HSA Protein (AA 25-609) (His tag)
Quick Overview for HSA Protein (AA 25-609) (His tag) (ABIN2181228)
Target
See all HSA ProteinsProtein Type
Origin
Source
Purity
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Protein Characteristics
- AA 25-609
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Purification tag / Conjugate
- This HSA protein is labelled with His tag.
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Sequence
- AA 25-609
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Characteristics
- This protein carries a polyhistidine tag at the C-terminus. The protein has a calculated MW of 67.3 kDa. The protein migrates as 66 kDa under reducing (R) condition (SDS-PAGE) due to glycosylation.
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Sterility
- 0.22 μm filtered
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Endotoxin Level
- Less than 1.0 EU per μg by the LAL method.
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Buffer
- PBS, pH 7.4
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Handling Advice
- Please avoid repeated freeze-thaw cycles.
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Storage
- -20 °C
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Storage Comment
- No activity loss was observed after storage at: In lyophilized state for 1 year (4 °C), After reconstitution under sterile conditions for 3 months (-70 °C).
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: "Peripheral Protein Unfolding Drives Membrane Bending." in: Langmuir : the ACS journal of surfaces and colloids, Vol. 34, Issue 28, pp. 8400-8407, (2019) (PubMed).
: "A quantitative Streptococcus pyogenes-human protein-protein interaction map reveals localization of opsonizing antibodies." in: Nature communications, Vol. 10, Issue 1, pp. 2727, (2019) (PubMed).
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: "Peripheral Protein Unfolding Drives Membrane Bending." in: Langmuir : the ACS journal of surfaces and colloids, Vol. 34, Issue 28, pp. 8400-8407, (2019) (PubMed).
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- HSA (Human Serum Albumin (HSA))
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Alternative Name
- HSA
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Background
- Serum albumin (SA) is also known as ALB, which is the main protein of plasma and has a good binding capacity for water,Ca2+,Na+,K+,fatty acids,hormones, bilirubin and drugs.The main function of SA is the regulation of the colloidal osmotic pressure of blood. As Major zinc transporter in plasma, SA typically binds about 80 % of all plasma zinc. A variant structure of albumin could lead to increased binding of zinc resulting in an asymptomatic augmentation of zinc concentration in the blood. Defects in serum albumin can cause familial dysalbuminemic hyperthyroxinemia which is a form of euthyroid hyperthyroxinemia that is due to increased affinity of serum albumin for T4. It is the most common cause of inherited euthyroid hyperthyroxinemia in Caucasian population.
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Molecular Weight
- 67.4 kDa
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NCBI Accession
- NP_000468
Target
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