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Anti-Pbx1a monoclonal antibody


Stanford Reference:

01-245A


Abstract


Researchers in the laboratory of Dr. Michael Cleary at Stanford University have developed anti-Pbx1a monoclonal antibodies to study transcriptional regulation, embryonic development, and tissue homeostasis. Mammalian Pbx genes encode a family of TALE (three amino acid loop extension) homeodomain proteins that function as transcriptional regulators in numerous cell types.

Pbx1 was originally identified in human pre-B acute lymphoblastic leukemias. Lack of Pbx1 results in embryonic lethality and is associated with multiple patterning malformations, hypoplasia or aplasia of most internal organs, organ malfunctions, and severe fetal anemia. Pbx1 is the prototypic Pbx family member and encodes the alternatively spliced Pbx1a and Pbx1b isoforms that exhibit characteristic biochemical properties. Pbx1a is the high molecular-weight protein form. Pbx1 utilizes the alternative portions of itself to interact with Meis versus Hox proteins. The anti-Pbx1a antibodies could be used in studies of leukemia, embryonic development, and tissue homeostasis.


Applications


  • Research related to:
    • leukemia
    • embryonic development
    • tissue homeostasis

Publications



Web Site


Cleary Lab

Innovators & Portfolio



Date Released

 4/21/2015
 

Licensing Contact


Brenda Martino, Biological Materials Specialist
(650) 725-9119 (Direct)
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Related Keywords


leukemia   transcription factors   research tool   research tool: antibody   research tool: cell line   
 

   

  

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78-017 Monoclonal Antibodies: 11-6 anti-Ig-5b, 11-5 anti-I-A (2), 11-4 anti-H-2Kk, 11-3 anti-I-A917), 10-4 anti-Ig-5a, H-12 anti-THY 1.2
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S01-245A Anti-Pbx1a monoclonal antibody