ACTG1 (GeneName), Actin, cytoplasmic 2 (ProteinName), ACTG_HUMAN.
Human ACTG1/ Actin, cytoplasmic 2 ELISA Kit
Natural and recombinant human Actin, cytoplasmic 2
Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids
Polymerization of globular actin (G-actin) leads to a structural filament (F-actin) in the form of a two-stranded helix. Each actin can bind to 4 others.
Actins are highly conserved proteins that are involved in various types of cell motility and are ubiquitously expressed in all eukaryotic cells.
MEEEIAALVI | DNGSGMCKAG | FAGDDAPRAV | FPSIVGRPRH | QGVMVGMGQK |
DSYVGDEAQS | KRGILTLKYP | IEHGIVTNWD | DMEKIWHHTF | YNELRVAPEE |
HPVLLTEAPL | NPKANREKMT | QIMFETFNTP | AMYVAIQAVL | SLYASGRTTG |
IVMDSGDGVT | HTVPIYEGYA | LPHAILRLDL | AGRDLTDYLM | KILTERGYSF |
TTTAEREIVR | DIKEKLCYVA | LDFEQEMATA | ASSSSLEKSY | ELPDGQVITI |
GNERFRCPEA | LFQPSFLGME | SCGIHETTFN | SIMKCDVDIR | KDLYANTVLS |
GGTTMYPGIA | DRMQKEITAL | APSTMKIKII | APPERKYSVW | IGGSILASLS |
TFQQMWISKQ | EYDESGPSIV | HRKCF
This product has not yet been referenced specifically in any publications.
"A mutation in the gamma actin 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26)."
"Mutations in the gamma-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26)."
"Novel ACTG1 mutation causing autosomal dominant non-syndromic hearing impairment in a Chinese family."
"A recurrent de novo mutation in ACTG1 causes isolated ocular coloboma."
"De novo mutations in the actin genes ACTB and ACTG1 cause Baraitser-Winter syndrome."
"In vivo and in vitro effects of two novel gamma-actin (ACTG1) mutations that cause DFNA20/26 hearing impairment."
"Audiometric and vestibular features in a second Dutch DFNA20/26 family with a novel mutation in ACTG1."
"Beta and gamma-cytoplasmic actins display distinct distribution and functional diversity."
"Effects of human deafness gamma-actin mutations (DFNA20/26) on actin function."
"A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment."
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