Anti-SNX25 Antibody Picoband® fluoro594 Vervoeging

SNX25 (sorting nexin 25), also known as SBBI31 or MSTP043, is an 840 amino acid protein suggested to function in several stages of intracellular trafficking. A member of the sorting nexin family, SNX25 contains one PX (phox homology) domain, an RGS domain and one PXA domain. May be involved in several stages of intracellular trafficking.

SNX25

83891

Q9H3E2

Human, Mouse, Rat

E.coli-derived human SNX25 recombinant protein (Position: H48-K584) . Human SNX25 shares 86.4% amino acid (aa) sequence identity with mouse SNX25.

Flow Cytometry

Immunogen affinity purified.

Liquid

1. Chance, P. F., Rabin, B. A., Ryan, S. G., Ding, Y., Scavina, M., Crain, B., Griffin, J. W., Cornblath, D. R. Linkage of the gene for an autosomal dominant form of juvenile amyotrophic lateral sclerosis to chromosome 9q34. Am. J. Hum. Genet. 62: 633-640, 1998. 2. Dyck, P. J., Lambert, E. H. Lower motor and primary sensory neuron disease with peroneal muscular atrophy. II. Neurologic, genetic, and electrophysiologic findings in various neuronal degenerations. Arch. Neurol. 18: 619-625, 1968. 3. Gemignani, F., Guidetti, D., Bizzi, P., Preda, P., Cenacchi, G., Marbini, A. Peroneal muscular atrophy with hereditary spastic paraparesis (HMSN V) is pathologically heterogeneous: report of nerve biopsy in four cases and review of the literature. Acta Neuropath. 83: 196-201, 1992.

At -20 ̊C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

6

IgG

Each vial contains 50% glycerol, 0.9% NaCl, 0.2% Na2HPO4, 0.02% NaN3.