The factor interacting with poly(a) polymerase α (PAPOLA) and cleavage and polyadenylation specificity factor 1 (CPSF1) (FIP1L1) is a subunit of CPSF complex. FIP1L1 contains an acidic N-terminal region, a proline-rich domain and a C-terminal region of alternating arginines and aspartates (RD domain). The FIP1L1 gene is mapped to human chromosome 4q12.
Specificity
Anti-FIP1L1 (C-terminal) recognizes human FIP1L1.
Immunogen
synthetic peptide corresponding to a sequence at the C- terminal region of human FIP1L1 conjugated to KLH. The corresponding sequence is identical in mouse and rat.
Application
Anti-FIP1L1 (C-terminal) antibody produced in rabbit is suitable for immunoblotting and immunofluorescence.
Biochem/physiol Actions
The factor interacting with poly(a) polymerase α (PAPOLA) and cleavage and polyadenylation specificity factor 1 (CPSF1) (FIP1L1) is known to promote the U-rich sequence element mediated poly(A) polymerase (PAP) action. Genetic rearrangements that result in a FIP1L1- platelet-derived growth factor receptor A (PDGFRA) fusion gene have been identified in patients with hypereosinophilic syndrome/chronic eosinophilic leukemia (CEL) and in systemic mast cell disease.
Physical form
Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.
Storage and Stability
For continuous use, store at 2-8 °C for up toone month. For extended storage, freeze in working aliquots. Repeated freezing and thawing, or storage in “frost-free” freezers, is not recommended. If slight turbidity occurs upon prolonged storage, clarify the solution by centrifugation before use. Working dilutions should be discarded if not used within 12 hours.
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Unless otherwise stated in our catalog, our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
International archives of allergy and immunology, 152 Suppl 1, 101-105 (2010-06-11)
Since the identification of the FIP1L1/PDGFRA fusion gene as a pathogenic cause of the hypereosinophilic syndrome (HES), the importance of the molecular classification of HES leading to the diagnosis of chronic eosinophilic leukemia (CEL) has been recognized. As a result
In mammals, polyadenylation of mRNA precursors (pre-mRNAs) by poly(A) polymerase (PAP) depends on cleavage and polyadenylation specificity factor (CPSF). CPSF is a multisubunit complex that binds to the canonical AAUAAA hexamer and to U-rich upstream sequence elements on the pre-mRNA
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