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ALS2 / Alsin

amyotrophic lateral sclerosis 2 (juvenile)

ALS2 / Alsin contains an ATS1/RCC1-like domain, a RhoGEF domain, and a vacuolar protein sorting 9 (VPS9) domain, all of which are guanine-nucleotide exchange factors that activate members of the Ras superfamily of GTPases. The protein functions as a guanine nucleotide exchange factor for the small GTPase RAB5. The protein localizes with RAB5 on early endosomal compartments, and functions as a modulator for endosomal dynamics. Mutations in this gene result in several forms of juvenile lateral sclerosis and infantile-onset ascending spastic paralysis. Multiple transcript variants encoding different isoforms have been found for this gene.

Gene Name: amyotrophic lateral sclerosis 2 (juvenile)
Synonyms: ALS2, ALS2CR6, ALSJ, IAHSP, Alsin, PLSJ, KIAA1563
Target Sequences: NM_020919 NP_065970.2 Q96Q42

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Proteins (2)
Recombinant (2)
ALS2 / Alsin (2)
No (2)
GST, N-terminus (1)
His, N-Terminal (1)
Human (2)
E. coli (1)
Wheat Germ Extract (1)
ALS2 / Alsin Protein - 12.5% SDS-PAGE Stained with Coomassie Blue.
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Wheat Germ Extract
GST, N-terminus
10 µg/$479; 25 µg/$670
ALS2 / Alsin Protein
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E. coli
His, N-Terminal
42.4 kDa
50 µg/$419
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If you do not find the reagent or information you require, please contact Customer.Support@LSBio.com to inquire about additional products in development.

PLEASE NOTE

For RESEARCH USE ONLY. Intended for use by laboratory professionals. Not intended for human diagnostic or therapeutic purposes.

The data on this page has been compiled from LifeSpan internal sources, the National Center for Biotechnology Information (NCBI), and The Universal Protein Resource (UniProt).