USH1C Antibody (2B3) - Azide and BSA Free

Western Blot: USH1C Antibody (2B3) [H00010083-M07] - Analysis of USH1C transfected lysate using anti-USH1C monoclonal antibody and Protein A Magnetic Bead, and immunoblotted with USH1C monoclonal antibody.

Western Blot: USH1C Antibody (2B3) [H00010083-M07] - Analysis of USH1C expression in transfected 293T cell line by USH1C monoclonal antibody (M07), clone 2B3. Lane 1: USH1C transfected lysate (Predicted MW: 60.3 KDa). Lane 2: Non-transfected lysate.

• Reactivity: Hu
• Applications: WB, ELISA, IP
• Clone: 2B3
• Clonality: Monoclonal
• Host: Mouse
• Conjugate: Unconjugated
• Format: Azide and BSA Free

USH1C Antibody (2B3) - Azide and BSA Free Summary

• Description: Novus Biologicals Mouse USH1C Antibody (2B3) - Azide and BSA Free (H00010083-M07) is a monoclonal antibody validated for use in WB, ELISA and IP. All Novus Biologicals antibodies are covered by our 100% guarantee.
• Immunogen: USH1C (AAH16057, 424 a.a. ~ 533 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa. FTPEQIMGKDVRLLRIKKEGSLDLALEGGVDSPIGKVVVSAVYERGAAERHGGIVKGDEIMAINGKIVTDYTLAEADAALQKAWNQGGDWIDLVVAVCPPKEYDDELTFF
• Specificity: USH1C - Usher syndrome 1C (autosomal recessive, severe) (2B3)
• Isotype: IgG2a Kappa
• Clonality: Monoclonal
• Host: Mouse
• Gene: USH1C
• Purity: IgG purified

Applications/Dilutions

• Dilutions:
  • ELISA
  • Immunoprecipitation
  • Western Blot
• Application Notes: This antibody is useful for ELISA.

Packaging, Storage & Formulations

• Storage: Aliquot and store at -20C or -80C. Avoid freeze-thaw cycles.
• Buffer: In 1x PBS, pH 7.4
• Preservative: No Preservative
• Purity: IgG purified

Notes

This product is produced by and distributed for Abnova, a company based in Taiwan.

Alternate Names for USH1C Antibody (2B3) - Azide and BSA Free

• 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.

Bioinformatics

• Gene Symbol: USH1C
• Entrez:
  • 10083(Human)
• Uniprot:
  • AAH16057(Human)