Monoclonal Antibody Against Human Blood Group Lea (4620)
Cat. No:
FNK-2AHBGLA
Clone No:
Hyb-4620
Manufacturing Process:
Hybridoma obtained by fusing mouse myeloma cells (NS-1) with BALB/c mouse spleen cells immunized with blood group substance derived from human saliva is proliferated in the BALB/c mouse abdominal cavity and ascites is collected.
Specificity:
This monoclonal antibody specifically agglutinates human blood group Le(a+b-) red blood cells (coombs test).
Purification:
Ammonium sulfate precipitation.
Ig Class:
IgG1
Form:
Saline (containing 0.1% NaN3)
Protein Concentration:
0.5 mg/mL
Package:
0.2 mL
Storage:
2-8℃ (Below -20℃ for long term storage)
Shipping Condition:
Dry Ice
Application:
Hemagglutination
Antigen Characterization
Type: Primary
Application: ELISA, Western Blot
Species: Human
Recombinant: Yes
Human Diseases
Bombay Phenotype (hh): Individuals with this phenotype lack the H antigen, which is necessary for the formation of Lewis antigens, leading to potential complications in blood transfusions and organ transplants.
Gastrointestinal Infections: Lewis antigens, including Lea, have been associated with susceptibility to infections such as Helicobacter pylori, which can lead to gastric diseases.
Transfusion Reactions: Mismatched blood transfusions involving Lewis antigens can lead to adverse reactions, particularly in individuals with anti-Lea antibodies.
Cancer: Altered expression of Lewis antigens has been linked to tumor progression and metastasis in various cancers, where they may influence immune evasion and cell adhesion.
Cellular Signaling Pathways
Cell Adhesion and Migration: The Lea antigen is involved in cell-cell interactions and adhesion processes, influencing leukocyte migration during inflammatory responses.
Immune Response Modulation: The presence of Lea can affect T cell activation and differentiation, thereby modulating overall immune responses.
Interaction with Pathogens: Lewis antigens may serve as receptors for certain pathogens, influencing their ability to adhere to host tissues and evade immune detection.
Glycosylation Pathways: The synthesis of Lea involves specific glycosyltransferases that add fucose residues to oligosaccharides, impacting various cellular functions related to glycosylation.
Aliases for Lea (Lewis a) Gene
Lewis A antigen (Lea)
Le(a) antigen
Lewis blood group antigen A
Le(a) glycoprotein
References
WF;, Dunstan RA;Simpson MB;Rosse. “Lea Blood Group Antigen on Human Platelets.” American Journal of Clinical Pathology, U.S. National Library of Medicine, pubmed.ncbi.nlm.nih.gov/3966446/.
Subramaniyan, Rajeswari. “Serological Characteristics of Lewis Antibodies and Their Clinical Significance - a Case Series.” Hematology, Transfusion and Cell Therapy, U.S. National Library of Medicine, 2023, www.ncbi.nlm.nih.gov/pmc/articles/PMC10244237/.
"Lewis System: Anti-Lewis.” Professional Education, 30 Jan. 2023, professionaleducation.blood.ca/en/transfusion/best-practices/serological-best-practices/lewis-system-anti-lewis.
“The Lewis Blood Group System and Secretor Status.” Biomedical Scientist, 23 Jan. 2024, thebiomedicalscientist.net/2019/01/07/lewis-blood-group-system-and-secretor-status.
Dean L. Blood Groups and Red Cell Antigens [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 2005. Chapter 6, The Hh blood group. Available from: https://www.ncbi.nlm.nih.gov/books/NBK2268/
Alhajj M, Zubair M, Farhana A. Enzyme Linked Immunosorbent Assay. [Updated 2023 Apr 23]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan-. Available from: https://www.ncbi.nlm.nih.gov/books/NBK555922/
Ewald, D. R., & Sumner, S. C. (2016). Blood type biochemistry and human disease. Wiley interdisciplinary reviews. Systems biology and medicine, 8(6), 517–535. https://doi.org/10.1002/wsbm.1355