Recombinant Cynomolgus ARSE Protein, His-tagged
Cat.No. : | ARSE-313C |
Product Overview : | Recombinant Cynomolgus ARSE full length or partial length protein was expressed. |
- Specification
- Gene Information
- Related Products
Source : | Mammalian Cells |
Species : | Cynomolgus |
Tag : | His |
Form : | Liquid or lyophilized powder |
Endotoxin : | < 1.0 EU per μg of the protein as determined by the LAL method. |
Purity : | >80% |
Notes : | This item requires custom production and lead time is between 5-9 weeks. We can custom produce according to your specifications. |
Storage : | Store it at +4 ºC for short term. For long term storage, store it at -20 ºC~-80 ºC. |
Storage Buffer : | PBS buffer |
Gene Name : | ARSE arylsulfatase E [ Macaca fascicularis (crab-eating macaque) ] |
Official Symbol : | ARSE |
Synonyms : | ARSE; ASE; |
Gene ID : | 102138132 |
mRNA Refseq : | NM_001283217 |
Protein Refseq : | NP_001270146 |
MIM : | |
UniProt ID : | Q60HH5 |
Products Types
◆ Recombinant Protein | ||
ARSE-2824H | Recombinant Human ARSE Protein, MYC/DDK-tagged | +Inquiry |
ARSE-63C | Recombinant Cynomolgus Monkey ARSE Protein, His (Fc)-Avi-tagged | +Inquiry |
ARSE-863H | Recombinant Human ARSE protein, GST-tagged | +Inquiry |
ARSE-3661H | Recombinant Human ARSE, His-tagged | +Inquiry |
◆ Lysates | ||
ARSE-38HCL | Recombinant Human ARSE lysate | +Inquiry |
Related Gene
For Research Use Only. Not intended for any clinical use. No products from Creative BioMart may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative BioMart.
Inquiry
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Q&As (7)
Ask a questionCurrently, there is no cure for X-linked chondrodysplasia punctata (CDPX1). Treatment focuses on managing the symptoms and providing supportive care. Physical therapy, medications, and surgical interventions may be recommended based on individual needs and associated complications.
Mutations in the ARSE gene can lead to a deficiency or reduced activity of the ARSE enzyme. This can result in a rare genetic disorder known as X-linked chondrodysplasia punctata (CDPX1), which primarily affects skeletal development and can manifest with characteristic bone and cartilage abnormalities.
X-linked chondrodysplasia punctata (CDPX1) is inherited in an X-linked recessive manner. This means that the condition primarily affects males, who have one X chromosome, while females can be carriers of the disease unless both their X chromosomes are affected.
Yes, variations or mutations in the ARSE protein can impact its catalytic efficiency. Certain mutations may reduce or abolish the enzymatic activity of ARSE, resulting in a deficiency of the enzyme and impaired breakdown of sulfated GAGs.
Yes, genetic counseling can be highly beneficial for families with X-linked chondrodysplasia punctata (CDPX1) or ARSE gene mutations. Genetic counselors can provide information about the condition, inheritance patterns, prenatal testing options, and available support resources. They can also help families understand the risk of passing on the mutation and make informed decisions regarding family planning.
Yes, X-linked chondrodysplasia punctata (CDPX1) is the main disorder associated with mutations in the ARSE gene. It is characterized by skeletal abnormalities, developmental delays, characteristic facial features, and other symptoms that can vary in severity.
The activity of the ARSE protein can be regulated through various mechanisms. One such mechanism is the presence of specific cofactors or activators that can enhance ARSE activity. Additionally, the expression of the ARSE gene itself can be controlled by genetic and epigenetic factors.
Customer Reviews (3)
Write a reviewThe ARSE protein is highly recommended for its exceptional performance in ELISA assays.
The bands of proteins in Western Blotting experiments were very clear.
The ARSE protein's excellent performance in ELISA ensures accurate and reproducible results, enhancing the reliability of experimental data.
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