Recombinant Rhesus monkey HBB Protein, His-tagged
Cat.No. : | HBB-2041R |
Product Overview : | Recombinant Rhesus monkey HBB 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 : | HBB hemoglobin, beta [ Macaca mulatta (Rhesus monkey) ] |
Official Symbol : | HBB |
Synonyms : | HBB; hemoglobin subunit beta; globin, beta; |
Gene ID : | 715559 |
mRNA Refseq : | NM_001164428 |
Protein Refseq : | NP_001157900 |
MIM : | |
UniProt ID : | C6KGT1 |
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.
Inquiry
- Q&As
- Reviews
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.
Ask a Question for All HBB Products
Required fields are marked with *
My Review for All HBB Products
Required fields are marked with *
Inquiry Basket