Anti-Human PRDM3 Polyclonal Antibody

The protein encoded by this gene is a transcriptional regulator and oncoprotein that may be involved in hematopoiesis, apoptosis, development, and cell differentiation and proliferation. The encoded protein can interact with CTBP1, SMAD3, CREBBP, KAT2B, MAPK8, and MAPK9. This gene can undergo translocation with the AML1 gene, resulting in overexpression of this gene and the onset of leukemia. Several transcript variants encoding a few different isoforms have been found for this gene.MECOM (MDS1 And EVI1 Complex Locus) is a Protein Coding gene. Diseases associated with MECOM include Radioulnar Synostosis With Amegakaryocytic Thrombocytopenia 2 and Acute Myeloid Leukemia With Inv3(P21;Q26.2) Or T(3;3)(P21;Q26.2). Among its related pathways are MAPK signaling pathway and Pathways in cancer. GO annotations related to this gene include nucleic acid binding and protein homodimerization activity. An important paralog of this gene is PRDM16.
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Properties

Data Sheet Click for Datasheet
Catalog Number PA05625
Size 100μl
Host Type Rabbit
Immunogen Synthesized peptide derived from the N-terminal region of human PRDM3
Specificity
Isotype IgG
Reacitivity Human
Clone
Uniprot Q13465
Concentration 1mg/mL
Dilution WB 1:500-1:2000, IHC 1:100-1:300, ELISA 1:20000
Formulation
Application WB,IHC-p,ELISA
Other Names MDS1,MDS1 EVI1,MDS1EVI1,Myelodysplasia syndrome 1,Myelodysplasia syndrome associated protein 1,PRDM 3,PRDM3
Storage Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript For research use only, not for use in diagnostic procedures.

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