Abcam, ab316195, Anti-Als2 antibody [EPR27469-29]

Size: 10µL-TRIAL / 20µL / 100µL / 1mL
Rabbit Recombinant Monoclonal ALS2 antibody. Suitable for WB, IHC-P and reacts with Mouse samples.
Key facts
Host species:Rabbit,
Clonality:Monoclonal,
Clone number:EPR27469-29,
Isotype:IgG,
Carrier free:No,
Reacts with:Mouse,
Applications:WB, IHC-PSee reactivity dataSee the reactivity data table below for information on validated species and application combinations.,
Immunogen:The exact immunogen used to generate this antibody is proprietary information.

Product details:
Patented technology
Our RabMAb
technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to
RabMAb® patents
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- High batch-to-batch consistency and reproducibility
- Improved sensitivity and specificity
- Long-term security of supply
- Animal-free batch production
For more information, read more on
recombinant antibodies

Properties and Storage Information:
Form-Liquid, Purification technique-Affinity purification Protein A, Storage buffer-pH: 7.2 - 7.4Preservative: 0.01% Sodium azideConstituents: PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA, Shipped at conditions-Blue Ice, Appropriate short-term storage duration-1-2 weeks, Appropriate short-term storage conditions-+4°C, Appropriate long-term storage conditions--20°C, Aliquoting information-Upon delivery aliquot, Storage information-Avoid freeze / thaw cycle

Supplementary Information:
This supplementary information is collated from multiple sources and compiled automatically.
Als2 also known as ALS2 or Alsin is a protein implicated in intracellular trafficking. It contains a massive molecular size of approximately 184 kDa. Als2 exhibits multiple domains such as the VPS9 Dbl/CDC24 and ALS2CR domain which facilitate its role in regulating endosome dynamics. This protein expresses strongly in the nervous system especially within motor neurons and is also found in other tissues like the liver. Though Als2 functions largely within cellular compartments its presence in the central nervous system suggests a significant neural relevance.
Biological function summary
Als2 plays an important role in neuronal survival and function. It operates as part of a molecular complex involved in endosomal trafficking and membrane exchange. Als2 interacts with Rab5 a small GTPase facilitating early endosome membrane fusion. By acting on cellular vesicle pathways Als2 contributes critically to maintaining cellular homeostasis and membrane turnover in neuronal cells thereby supporting nervous system integrity.
Pathways
Als2 is essential in endocytic pathways and the regulation of synaptic vesicle cycling. Within these pathways Als2 interacts closely with other proteins such as Rab5 and Rac1 influencing cellular processes like endosome fusion and actin cytoskeleton remodeling. This interaction highlights its participation in organizing intracellular vesicle transport and contributing to the maintenance of synaptic function.
Als2 has a direct association with neurodegenerative conditions particularly amyotrophic lateral sclerosis (ALS) and infantile-onset ascending hereditary spastic paralysis (IAHSP). Mutations in the Als2 gene disrupt normal protein function contributing to motor neuron degeneration and neuronal dysfunction. This relationship with neurodegenerative diseases highlights Als2's importance in motor neuron vitality. Additionally Als2 connects to other proteins such as SOD1 and TDP-43 in these conditions linking it to broader pathways implicated in disease mechanisms.