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Unconventional myosin-Ih Antibodies

AND Myo1h ELISA kits, Unconventional myosin-Ih Proteins

Many biological assays use antibodies to detect Unconventional myosin-Ih, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with Unconventional myosin-Ih in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop Unconventional myosin-Ih antibodies...

We validate the specificity of these antibodies to Unconventional myosin-Ih by testing them on tissues known to express Myo1h positively and negatively. Browse below to find the Myo1h antibody that suites your experiment. We have 0 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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Myo1h Infographic by Boster Bio

Myo1h protein infographic

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Myo1h Overview

Facts about Unconventional myosin-Ih.

Unconventional myosin-Ih (Myo1h)

Myosins are actin-based motor molecules with ATPase activity. Unconventional myosins serve in intracellular movements.

Their highly divergent tails are presumed to bind to membranous compartments, which would be moved relative to actin filaments (By similarity). .

Gene Information

Mouse
Gene Name:	Myo1h
Uniprot:	Q9D6A1
Entrez:	231646

Gene Information

Family

Belongs to:

TRAFAC class myosin-kinesin ATPase superfamily

Family

Alternative Names

myosin IH; myosin-1H; myosin-Ih

Molecular Weight

Mass (kDA):
109.993 kDA

Molecular Weight

Genomic Context


Mouse

Location:	5\|5 F
Sequence:	5;

Tissue Specificity

Expressed in neonatal inner-ear organs.

Diseases

Spastic Paraplegia 36, Autosomal Dominant
Spastic Paraplegia, Hereditary
Mandibular Prognathism
Overjet
Malocclusion
Peripheral Motor Neuropathy
Peroneal Muscular Atrophy With Pyramidal Features, Autosomal Dominant
Prognathism
Paraplegia

Peripheral Neuropathy
Spastic Paraplegia
Spastic Paraplegia 10, Autosomal Dominant

Disease

Pathways

Transport
Vesicle Transport
Phagocytosis
Cell Motility
Localization

Pathways

PTMs

Phosphoprotein

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For details, visit:
bosterbio.com/bosterbio-gene-info-cards/Myo1h

References

PMID: 12486594 by Dumont R.A., et al. Myosin-I isozymes in neonatal rodent auditory and vestibular epithelia.