추천 제품
일반 설명
The gene HSA (human serum albumin) is mapped to human chromosome 4q13.3. The gene encodes a protein of 585 amino acids with a molecular weight of 66.4kDa. HSA is the most abundant protein in the plasma and has many metal-binding sites.
애플리케이션
HSA (human serum albumin) has been used for the development of automated dye-binding method for serum albumin determination using bromcresol purple. It has also been used to study effect of HSA on DNA transfection by lipoplexes.
생화학적/생리학적 작용
HSA (human serum albumin) mainly works as a carrier for various nutrients, metabolites and xenobiotics. It interacts with plasma zinc and regulates uptake of zinc in cells. HSA plays a crucial role in drug pharmacokinetics. It also controls oncotic pressure and volume of the blood. Mutations in the gene are linked with congenital analbuminemia and familial dysalbuminemic hyperthyroxinemia.
물리적 형태
Sterile filtered yellowish liquid.
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
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시험 성적서(COA)
Lot/Batch Number
이미 열람한 고객
Structure and ligand binding properties of human serum albumin.
Kragh-Hansen U
Danish Medical Bulletin, 37, 57-84 (1990)
Structural basis of non-steroidal anti-inflammatory drug diclofenac binding to human serum albumin.
Zhang Y
Chemical Biology & Drug Design, 86, 1178-1184 (2015)
New automated dye-binding method for serum albumin determination with bromcresol purple.
Pinnell AE and Northam BE
Clinical Chemistry, 24, 80-86 (1978)
A nucleotide insertion and frameshift cause analbuminemia in an Italian family.
Watkins S
Proceedings of the National Academy of Sciences of the USA, 91, 2275-2279 (1994)
An identical missense mutation in the albumin gene results in familial dysalbuminemic hyperthyroxinemia in 8 unrelated families.
Sunthornthepvarakul T
Biochemical and Biophysical Research Communications, 202, 781-787 (1994)
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