Recombinant Mouse Hbb protein, His & S-tagged
Cat.No. : | Hbb-7866M |
Product Overview : | Recombinant Mouse Hbb aa. (Met1~His147 (Accession # P02088)) fused with N-terminal His & S tag was produced in E. coli cells. |
- Specification
- Gene Information
- Related Products
Source : | E. coli |
Species : | Mouse |
Tag : | His & S |
Form : | Freeze-dried powder |
Molecular Mass : | Predicted Molecular Mass: 21.5kDa |
Protein length : | Met1~His147 (Accession # P02088) |
Endotoxin : | <1.0EU per 1ug (determined by the LAL method) |
Purity : | >95% |
Characteristic : | The isoelectric point is 6.3. |
Applications : | SDS-PAGE; WB; ELISA; IP |
Stability : | The thermal stability is described by the loss rate of the target protein. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37°C for 48h, and no obvious degradation and precipitation were observed. (Referring from China Biological Products Standard, which was calculated by the Arrhenius equation.) The loss of this protein is less than 5% within the expiration date under appropriate storage condition. |
Storage : | Avoid repeated freeze/thaw cycles. Store at 2-8°C for one month. Aliquot and store at -80°C for 12 months. |
Storage Buffer : | Supplied as lyophilized form in PBS, pH7.4, containing 1mM DTT, 5% trehalose, 0.05% sarcosyl and preservative. |
Reconstitution : | Reconstitute in sterile PBS, pH7.2-pH7.4. |
Gene Name : | Hbb hemoglobin beta chain complex [ Mus musculus (house mouse) ] |
Official Symbol : | Hbb |
Synonyms : | Hbb; hemoglobin beta chain complex; |
Gene ID : | 15127 |
UniProt ID : | P02088 |
Products Types
◆ Native Protein | ||
HBB-001H | Native Human Hemoglobin S, Ferrous Stabilized | +Inquiry |
HBb-49S | Native Sheep Hemoglobin Beta (HBb) Protein | +Inquiry |
◆ Lysates | ||
HBB-5622HCL | Recombinant Human HBB 293 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 questionHBB, part of the hemoglobin molecule, is crucial for oxygen transport in the blood.
Therapies targeting HBB mutations aim to correct or compensate for the defective hemoglobin in blood disorders.
HBB mutations can lead to abnormal hemoglobin, resulting in impaired oxygen transport and cell damage.
It forms part of hemoglobin's structure, binding oxygen in red blood cells.
Altered HBB expression affects hemoglobin's efficiency, impacting oxygen delivery and health.
HBB interacts with other hemoglobin subunits to form a functional oxygen-carrying complex.
Mutations in HBB cause sickle cell anemia and thalassemia, affecting hemoglobin's function.
Customer Reviews (3)
Write a reviewHelps us reach milestones. Efficient and accurate service.
Critical for success. Trusted for precise protein analysis.
Supports groundbreaking discoveries. Highly recommended for research.
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