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RP1 抗体

(Retinitis Pigmentosa 1 (Autosomal Dominant) (RP1))
This gene encodes a member of the doublecortin family. The protein encoded by this gene contains two doublecortin domains, which bind microtubules and regulate microtubule polymerization. The encoded protein is a photoreceptor microtubule-associated protein and is required for correct stacking of outer segment disc. This protein and the RP1L1 protein, another retinal-specific protein, play essential and synergistic roles in affecting photosensitivity and outer segment morphogenesis of rod photoreceptors. Because of its response to in vivo retinal oxygen levels, this protein was initially named ORP1 (oxygen-regulated protein-1). This protein was subsequently designated RP1 (retinitis pigmentosa 1) when it was found that mutations in this gene cause autosomal dominant retinitis pigmentosa. Mutations in this gene also cause autosomal recessive retinitis pigmentosa. Two transcript variants encoding distinct isoforms are resulted from alternative promoters and alternative splicing. [provided by RefSeq, Sep 2010].

Popular RP1 抗体

Aliases for RP1 抗体

RP1, axonemal microtubule associated L homeolog (rp1.L) 抗体
RP1, axonemal microtubule associated (RP1) 抗体
retinitis pigmentosa 1 (autosomal dominant) (rp1) 抗体
uncharacterized LOC100355685 (LOC100355685) 抗体
RP1, axonemal microtubule associated (Rp1) 抗体
retinitis pigmentosa 1 (human) (Rp1) 抗体
Dcdc3 抗体
DCDC4A 抗体
mG145 抗体
MGC83581 抗体
orp1 抗体
ORP1 抗体
Orp1 抗体
Rp1h 抗体
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