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ARHGEF9 rabbit pAb - 100 μL

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The protein encoded by this gene is a Rho-like GTPase that switches between the active (GTP-bound) state and inactive (GDP-bound) state to regulate CDC42 and other genes. Defects in this gene are a cause of startle disease with epilepsy (STHEE), also known as hyperekplexia with epilepsy. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2010],

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Expédition : 2-3 jours ouvrables

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ARHGEF9 rabbit pAb
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