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USH1C Antibody

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Western Blot: USH1C Antibody [NB100-1405] - (0.1ug/ml) staining of HEK293 lysate (35ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.

Product Details

Summary
Reactivity Hu, Mu, RtSpecies Glossary
Applications WB, ELISA
Clonality
Polyclonal
Host
Goat
Conjugate
Unconjugated
Concentration
0.5 mg/ml

Order Details

USH1C Antibody Summary

Immunogen
Peptide with sequence DRKVAREFRHKVD-C corresponding to N-Terminus according to NP_710142.1.
Localization
Nuclear
Specificity
This antibody is expected to recognize both reported isoforms (NP_005700.2 and NP_710142.1).
Predicted Species
Mouse (100%), Rat (100%). Backed by our 100% Guarantee.
Isotype
IgG
Clonality
Polyclonal
Host
Goat
Gene
USH1C
Purity
Immunogen affinity purified
Innovator's Reward
Test in a species/application not listed above to receive a full credit towards a future purchase.

Applications/Dilutions

Dilutions
  • ELISA Detection limit 1:128000
  • Western Blot 0.1 - 0.3 ug/ml
Application Notes
WB: Approx. 75 kDa band observed in HEK293 lysates (calculated MW of 62.2 kDa band according to NP_005700.2).
Control
293 Whole Cell Lysate
Publications
Read Publications using
NB100-1405 in the following applications:

  • WB
    1 publication

Reactivity Notes

Bovine reactivity reported in scientific literature (PMID: 20058854).

Packaging, Storage & Formulations

Storage
Store at -20C. Avoid freeze-thaw cycles.
Buffer
Tris saline (20 mM Tris pH 7.3, 150 mM NaCl), 0.5% BSA
Preservative
0.02% Sodium Azide
Concentration
0.5 mg/ml
Purity
Immunogen affinity purified

Alternate Names for USH1C Antibody

  • AIE75
  • AIE-75
  • Antigen NY-CO-38/NY-CO-37
  • Autoimmune enteropathy-related antigen AIE-75
  • deafness, autosomal recessive 18
  • DFNB18
  • harmonin
  • NY-CO-37
  • NY-CO-38
  • PDZ-45
  • PDZ73
  • PDZ-73
  • PDZ-73/NY-CO-38
  • Protein PDZ-73
  • Renal carcinoma antigen NY-REN-3
  • ush1cpst
  • Usher syndrome 1C (autosomal recessive, severe)
  • Usher syndrome type-1C protein

Background

USH1C may be involved in protein-protein interaction. Defects in USH1C are the cause of Usher syndrome type 1c. It is an autosomal recessive sensory defect involving congenital profound sensorineural deafness, vestibular dysfunction, and blindness due to progressive retinitis pigmentosa. Defects in USH1C are also the cause of nonsyndromic recessive deafness.

Limitations

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

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Publications for USH1C Antibody (NB100-1405)(2)

We have publications tested in 1 confirmed species: Bovine.

We have publications tested in 1 application: WB.


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WB
(1)
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Filter By Species
Bovine
(1)
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Product General Protocols

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Video Protocols

WB Video Protocol

FAQs for USH1C Antibody (NB100-1405) (0)

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Control Lysate(s)

Secondary Antibodies

 

Isotype Controls

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Bioinformatics

Gene Symbol USH1C
Entrez
Uniprot