Analytical Data
-
Gene name
RPS26
- Application
-
Alternative Names
40S ribosomal protein S26; Ribosomal protein S26; RPS26; RS26_HUMAN
-
Species
Human
-
Source
E. coli
-
Tag
His tag N-Terminus
-
Purity
Greater than 90% as determined by SDS-PAGE.
-
Uniprot
P62854
-
Expression Region
2-115 aa
-
AA Sequence
TKKRRNNGR AKKGRGHVQP IRCTNCARCV PKDKAIKKFV IRNIVEAAAV RDISEASVFD AYVLPKLYVK LHYCVSCAIH SKVVRNRSRE ARKDRTPPPR FRPAGAAPRP PPKPM
-
Molecular Weight
13.0 kDa
-
Endotoxin
< 1.0 EU per μg protein as determined by the LAL method.
-
Form
Freeze-dried powder
-
Buffer formulation
PBS, pH7.4, containing 0.01% SKL, 1mM DTT, 5% Trehalose and Proclin300.
-
Reconstitution
Reconstitute in ddH2O to a concentration of 0.1-0.5 mg/mL. Do not vortex.
- Customization
-
Stability Test
The thermal stability is described by the loss rate. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37℃ for 48h, and no obvious degradation and precipitation were observed. The loss rate isless than 8% within the expiration date under appropriate storage condition.
-
Storage & Shelf Life
Samples are stable for up to twelve months from date of receipt at -20℃ to -80℃. Store it under sterile conditions at -20℃ to -80℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
-
Shipping
In general, recombinant proteins are supplied as lyophilized powder and shipped at ambient temperature. For bulk packages, the proteins are provided as frozen liquid and shipped with blue ice, unless otherwise requested by the customer.
Quality inspection process
Related Products
Protein Description
RPS26, a member of the ribosomal protein family, plays a crucial role in ribosome biogenesis and protein synthesis. Research into RPS26 has gained momentum due to its involvement in various cellular processes and its implications in certain diseases, particularly in cancer and Diamond-Blackfan anemia, a rare hereditary blood disorder characterized by ineffective erythropoiesis. Mutations and dysregulation of RPS26 can lead to impaired ribosome function, which ultimately affects protein production and cellular homeostasis. The study of recombinant RPS26 protein has become essential for understanding its structural and functional properties, as well as its interactions within the ribosomal machinery. By producing RPS26 in a recombinant form, researchers can investigate its biochemical interactions, potential post-translational modifications, and its role in the assembly and stabilization of ribosomal subunits. Furthermore, exploring the mechanisms by which RPS26 contributes to disease phenotypes can reveal novel therapeutic targets and strategies for treating conditions associated with ribosomal dysfunction. Overall, the study of RPS26 as a recombinant protein serves as a vital tool in elucidating its biological significance and the molecular underpinnings of diseases linked to ribosomal anomalies.











