ESPN Antibody

Code CSB-PA007827GA01HU
Size $600
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Product Details

Uniprot No.
Target Names
ESPN
Alternative Names
ESPN antibody; DFNB36 antibody; LP2654Espin antibody; Autosomal recessive deafness type 36 protein antibody; Ectoplasmic specialization protein antibody
Raised in
Rabbit
Species Reactivity
Human,Mouse,Rat
Immunogen
Human ESPN
Immunogen Species
Homo sapiens (Human)
Isotype
IgG
Purification Method
Antigen Affinity purified
Concentration
It differs from different batches. Please contact us to confirm it.
Buffer
PBS with 0.1% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
Tested Applications
ELISA,WB
Troubleshooting and FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time
Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.

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Target Background

Function
Multifunctional actin-bundling protein. Plays a major role in regulating the organization, dimension, dynamics and signaling capacities of the actin filament-rich microvilli in the mechanosensory and chemosensory cells. Required for the assembly and stabilization of the stereociliary parallel actin bundles. Plays a crucial role in the formation and maintenance of inner ear hair cell stereocilia. Involved in the elongation of actin in stereocilia. In extrastriolar hair cells, required for targeting MYO3B to stereocilia tips, and for regulation of stereocilia diameter and staircase formation.
Gene References into Functions
  1. A significant inverse correlation was observed between miR-612 and Espin protein expression in melanoma tissues. PMID: 29385671
  2. The utricles were then treated with a gamma-secretase inhibitor, followed by espin or control transduction and histochemistry. Although gamma-secretase inhibition increased the number of HCs, few had stereociliary arrays. In contrast, 46 h after espin1 transduction, a significant increase in hair-bundle-like structures was observed PMID: 26886463
  3. The espin actin-filament-binding site has a major effect on the formation and dynamics of actin bundles. PMID: 24424026
  4. human deafness and vestibular dysfunction co-segregated with either of two frameshift mutations in ESPN. PMID: 15286153
  5. The results further strengthen the causative role of the espin gene in non-syndromic hearing loss and add new insights into espin structure and function. PMID: 15930085
  6. Here, we report a new activity of the espins, one that depends on their enigmatic WH2 domain: the ability to assemble a large actin bundle when targeted to a specific subcellular location. PMID: 16569662
  7. A recessive ESPN mutation causing congenital hearing loss in a Morocan family was reported. PMID: 18973245
  8. Flies with mutations affecting the diaphanous,forked, and CG12026/TMHS genes displayed significant reductions in the amplitude of sound-evoked potentials compared to wild-type flies PMID: 19102128

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Involvement in disease
Deafness, autosomal recessive, 36, with or without vestibular involvement (DFNB36)
Subcellular Location
Cytoplasm, cytoskeleton. Cell projection, stereocilium. Cell projection, microvillus.
Database Links

HGNC: 13281

OMIM: 606351

KEGG: hsa:83715

STRING: 9606.ENSP00000367059

UniGene: Hs.744222

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