Recombinant Cynomolgus Monkey ASAH1 Protein, His (Fc)-Avi-tagged

• Cat.No.: ASAH1-65C
• Product Overview: Recombinant Cynomolgus Monkey ASAH1 with His (Fc)-Avi tag was expressed and purified

Specification

• Source: HEK293
• Species: Cynomolgus Monkey
• Tag: His (Fc)-Avi
• Endotoxin: < 1.0 EU per μg of the protein as determined by the LAL method
• Purity: ≥85% by SDS-PAGE
• Stability: Stable for at least 6 months from the date of receipt of the product under proper storage and handling conditions. Avoid repeated freeze-thaw cycles.
• Storage: For long term storage, aliquot and store at -20 to -80 centigrade. Avoid repeated freezing and thawing cycles.
• Storage Buffer: PBS buffer

Gene Information

• Gene Name: ASAH1 N-acylsphingosine amidohydrolase (acid ceramidase) 1 [ Macaca fascicularis (crab-eating macaque) ]
• Official Symbol: ASAH1
• Synonyms: ASAH1; AC; ACDase; Acid CDase; Acylsphingosine deacylase
• Gene ID: 102118393
• mRNA Refseq: NM_001285344
• Protein Refseq: NP_001272273
• UniProt ID: I7GEN4

Reviews

03/21/2022

Such dedicated support makes me feel confident in my choice of using the ASAH1 protein for my experiments.

04/09/2017

The manufacturer's commitment to excellence is truly commendable, especially when it comes to their outstanding technical support.

11/02/2016

The ASAH1 Protein is a protein of exceptional quality that surpasses my expectations and fulfills all my experimental requirements.

Q&As

Can ASAH1 activity be targeted for therapeutic interventions?

Given the involvement of ASAH1 in various diseases, including cancer, modulating its activity or developing ASAH1 inhibitors holds promise as potential therapeutic strategies.

Can alterations in ASAH1 gene expression affect cellular differentiation?

Yes, alterations in ASAH1 gene expression or activity can impact cellular differentiation processes, as ceramide metabolism is crucial for normal development and tissue homeostasis.

Are there any diseases or conditions associated with the ASAH1 protein?

Yes, mutations or deficiencies in the ASAH1 gene are associated with Farber disease, a rare inherited disorder characterized by the accumulation of ceramide in tissues throughout the body.

Can ASAH1 deficiency be prevented?

ASAH1 deficiency, as seen in Farber disease, is a genetic disorder. Prevention involves genetic counseling for at-risk individuals and prenatal testing during pregnancy.

Can ASAH1 deficiency be detected in newborn screening tests?

Currently, ASAH1 deficiency is not included in routine newborn screening panels. However, advancements in testing methods may lead to its inclusion in the future.

Does the ASAH1 protein have any other biological functions?

Besides its role in ceramide metabolism, the ASAH1 protein can affect immune response, inflammation, and cellular stress responses.

How does dysfunction of the ASAH1 protein impact ceramide metabolism?

Dysfunction of the ASAH1 protein impairs the breakdown of ceramide, leading to its accumulation in various tissues and disrupting cellular homeostasis.

Is the ASAH1 protein involved in any signaling pathways?

Yes, the ASAH1 protein can modulate signaling pathways like the sphingosine-1-phosphate pathway, which influences various cellular processes such as migration, inflammation, and angiogenesis.