Protein Tyrosine Phosphatase Receptor Type Q (PTPRQ) Antibody

Este producto es parte de PTPR - protein tyrosine phosphatase receptor type
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286€ (100 µl)

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935106861
info@markelab.com
name
Protein Tyrosine Phosphatase Receptor Type Q (PTPRQ) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx129111
tested applications
WB, IHC, IF/ICC

Description

Protein Tyrosine Phosphatase Receptor Type Q Antibody is a Rabbit Polyclonal against Protein Tyrosine Phosphatase Receptor Type Q.

Documents del producto

Instrucciones
Data sheet
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Product specifications

CategoryPrimary Antibodies
Immunogen TargetProtein Tyrosine Phosphatase Receptor Type Q (PTPRQ)
HostRabbit
ReactivityHuman
Recommended DilutionWB: 0.01-2 µg/ml, IHC: 5-20 µg/ml, IF/ICC: 5-20 µg/ml. Optimal dilutions/concentrations should be determined by the end user.
ClonalityPolyclonal
ConjugationUnconjugated
PurificationPurified by antigen-specific affinity chromatography, followed by Protein A affinity chromatography.
Size 1100 µl
Size 2200 µl
Size 31 ml
FormLiquid
Tested ApplicationsWB, IHC, IF/ICC
Buffer0.01 M PBS, pH 7.4, containing 0.05% Proclin-300, 50% glycerol.
AvailabilityShipped within 5-7 working days.
StorageAliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry IceNo
UniProt IDQ9UMZ3
AliasDFNA73,DFNB84,DFNB84A,PTPGMC1,R-PTP-Q,Receptor-type tyrosine-protein phosphatase Q,Phosphatidylinositol phosphatase PTPRQ
BackgroundAntibody anti-PTPRQ
StatusRUO
NoteConcentration: 0.31 mg/ml -

Descripción

PTPRQ is a receptor-like protein tyrosine phosphatase that plays critical roles in hair cell function, auditory processes, and cellular signaling. Structurally, PTPRQ contains extracellular domains, a single transmembrane region, and an intracellular phosphatase domain with enzymatic activity. It is primarily expressed in sensory hair cells of the inner ear, where it regulates the structure and function of stereocilia, specialized actin-rich projections responsible for mechanotransduction. PTPRQ is essential for maintaining hair cell integrity and hearing function by modulating phosphatidylinositol signaling and dephosphorylating key targets. Mutations in PTPRQ are associated with autosomal recessive non-syndromic hearing loss, underscoring its importance in auditory physiology. Beyond the ear, PTPRQ also contributes to cellular adhesion, signaling, and cytoskeletal dynamics. Its dysfunction highlights its role in sensory processes and cellular regulation.

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