Alpha-1-fetoprotein recombinant protein

Reference: PX-P6414-100
Product nameAlpha-1-fetoprotein recombinant protein
Origin speciesHomo sapiens (Human)
Expression systemEukaryotic expression
Molecular weight68.58 kDa
Protein delivered with Tag?C-Terminal His Tag
Purity estimated>90% by SDS-PAGE
BufferPBS pH 7.4, 1mM EDTA, 4% Trehalose, 1% Mannitol
Delivery conditionDry Ice
Delivery lead time in business days3-5 days if in stock; 3-5 weeks if production needed
Storage condition4°C for short term (1 week), -20°C or -80°C for long term (avoid freezing/thawing cycles; addition of 20-40% glycerol improves cryoprotection)
BrandProteoGenix
Host speciesMammalian cells
Fragment TypeMet1-Val609
Aliases /SynonymsAlpha-fetoprotein, Alpha-1-fetoprotein, Alpha-fetoglobulin, AFP, HPAFP
ReferencePX-P6414
NoteFor research use only.

Description of Alpha-1-fetoprotein recombinant protein

Introduction:

Alpha-fetoprotein (AFP) is a glycoprotein that is primarily produced by the liver and yolk sac during fetal development. It serves as a marker for various diseases, including liver cancer, and has been extensively studied for its structure, activity and application as a drug target and biomarker. In this article, we will explore the characteristics of AFP and its related proteins, including Alpha-1-fetoprotein (AFP-L3) and Alpha-fetoglobulin (AFG), as well as the use of Human AFP/Alpha-fetoprotein recombinant protein (HPAFP) in research and clinical settings.

Structure of AFP:

AFP is a single-chain polypeptide with a molecular weight of approximately 70 kDa. It is composed of 591 amino acids and contains three carbohydrate chains, which contribute to its glycoprotein nature. The protein is primarily synthesized in the fetal liver and is found in high levels in the fetal circulation. In adults, the production of AFP is significantly reduced, and it is mainly found in trace amounts in the serum.

Activity of AFP:

AFP has multiple functions during fetal development, including regulating the transport of fatty acids and other nutrients from the mother to the fetus. It also plays a role in the development of the immune system and the maturation of the gastrointestinal tract. In adults, AFP levels are significantly elevated in certain diseases, such as liver cancer, where it has been identified as a potential biomarker for early detection and monitoring of the disease.

Alpha-1-fetoprotein (AFP-L3):

AFP-L3 is a variant of AFP that has been found to be highly specific for liver cancer. It is a glycoform of AFP that contains a fucosylated sugar chain, making it distinct from the normal AFP found in healthy individuals. This variant has been shown to be present in high levels in patients with hepatocellular carcinoma (HCC) and has been proposed as a more sensitive biomarker for the disease compared to traditional AFP levels.

Alpha-fetoglobulin (AFG):
AFG is another protein that is closely related to AFP. It is also a glycoprotein and shares structural similarities with AFP, including the presence of three carbohydrate chains. AFG is found in high levels in fetal serum but is also present in small amounts in adult serum. It has been suggested that AFG may have a similar role to AFP in regulating the transport of nutrients from the mother to the fetus.

Application of AFP and related proteins:

The use of AFP and its related proteins as biomarkers for liver cancer has been extensively studied. Elevated levels of AFP have been associated with HCC, and it is routinely used as a diagnostic marker for the disease. However, the low specificity of AFP has led to the development of other biomarkers, such as AFP-L3 and AFG, which have shown promising results in detecting early-stage HCC.

In addition to its role as a biomarker, AFP and its variants have also been investigated as potential drug targets. Researchers have identified specific receptors on the surface of cancer cells that bind to AFP, and this interaction has been targeted for potential therapeutic interventions. Furthermore, HPAFP, a recombinant form of AFP, has been used in research studies to understand the role of AFP in cancer development and to develop new treatment strategies.

Conclusion:

In summary, AFP and its related proteins, including AFP-L3 and AFG, have been extensively studied for their structure, activity, and potential applications as biomarkers and drug targets. The use of these proteins in research and clinical settings has provided valuable insights into the role of AFP in fetal development and its potential as a diagnostic and therapeutic tool in liver cancer. Further research in this area may lead to the development of more effective treatments for HCC and other diseases associated with AFP.

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