WIPF1 抗体
(WAS/WASL Interacting Protein Family, Member 1 (WIPF1))
This gene encodes a protein that plays an important role in the organization of the actin cytoskeleton. The encoded protein binds to a region of Wiskott-Aldrich syndrome protein that is frequently mutated in Wiskott-Aldrich syndrome, an X-linked recessive disorder. Impairment of the interaction between these two proteins may contribute to the disease. Two transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jul 2008].
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Latest Publications for our WIPF1 抗体
: "WIP/WASp-based actin-polymerization machinery is essential for myoblast fusion in Drosophila." in: Developmental cell, Vol. 12, Issue 4, pp. 557-69, (2007) (PubMed).
: "The verprolin family of proteins: regulators of cell morphogenesis and endocytosis." in: FEBS letters, Vol. 579, Issue 24, pp. 5253-9, (2005) (PubMed).
: "The verprolin family of proteins: regulators of cell morphogenesis and endocytosis." in: FEBS letters, Vol. 579, Issue 24, pp. 5253-9, (2005) (PubMed).
Aliases for WIPF1 抗体
WAS/WASL interacting protein family member 1 (WIPF1) 抗体WAS/WASL interacting protein family, member 1 (Wipf1) 抗体
AI115543 抗体
D2Ertd120e 抗体
PRPL-2 抗体
WASPIP 抗体
Waspip 抗体
WIP 抗体
Wip 抗体
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