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TMIE antibody (Middle Region)
TMIE
Reactivity: Human
WB, EIA
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-TMIE Antibody
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Target
See all TMIE Antibodies
TMIE
(Transmembrane Inner Ear (TMIE))
Binding Specificity
All epitopes for TMIE antibodies
AA 78-108, Middle Region
Reactivity
All reactivities for TMIE antibodies
Human
Host
All hosts for TMIE antibodies
Rabbit
Clonality
All clonalities for TMIE antibodies
Polyclonal
Conjugate
All conjugates for TMIE antibodies
This TMIE antibody is un-conjugated
Application
Western Blotting (WB), Enzyme Immunoassay (EIA)
Specificity
This antibody detects TMIE (Center).
Cross-Reactivity (Details)
Species reactivity (tested):Human
Purification
Protein A column followed by peptide affinity purification
Immunogen
KLH conjugated synthetic peptide between 78~108 amino acids from the Central region of human TMIE
Isotype
Ig Fraction
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Discover our top product TMIE Primary Antibody
Alternatives
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Application Details
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Application Notes
Optimal working dilution should be determined by the investigator.
Restrictions
For Research Use only
Handling
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Format
Liquid
Concentration
0.25 mg/mL
Buffer
PBS with 0.09 % (W/V) sodium azide
Preservative
Sodium azide
Precaution of Use
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Handling Advice
Avoid repeated freezing and thawing.
Storage
4 °C/-20 °C
Storage Comment
Store at 2 - 8 °C for up to six months or (in aliquots) at -20 °C for longer.
Target Details for TMIE
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Target
TMIE
(Transmembrane Inner Ear (TMIE))
Alternative Name
TMIE (TMIE Products )
Synonyms
si:ch211-163f10.1 antibody, DFNB6 antibody, 5131400L21Rik antibody, Mm.87012 antibody, sr antibody, RGD1562523 antibody, transmembrane inner ear antibody, tmie antibody, TMIE antibody, Tmie antibody
Background
This gene encodes a transmembrane inner ear protein. Studies in mouse suggest that this gene is required for normal postnatal maturation of sensory hair cells in the cochlea, including correct development of stereocilia bundles. This gene is one of multiple genes responsible for recessive non-syndromic deafness (DFNB), also known as autosomal recessive nonsyndromic hearing loss (ARNSHL), the most common form of congenitally acquired inherited hearing impairment.Synonyms: Transmembrane inner ear expressed protein
Gene ID
259236
NCBI Accession
NP_671729
Pathways
Sensory Perception of Sound
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