7

HT-29

K-562

Mouse brain

Mouse kidney

Paraplegin

Homo sapiens

Paraplegin, 3424-, Spastic paraplegia 7 protein, SPG7, CAR, CMAR, PGN

WB, IHC

Liquid