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Browse our Myosin VIIA (MYO7A) ELISA Kits

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Myosin VIIA ELISA Kits (MYO7A)
On are 0 Myosin VIIA (MYO7A) ELISA Kits from different suppliers available. Additionally we are shipping Myosin VIIA Antibodies (40) and and many more products for this protein. A total of 43 Myosin VIIA products are currently listed.
53D10S, anon-35Bb, BG:DS00929.11, br27, CG7595, ck/MyoVIIA, D, D2, DFNA11, DFNB2, DM7a, Dm 35B, Dmel\\CG7595, DmVIIa, DMyoVIIa, Dro35B, ESTS:53D10S, Hdb, l(1)35Ca, l(2)07130, l(2)35Ca, l(2)br27, l35Ca, Mhc35BC, Myo7, MYO7A, MYOVIIA, MYU7A, nmf371, NSRD2, NV17859, polka, sh-1, sh1, stc, stch, USH1B
list all ELISA KIts Gene Name GeneID UniProt
Mouse MYO7A MYO7A 17921 P97479
Human MYO7A MYO7A 4647 Q13402
Rat MYO7A MYO7A 266714  

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More ELISA Kits for Myosin VIIA Interaction Partners

Fruit Fly (Drosophila melanogaster) Myosin VIIA (MYO7A) interaction partners

  1. CK selectively interacts with the initia (show CASP8 ELISA Kits)tor caspase DRONC and regulates some of its non-a (show RIPK1 ELISA Kits)poptotic f (show CASP8 ELISA Kits)unctions. Results expose a conserved role for unconventional myosins in transducing caspase-d (show CASP3 ELISA Kits)ependent regulation of kinases.

  2. Data suggest that Crinkled acts in concert with Wingless targets to orchestrate the proper shaping of denticles in the Drosophila embryonic epidermis.

  3. Product identified as myosin VIIA.

  4. Loss of ck/myoVIIA function leads to complete deafness in Drosophila by disrupting the integrity of the scolopidia that transduce auditory signals.

  5. myosin VIIA is classified to be a high duty ratio motor

  6. kinetic behavior would allow myosin VIIa to exert and hold tension on actin filaments and, if dimerized, to function as a processive cargo transporter.

  7. domain markedly inhibits the actin (show ACTB ELISA Kits)-activated ATPase (show DNAH8 ELISA Kits) activity of tailless (show NR2E1 ELISA Kits) DM7A at low Ca(2 (show CA2 ELISA Kits)+) but not high Ca(2 (show CA2 ELISA Kits)+)

Zebrafish Myosin VIIA (MYO7A) interaction partners

  1. Study identified a new hair cell-specific enhancer located within Intron 2-3 of zebrafish myo7aa gene and highly conserved between species

  2. Zebrafish cone photoreceptors possess a large and well-differentiated accessory outer segment, in which the unconventional motor protein Myo7a is highly enriched.

  3. Data show that myo7a is localized in actin-rich ellipsoids of fish cones.

Mouse (Murine) Myosin VIIA (MYO7A) interaction partners

  1. MYO7A binds to and impinges on CASPASE-8 (show CASP8 ELISA Kits), revealing a new regulatory axis affecting RIPK1 (show RIPK1 ELISA Kits)>CASPASE-8 (show CASP8 ELISA Kits) signaling. Results expose a conserved role for unconventional myosins in transducing caspase (show CASP3 ELISA Kits)-dependent regulation of kinases.

  2. Myo7a interacts with integrin beta5 and selectively promotes integrin alphavbeta5-mediated cell migration

  3. Data show that myosin7a (Myo7a; sh1) deficiency causes severe retinal dysfunctions in albino sh1-/- mice.

  4. The family was found to segregate novel mutations of two different genes: myosin VIIA (MYO7A), and phosphodiesterase 6B, which causes nonsyndromic retinitis pigmentosa.

  5. the importance of MYO7A for the development and maintenance of bundle function

  6. the results support a role for MYO7A in the translocation of RPE65 (show RPE65 ELISA Kits), illustrating the involvement of a molecular motor (show MYO1B ELISA Kits) in the spatiotemporal organization of the retinoid cycle in vision.

  7. the myosin VIIa is a "slow", monomeric molecular motor (show MYO1B ELISA Kits) with a duty ratio of 0.6.

  8. we examine the effects of null mutation of the Ush1c (show USH1C ELISA Kits) gene on subcellular localization of Myo7a, Pcdh15 (show PCDH15 ELISA Kits) and Sans in the inner ear.

  9. crystal structure of MYO7A MyTH4-FERM domains in complex with the central domain (CEN) of Sans at 2.8 angstrom resolution; MyTH4-FERM/CEN complex structure provides mechanistic explanations for known deafness-causing mutations in MYO7A MyTH4-FERM

  10. Cadherin-23 (show CDH23 ELISA Kits), myosin VIIa and harmonin (show USH1C ELISA Kits) form a ternary complex and interact with phospholipids.

Human Myosin VIIA (MYO7A) interaction partners

  1. An unreported splice site mutation c.3924+1G > C compound with c.6028G > A in the MYO7A gene were detected to cosegregate with Usher syndrome type 2 in a Han Chinese family.

  2. There are more than 39 deafness genes reported to cause non-syndromic hereditary hearing loss (HHL) in Iran, of which the most prevalent causative genes include GJB2, SLC26A4, MYO15A, and MYO7A. In addition, we highlight some of the more common genetic causes of syndromic HHL in Iran. [review]

  3. This study showed that Mendelian sensorineural hearing loss exhibits vestibular dysfunction, including DFNA9 (show COCH ELISA Kits), DFNA11, DFNA15 (show POU4F3 ELISA Kits) and DFNA28 (show GRHL2 ELISA Kits).

  4. The novel compound heterozygous mutations (c.3671C>A and c.390_391insC) in MYO7A gene identified in this study were responsible for the autosomal recessive sensorineural hearing loss of this Chinese family

  5. MYO7A binds to and impinges on CASPASE-8 (show CASP8 ELISA Kits), revealing a new regulatory axis affecting RIPK1 (show RIPK1 ELISA Kits)>CASPASE-8 (show CASP8 ELISA Kits) signaling. Results expose a conserved role for unconventional myosins in transducing caspase (show CASP3 ELISA Kits)-dependent regulation of kinases.

  6. The genetic correction of MYO7A mutation resulted in morphologic and functional recovery of hair cell-like cells derived from induced pluripotent stem cells from a deaf patient.

  7. Ten variants in the MYO7A gene and 34 variants in the USH2A (show USH2A ELISA Kits) gene were detected in Italian patients with Usher syndrome at a high detection rate.

  8. concluded that the USH1 in this family was caused by compound heterozygous mutations in MYO7A

  9. Electron microscopy revealed that myosin VIIA is a monomer in which the tail domain bends back toward the head-neck domain to form a compact structure. This compact structure is extended at high ionic strength or in the presence of Ca(2 (show CA2 ELISA Kits)+).

  10. Clinical phenotypes of Usher syndrome associated with MYO7A mutations.

Myosin VIIA (MYO7A) Antigen Profile

Antigen Summary

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.

Alternative names and synonyms associated with Myosin VIIA (MYO7A)

  • crinkled (ck) Elisa Kit
  • myosin VIIAa (myo7aa) Elisa Kit
  • myosin VIIa (LOAG_02192) Elisa Kit
  • myosin VIIA (MYO7A) Elisa Kit
  • myosin VIIA (myo7a) Elisa Kit
  • myosin 7A (Myo7A) Elisa Kit
  • myosin VIIA (Myo7a) Elisa Kit
  • 53D10S Elisa Kit
  • anon-35Bb Elisa Kit
  • BG:DS00929.11 Elisa Kit
  • br27 Elisa Kit
  • CG7595 Elisa Kit
  • ck/MyoVIIA Elisa Kit
  • D Elisa Kit
  • D2 Elisa Kit
  • DFNA11 Elisa Kit
  • DFNB2 Elisa Kit
  • DM7a Elisa Kit
  • Dm 35B Elisa Kit
  • Dmel\\CG7595 Elisa Kit
  • DmVIIa Elisa Kit
  • DMyoVIIa Elisa Kit
  • Dro35B Elisa Kit
  • ESTS:53D10S Elisa Kit
  • Hdb Elisa Kit
  • l(1)35Ca Elisa Kit
  • l(2)07130 Elisa Kit
  • l(2)35Ca Elisa Kit
  • l(2)br27 Elisa Kit
  • l35Ca Elisa Kit
  • Mhc35BC Elisa Kit
  • Myo7 Elisa Kit
  • MYO7A Elisa Kit
  • MYOVIIA Elisa Kit
  • MYU7A Elisa Kit
  • nmf371 Elisa Kit
  • NSRD2 Elisa Kit
  • NV17859 Elisa Kit
  • polka Elisa Kit
  • sh-1 Elisa Kit
  • sh1 Elisa Kit
  • stc Elisa Kit
  • stch Elisa Kit
  • USH1B Elisa Kit

Protein level used designations for Myosin VIIA (MYO7A) ELISA Kits

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))

34882 Drosophila melanogaster
252846 Danio rerio
9939576 Loa loa
100478193 Ailuropoda melanoleuca
100543555 Meleagris gallopavo
100551824 Anolis carolinensis
466717 Pan troglodytes
663995 Tribolium castaneum
699411 Macaca mulatta
100116446 Nasonia vitripennis
17921 Mus musculus
4647 Homo sapiens
266714 Rattus norvegicus
397373 Sus scrofa
419085 Gallus gallus
485174 Canis lupus familiaris
535092 Bos taurus
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