Aaas (GeneName), Aladin (ProteinName), AAAS_MOUSE.
Mouse Aaas/ Aladin ELISA Kit
Natural and recombinant mouse Aladin
Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids
Interacts with NDC1, the interaction is required for nuclear pore localization.
Plays a role in the normal development of the peripheral and central nervous system.
Nucleus Nuclear pore complex
MCSLGLFPPP | PPRGQVTLYE | HNNELVTGNS | YESPPPDFRG | QWINLPVLHL |
TKDPLKAPGR | LDHGTRTAFI | HHREQVWKRC | INVWHDVGLF | GVLNEIANSE |
EEVFEWVKTA | CSWALALCGR | ASSLHGSLFP | HLSLRSEDLI | AEFAQVTNWS |
SCCLRVFAWH | PHTNKFAVAL | LDDSIRVYNA | NSTIVPSLKH | RLQRNVAALA |
WKPLSASVLA | VACQSCILIW | TLDPTSLSTR | PSSGCAQVLS | HPGHTPVTSL |
AWAPNGGWLL | SASPVDAVIL | VWDVSTETCV | PLPWFRGGGV | TNLLWSPDGS |
KVLATTPSAV | FRVWEAQMWT | CEAWPTLSGR | CQTGCWSPDG | NRLLFTVLGE |
ALIYSLSFPE | RCGTGKGHVG | GAKSATIVAD | LSETTIQTPD | GEERLGGEAH |
SMVWDPSGER | LAVLMKGNPQ | VQDGNPVILL | FRTRNSPVFE | LLPCGIIQGE |
PGAQAQLITF | HPSFNKGALL | SVCWSTGRIT | HIPLYFVNAQ | FPRFSPVLGR |
AQEPPAGGGG | SIHEVPLFTE | TSPTSAPWDP | LPGQSSAQPH | SPHSHL
This product has not yet been referenced specifically in any publications.
"Mutant WD-repeat protein in triple-A syndrome."
"The nuclear pore complex protein ALADIN is anchored via NDC1 but not via POM121 and GP210 in the nuclear envelope."
"Molecular cloning and characterization of AAAS-V2, a novel splice variant of human AAAS."
"Proteomic analysis of the mammalian nuclear pore complex."
"Triple A syndrome is caused by mutations in AAAS, a new WD-repeat protein gene."
"Triple A or Allgrove syndrome. A case report with ophthalmic abnormalities and a novel mutation in the AAAS gene."
"Tissue-specific expression and subcellular localization of ALADIN, the absence of which causes human triple A syndrome."
"The transmembrane nucleoporin NDC1 is required for targeting of ALADIN to nuclear pore complexes."
"Deficiency of ferritin heavy-chain nuclear import in triple a syndrome implies nuclear oxidative damage as the primary disease mechanism."
"A novel AAAS gene mutation (p.R194X) in a patient with triple A syndrome."
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