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SAB4200261

Sigma-Aldrich

Anti-FIP1L1 (N-terminal) antibody produced in rabbit

~1.0 mg/mL, affinity isolated antibody

Synonym(s):

Anti-hFip1, Anti-FIP1, Anti-RHE, Anti-pre-mRNA 3’end processing factor FIP1

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About This Item

UNSPSC Code:
12352203
NACRES:
NA.41

biological source

rabbit

conjugate

unconjugated

antibody form

affinity isolated antibody

antibody product type

primary antibodies

clone

polyclonal

form

buffered aqueous solution

mol wt

antigen ~70 kDa

species reactivity

human

concentration

~1.0 mg/mL

technique(s)

indirect immunofluorescence: 2.5-5 μg/mL using paraformaldehyde fixed NIH-3T3 cells
western blot: 1-2 μg/mL using lysates of NIH-3T3 cells

UniProt accession no.

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

Gene Information

General description

The factor interacting with poly(a) polymerase α (PAPOLA) and cleavage and polyadenylation specificity factor 1 (CPSF1) (FIP1L1) gene is located on human chromosome 4q12. The encoded protein is a subunit of CPSF complex. FIP1L1 is composed of an acidic N-terminus region, a proline-rich domain and a C-terminal region of alternating arginines and aspartates (RD domain).

Specificity

Anti-FIP1L1 (N-terminal) recognizes human FIP1L1.

Immunogen

synthetic peptide corresponding to a sequence at the N- terminal region of human FIP1L1, conjugated to KLH. The corresponding sequence is identical in mouse and rat.

Application

Anti-FIP1L1 (N-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) induces the action of U-rich sequence element mediated poly(A) polymerase (PAP). Alterations in the gene results in a FIP1L1- platelet-derived growth factor receptor A (PDGFRA) fusion gene, which have been observed in conditions such as 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.

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), 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.

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Storage Class

10 - Combustible liquids

flash_point_f

Not applicable

flash_point_c

Not applicable


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Yoshiyuki Yamada et al.
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
Isabelle Kaufmann et al.
The EMBO journal, 23(3), 616-626 (2004-01-30)
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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