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OTOGL rabbit pAb

CAT: 0855-ES14356-01Size: 50 µLDry Ice: NoHazardous: No
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CAT#:0855-ES14356-01Size:50 µL
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Background
The protein encoded by this gene belongs to the otogelin family. This gene is expressed in the inner ear of vertebrates with the highest level of expression seen at the embryonic stage and lowest in adult. Knockdown studies in zebrafish suggest that this gene is essential for normal inner ear function. Mutations in this gene are associated with autosomal recessive deafness. [provided by RefSeq, Dec 2012]
Description
The protein encoded by this gene belongs to the otogelin family. This gene is expressed in the inner ear of vertebrates with the highest level of expression seen at the embryonic stage and lowest in adult. Knockdown studies in zebrafish suggest that this gene is essential for normal inner ear function. Mutations in this gene are associated with autosomal recessive deafness. [provided by RefSeq, Dec 2012],
UniProt
Q3ZCN5
Swiss Prot
Q3ZCN5
Reactivity
Human; Rat; Mouse
Immunogen
Synthesized peptide derived from human OTOGL AA range: 584-634
Target
OTOGL
Clonality
Polyclonal
Source
Rabbit
Applications
WB
Concentration
1 mg/ml
Dilution
WB 1:500-2000
Buffer
-20°C/1 year
Storage Conditions
-20°C/1 year
Fragment
IgG
Subcellular Location
Secreted .

UniProtKB · Q3ZCN5

Otogelin-like protein

OTOGL_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q3ZCN5
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
OTOGL
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
Precursor
Secondary accessions
F8W0C3, Q495U8, Q8N8G5, Q8NC28
Protein keywords

Disease

DeafnessNon-syndromic deafness

PTM

Disulfide bondGlycoprotein

Technical term

Proteomics identificationReference proteome

Domain

RepeatSignal

Cellular component

Secreted

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