Anti-SNX25 Antibody Picoband® Fluoro647 Conjugated

Product Specifications

Background

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.

Gene Name

SNX25

Gene ID

83891

UniProt

Q9H3E2

Host

Rabbit

Reactivity

Human, Mouse, Rat

Immunogen

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

Clonality

Polyclonal

Applications

Flow Cytometry

Purification

Immunogen affinity purified.

Form

Liquid

References & Citations

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.