ALS2 (C-term) Rabbit Polyclonal Antibody
Other products for "ALS2"
Specifications
Product Data | |
Applications | WB |
Recommended Dilution | Western blot: 1:50 - 1:100. ELISA: 1:1,000. |
Reactivities | Human, Mouse |
Host | Rabbit |
Clonality | Polyclonal |
Immunogen | KLH conjugated synthetic peptide selected from the C-terminal region of human ALS2 |
Specificity | This antibody detects Alsin / ALS2 at C-term. |
Formulation | PBS with 0.09% (W/V) sodium azide State: Liquid Ig fraction |
Concentration | lot specific |
Purification | Prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS |
Storage | Store the antibody at 2 - 8 °C up to one month or (in aliquots) at -20 °C for longer. Avoid repeated freezing and thawing. |
Stability | Shelf life: one year from despatch. |
Gene Name | Homo sapiens ALS2, alsin Rho guanine nucleotide exchange factor (ALS2), transcript variant 2 |
Database Link | |
Background | ALS2 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 its gene result in several forms of juvenile lateral sclerosis and infantile-onset ascending spastic paralysis. |
Synonyms | ALS2CR6, KIAA1563 |
Note | Molecular weight: 183666 Da |
Reference Data | |
Protein Families | Druggable Genome |
Protein Pathways | Amyotrophic lateral sclerosis (ALS) |
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