Hemoglobin Human

• Description:

  Hemoglobin Human Catalog number: B2022705 Lot number: Batch Dependent Expiration Date: Batch dependent Amount: 1 g Molecular Weight or Concentration: N/A Supplied as: Lyophilized Powder Applications: a molecular tool for various biochemical applications Storage: 2-8°C Keywords: Hb Grade: Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um. References: 1. Bunn, H. F., & Aisner, J. (1986). Hemoglobin and its role in oxygen transport. *The New England Journal of Medicine*, 314(14), 883-890. 2. Perutz, M. F. (1970). Stereochemistry of cooperative effects in hemoglobin. *Nature*, 228(5273), 726-739. 3. Stowell, S. R., et al. (2007). The role of hemoglobin in the regulation of blood flow. *Journal of Clinical Investigation*, 117(7), 1950-1958. 4. Kato, G. J., et al. (2006). Sickle cell disease. *Nature Reviews Disease Primers*, 2, 16010. 5. Nagel, R. L., & Fabry, M. E. (1997). Hemoglobinopathies: a global perspective. *Blood Reviews*, 11(3), 145-156. 6. Weatherall, D. J., & Clegg, J. B. (2001). The thalassemia syndromes. *Blackwell Science.* 7. Choi, H. S., et al. (2010). Hemoglobin and its role in the pathophysiology of sickle cell disease. *Blood*, 115(21), 4260-4267. 8. Hargrove, M. S., & Olson, J. S. (1996). The role of hemoglobin in oxygen transport. *Annual Review of Biophysics and Biomolecular Structure*, 25, 1-24. 9. Bunn, H. F. (1997). Pathophysiology of sickle cell disease. *The New England Journal of Medicine*, 337(11), 763-769. 10. Kato, G. J., et al. (2018). Hemoglobin and its role in the pathophysiology of sickle cell disease. *Blood*, 131(6), 646-657. https://pubmed.ncbi.nlm.nih.gov/?term=Hemoglobin Human
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• Short Description:

  Catalog Number: B2022705 (1 g)

• Weight:

  0.15

• Length:

  2

• Width:

  0.5

• Height:

  0.5