Catalog No.
YHF62901
Expression system
E. coli
Species
Homo sapiens (Human)
Protein length
Met1-His147
Predicted molecular weight
18.31 kDa
Nature
Recombinant
Endotoxin level
Please contact with the lab for this information.
Purity
>90% as determined by SDS-PAGE.
Accession
P68871
Applications
ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Form
Lyophilized
Storage buffer
Lyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1mM EDTA, 4% Trehalose, 1% Mannitol.
Reconstitution
Reconstitute in sterile water for a stock solution. A copy of datasheet will be provided with the products, please refer to it for details.
Shipping
In general, proteins are provided as lyophilized powder/frozen liquid. They are shipped out with dry ice/blue ice unless customers require otherwise.
Stability and Storage
Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.
Alternative Names
Hemoglobin subunit beta, HBB, Beta-globin, Hemoglobin beta chain
Cigarette Smoke-Induced PPAR Signaling Dysregulation Accelerates Alzheimer's Disease Pathogenesis and Cognitive Decline in 5xFAD Mice., PMID:40513939
Screening and identification of novel protein markers of early-stage lung cancer and construction and application of screening models., PMID:40496615
PDE3B and HBB are key prognostic biomarkers driving cell proliferation and regulating immune microenvironment in breast cancer., PMID:40462176
A comprehensive, multi-center, immunogenomic analysis of melanoma brain metastases., PMID:40457397
Generation of integration-free induced pluripotent stem cell (iPSC) line MURAi002-A from hemoglobin E/β-thalassemia disease patient harboring βE/β0 (CD41/42, -CTTT) compound heterozygous mutation., PMID:40441082
Hb Lepore Rochester-MN, a novel βδβ double crossover hemoglobin variant., PMID:40413840
Splenic comparative transcriptome analysis reveals the immunological mode of undomesticated Gayal (Bos frontalis) for adapting to harsh environments., PMID:40394466
Investigate the Effect of ZFP64 on mRNA Expression of HBG Based on Bioinformatics and Experimental Validation., PMID:40392482
Genetic polymorphism of novel SNP rs5006884 in OR51B6 and SNP rs4499252 in AHSP among transfusion-dependent and non-transfusion-dependent β-thalassemia/Hb E patients in Thailand: a multivariate analysis of clinical and genetic polymorphism., PMID:40377674
Crosstalk Between Sickle Cell Disease and Ferroptosis., PMID:40332185
[Serum proteomics and machine learning unveil new diagnostic biomarkers for tuberculosis in adolescents and young adults]., PMID:40328710
Kompetitive allele specific PCR (KASP) based genotyping of sickle gene in the selected sub-ethnic tribal population of Gujarat and Madhya Pradesh., PMID:40314324
Antioxidant Activity and Chemical Alterations of Honeybee Brood Bio-Peptides Interacting with Honey Under Moist-Dried Thermal Aging., PMID:40227234
Generation of an integration-free induced pluripotent stem cell line, MURAi006-A, from a hemoglobin E/β-thalassemia patient harboring the βE/β0 (Codon 17, A > T) compound heterozygous mutation., PMID:40179812
Genome editing strategies for targeted correction of β-globin mutation in sickle cell disease: From bench to bedside., PMID:40165374
Molecular Characterization of Complex Thalassemia with Multiple Variants in β-Globin Gene Cluster and the Identification of a Novel Structural Rearrangement in γ-Globin Gene., PMID:40140352
SunTag-PE: a modular prime editing system enables versatile and efficient genome editing., PMID:40097588
Genetic architecture of the red blood cell proteome in genetically diverse mice reveals central role of hemoglobin beta cysteine redox status in maintaining circulating glutathione pools., PMID:40093052
Interrogating mediators of single-cell transcriptional changes in the acute damaged cerebral cortex: Insights into endothelial-astrocyte interactions., PMID:40090391
Subepicardial adipose genes contribute to the deterioration of heart failure preserved ejection fraction., PMID:40060963
Newborn Screening for Sickle Cell Disease and Thalassemia., PMID:40053336
Hereditary Angioedema with Normal C1 Inhibitor: an Updated International Consensus Paper on Diagnosis, Pathophysiology, and Treatment., PMID:40053270
Decoding Allergenicity Modulation in Cold Argon Plasma-Treated Casein: A Multi-Omics Exploration., PMID:40048467
Knowledge about globin genetics for precision diagnosis of hemoglobinopathies: A case Study., PMID:40023305
A differentiated β-globin gene replacement strategy uses heterologous introns to restore physiological expression., PMID:40022449
Combined heterozygosity for hemoglobin Paksé, α-thalassemia and for hemoglobin E, β- thalassemia ̵ first appearance in Europe., PMID:40016398
Long-range enhancer-controlled genes are hypersensitive to regulatory factor perturbations., PMID:40010352
Analysis of genotypic distribution and rare variants of patients with α/β-thalassemia screened in one hospital in Beijing, China., PMID:39985037
Type 2 immunity in allergic diseases., PMID:39962262
Bidirectional Mendelian Randomization identifies plasma proteins associated with urticaria risk., PMID:39961865
Metabolic and Proteomic Divergence is Present in Spleens and Livers from Berkeley Sickle Cell Anemia and β-Thalassemia Mice., PMID:39947632
Transcriptomic signatures of severe acute mountain sickness during rapid ascent to 4,300 m., PMID:39944919
Plasma proteome fingerprint in kidney diseases., PMID:39896931
A replication study of novel fetal hemoglobin-associated genetic variants in sickle cell disease-only cohorts., PMID:39886999
A next-generation sequencing-based universal target panel and algorithm for one-stop detection of copy number alterations and single-nucleotide variations in the HBB gene cluster for rapid diagnosis of β-thalassemia., PMID:39820710
Enhancing Thalassemia Diagnosis: Advantages of Third-Generation Sequencing., PMID:39808152
A Rare Hemoglobin Variant: Hemoglobin G-Siriraj, in a Moroccan Patient., PMID:39808144
Identification of a β-Globin Gene Mutation with the Genotype β-28(A > G), IVS-I-5(G > A)/βCD 71/72(+A) Using Third-Generation Sequencing., PMID:39780430
Dysregulation of Nitrosylation Dynamics Promotes Nitrosative Stress and Contributes to Cardiometabolic Heart Failure with Preserved Ejection Fraction., PMID:39763741
Transamniotic Delivery of Hematopoietic Stem Cells Genetically Modified to Carry a Human Hemoglobin Subunit Beta Gene (HBB) in a Healthy Rodent Model., PMID:39743433
First clinical and pedigree study of rare HBB: c.316-90 A > G variant in β-globin gene in Chinese population using third-generation sequencing., PMID:39738591
Hemoglobin-derived amyloid fibrils: Fibrillization mechanisms and potential applications., PMID:39736176
Molecular Characterization of δβ Thalassemia/Hereditary Persistence of Fetal Hemoglobin and Its Correlation With Clinical and Hematological Profile; a Single Center Study in North India., PMID:39731309
Hb Monza: A novel extensive HBB duplication with preserved α-β subunit interaction and unstable hemoglobin phenotype., PMID:39701095
Abnormal High HbA1c Caused by Hb Takasago Variant Firstly in a Chinese Pedigree., PMID:39662011
Molecular Identification and the Hematological Findings of Four Novel Variants in Globin Genes in Jiangxi Province of Southern China., PMID:39659024
Ocrelizumab in Early-Stage Relapsing-Remitting Multiple Sclerosis: The Phase IIIb ENSEMBLE 4-Year, Single-Arm, Open-Label Trial., PMID:39626127
The genotype and phenotype analysis in 3 cases with the rare genotype of HBB:c.316-146T > G., PMID:39585810
Single-stranded DNA with internal base modifications mediates highly efficient knock-in in primary cells using CRISPR-Cas9., PMID:39569586
For research use only. Not for human or drug use.
