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Myosin VIIA Produkte

(Myosin VIIA (MYO7A))

Kategorien

This gene is a member of the myosin gene family. Myosins are mechanochemical proteins characterized by the presence of a motor domain, an actin-binding domain, a neck domain that interacts with other proteins, and a tail domain that serves as an anchor. This gene encodes an unconventional myosin with a very short tail. Defects in this gene are associated with the mouse shaker-1 phenotype and the human Usher syndrome 1B which are characterized by deafness, reduced vestibular function, and (in human) retinal degeneration. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008].

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Ausgewählte Myosin VIIA Kategorien

Myosin VIIA Antikörper

High quality antibodies with extensive validation data.

Empfohlene Myosin VIIA Antikörper

Produkt
Reaktivität
Applikation
Validierungen
Kat. Nr.
Menge
Datenblatt
Reaktivität Human, Mouse
Applikation ELISA, IHC
Validierungen
  • (2)
  • (1)
Kat. Nr. ABIN2435036
Menge 200 μL
Datenblatt Datenblatt
Reaktivität Human
Applikation ELISA, IHC, IF
Validierungen
  • (3)
Kat. Nr. ABIN7174961
Menge 100 μg
Datenblatt Datenblatt
Reaktivität Human, Mouse
Applikation ELISA, IF (cc), IF (p), IHC (fro), IHC (p)
Validierungen
  • (2)
Kat. Nr. ABIN872519
Menge 100 μL
Datenblatt Datenblatt

Empfohlene Myosin VIIA Proteine

Produkt
Reaktivität
Source
Validierungen
Kat. Nr.
Menge
Datenblatt
Reaktivität Human
Source Wheat germ
Validierungen
  • (1)
Kat. Nr. ABIN1311832
Menge 10 μg
Datenblatt Datenblatt
Reaktivität Human
Source Escherichia coli (E. coli)
Validierungen
Kat. Nr. ABIN7422445
Menge 100 μg
Datenblatt Datenblatt

Neueste Publikationen zu unseren Myosin VIIA Produkten

Schulze, Sasse, Prenzler, Staecker, Mellott, Roemer, Durisin, Lenarz, Warnecke: "Microenvironmental support for cell delivery to the inner ear." in: Hearing research, Vol. 368, pp. 109-122, (2018) (PubMed).

Mellott, Shinogle, Nelson-Brantley, Detamore, Staecker: "Exploiting decellularized cochleae as scaffolds for inner ear tissue engineering." in: Stem cell research & therapy, Vol. 8, Issue 1, pp. 41, (2017) (PubMed).

Mellott, Devarajan, Shinogle, Moore, Talata, Laurence, Forrest, Noji, Tanaka, Staecker, Detamore: "Nonviral Reprogramming of Human Wharton's Jelly Cells Reveals Differences Between ATOH1 Homologues." in: Tissue engineering. Part A, Vol. 21, Issue 11-12, pp. 1795-809, (2015) (PubMed).

Jeon, Fujioka, Kim, Edge: "Notch signaling alters sensory or neuronal cell fate specification of inner ear stem cells." in: The Journal of neuroscience : the official journal of the Society for Neuroscience, Vol. 31, Issue 23, pp. 8351-8, (2011) (PubMed).

Smeti, Savary, Capelle, Hugnot, Uziel, Zine: "Expression of candidate markers for stem/progenitor cells in the inner ears of developing and adult GFAP and nestin promoter-GFP transgenic mice." in: Gene expression patterns : GEP, Vol. 11, Issue 1-2, pp. 22-32, (2011) (PubMed).

Weston, Pierce, Jensen-Smith, Fritzsch, Rocha-Sanchez, Beisel, Soukup: "MicroRNA-183 family expression in hair cell development and requirement of microRNAs for hair cell maintenance and survival." in: Developmental dynamics : an official publication of the American Association of Anatomists, Vol. 240, Issue 4, pp. 808-19, (2011) (PubMed).

Dong, Sui, Yamaguchi, Kamitori, Hirata, Suzuki, Holley, Tokuda: "Role of phosphatase and tensin homolog in the development of the mammalian auditory system." in: Neuroreport, Vol. 21, Issue 10, pp. 731-5, (2010) (PubMed).

Xia, Gao, Yuan, Osborn, Bress, Pfister, Maricich, Pereira, Oghalai: "Deficient forward transduction and enhanced reverse transduction in the alpha tectorin C1509G human hearing loss mutation." in: Disease models & mechanisms, Vol. 3, Issue 3-4, pp. 209-23, (2010) (PubMed).

Tan, Lee, Ruan: "Bone-marrow-derived cells that home to acoustic deafened cochlea preserved their hematopoietic identity." in: The Journal of comparative neurology, Vol. 509, Issue 2, pp. 167-79, (2008) (PubMed).

Longo-Guess, Gagnon, Cook, Wu, Zheng, Johnson: "A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry (hscy) mice." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 102, Issue 22, pp. 7894-9, (2005) (PubMed).

Synonyme und alternative Namen zu Myosin VIIA

crinkled (ck), myosin VIIAa (myo7aa), myosin VIIa (LOAG_02192), myosin VIIA (MYO7A), myosin VIIA (myo7a), myosin 7A (LOC663995), myosin-VIIa (LOC100116446), myosin VIIA (Myo7a), 53D10S, anon-35Bb, BG:DS00929.11, br27, CG7595, ck/MyoVIIA, D, D2, DFNA11, DFNB2, DM7a, Dm 35B, Dmel\\CG7595, DmVIIA, DmVIIa, DMyoVIIa, Dro35B, ESTS:53D10S, Hdb, l(1)35Ca, l(2)07130, l(2)35Ca, l(2)br27, l35Ca, Mhc35BC, Myo7, myo7a, MYO7A, MyoVIIA, myoVIIA, MYOVIIA, MYU7A, nmf371, NSRD2, NV17859, polka, sh-1, sh1, stc, stch, USH1B

Bezeichner auf Proteinebene für Myosin VIIA

  • CG7595-PA
  • CG7595-PB
  • ck-PA
  • ck-PB
  • lethal 27 in the black-reduced region
  • lethal group D2
  • myosin 7a
  • myosin 7a heavy chain
  • myosin VII
  • myosin VIIa
  • myosin heavy chain at 35BC
  • myosin-VII
  • mysoin VIIa
  • stubby chaetae
  • transcription unit D
  • mar
  • mariner
  • myosin-VIIa
  • myosin VIIA
  • myosin-VIIa-like
  • myosin 7A
  • GLEAN_13346
  • motor protein
  • shaker 1
  • unconventional myosin-VIIa
  • myosin VIIA (Usher syndrome 1B (autosomal recessive, severe))
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