Recombinant Rhesus monkey CTSA Protein, His-tagged
Cat.No. : | CTSA-1085R |
Product Overview : | Recombinant Rhesus monkey CTSA full length or partial length protein was expressed. |
- Specification
- Gene Information
- Related Products
Source : | Mammalian Cells |
Species : | Rhesus monkey |
Tag : | His |
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 : | CTSA cathepsin A [ Macaca mulatta (Rhesus monkey) ] |
Official Symbol : | CTSA |
Synonyms : | CTSA; PPGB; lysosomal protective protein; protective protein for beta-galactosidase; |
Gene ID : | 708592 |
mRNA Refseq : | NM_001266851 |
Protein Refseq : | NP_001253780 |
MIM : | |
UniProt ID : | F7G1E1 |
Products Types
◆ Recombinant Protein | ||
CTSA-3374H | Recombinant Human CTSA Protein, MYC/DDK-tagged | +Inquiry |
Ctsa-908M | Recombinant Mouse Ctsa protein(Met1-Tyr474), His-tagged | +Inquiry |
CTSA-895H | Recombinant Human CTSA protein(Met1-Tyr480), His-tagged | +Inquiry |
Ctsa-2366M | Recombinant Mouse Ctsa Protein, Myc/DDK-tagged | +Inquiry |
CTSA-910R | Recombinant Rhesus Macaque CTSA Protein, His (Fc)-Avi-tagged | +Inquiry |
◆ Lysates | ||
CTSA-3026HCL | Recombinant Human CTSA cell lysate | +Inquiry |
CTSA-2399MCL | Recombinant Mouse CTSA cell 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.
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Q&As (7)
Ask a questionPost-translational modifications of CTSA are not well-documented, requiring further research for comprehensive understanding.
CTSA has roles in various cellular processes outside the lysosome, though these are less well understood compared to its lysosomal functions.
CTSA is crucial for the catabolism of glycoproteins, aiding in the removal of terminal sugar moieties.
Therapeutic strategies for CTSA-related disorders are in the early stages of development, with enzyme replacement therapy being a potential avenue.
Dysfunction or deficiency in CTSA leads to Galactosialidosis, characterized by the accumulation of sialyloligosaccharides and glycoproteins in tissues.
It forms a complex with β-galactosidase and neuraminidase, preventing their premature degradation and facilitating their activation.
CTSA acts as a protective protein, ensuring the stability and proper function of other lysosomal enzymes.
Customer Reviews (3)
Write a reviewProduct arrived quickly, undamaged.
Great results, worth buying.
Highly pure, excellent product.
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