RBM10 抗体
(RNA Binding Motif Protein 10 (RBM10))
This gene encodes a nuclear protein that belongs to a family proteins that contain an RNA-binding motif. The encoded protein associates with hnRNP proteins and may be involved in regulating alternative splicing. Defects in this gene are the cause of the X-linked recessive disorder, TARP syndrome. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Mar 2011].
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Latest Publications for our RBM10 抗体
: "The nuclear splicing factor RNA binding motif 5 promotes caspase activation in human neuronal cells, and increases after traumatic brain injury in mice." in: Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism, Vol. 35, Issue 4, pp. 655-66, (2015) (PubMed).: "A quantitative atlas of mitotic phosphorylation." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 105, Issue 31, pp. 10762-7, (2008) (PubMed).
Aliases for RBM10 抗体
RNA binding motif protein 10 (RBM10) 抗体RNA binding motif protein 10 (rbm10) 抗体
RNA binding motif protein 10 (Rbm10) 抗体
DXS8237E 抗体
E430039K10Rik 抗体
GPATC9 抗体
GPATCH9 抗体
RBM10 抗体
S1-1 抗体
TARPS 抗体
ZRANB5 抗体
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