Harmonin cDNA ORF Clone in Cloning Vector, Human

Cat: HG10613-M
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Harmonin cDNA ORF Clone in Cloning Vector, Human General Information
Gene
Species
Human
NCBI Ref Seq
RefSeq ORF Size
1659 bp
Sequence Description
Identical with the Gene Bank Ref. ID sequence.
Description
Full length Clone DNA of Human Usher syndrome 1C (autosomal recessive, severe), transcript variant 1.
Plasmid
Vector
pMD18-T Simple Vector
Sequencing Primers
M13-47 and RV-M
Quality Control
The plasmid is confirmed by full-length sequencing.
Screening
Antibiotic in E.coli
Ampicillin
Storage & Shipping
Shipping
Each tube contains lyophilized plasmid.
Storage
The lyophilized plasmid can be stored at ambient temperature for three months.
Harmonin cDNA ORF Neucleotide Sequence and Amino Acid Sequence Information

**Sino Biological guarantees 100% sequence accuracy of all synthetic DNA constructs we deliver, but we do not guarantee protein expression in your experimental system. Protein expression is influenced by many factors that may vary between experiments or laboratories.**

Harmonin cDNA ORF Clone in Cloning Vector, Human Alternative Names
AIE-75 cDNA ORF Clone, Human;DFNB18 cDNA ORF Clone, Human;DFNB18A cDNA ORF Clone, Human;NY-CO-37 cDNA ORF Clone, Human;NY-CO-38 cDNA ORF Clone, Human;PDZ-45 cDNA ORF Clone, Human;PDZ-73 cDNA ORF Clone, Human;PDZ-73/NY-CO-38 cDNA ORF Clone, Human;PDZ73 cDNA ORF Clone, Human;PDZD7C cDNA ORF Clone, Human;ush1cpst cDNA ORF Clone, Human
Harmonin Background Information

Harmonin, also known as Antigen NY-CO-38 / NY-CO-37, Autoimmune enteropathy-related antigen AIE-75, Protein PDZ-73, Renal carcinoma antigen NY-REN-3, Usher syndrome type-1C protein and USH1C, is a protein which is expressed in small intestine, colon, kidney, eye and weakly in pancreas. USH1C is expressed also in vestibule of the inner ear. USH1C contains 3 PDZ (DHR) domains. USH1C may be involved in protein-protein interaction. Defects in USH1C are the cause of Usher syndrome type 1C (USH1C), also known as Usher syndrome type I Acadian variety. USH is a genetically heterogeneous condition characterized by the association of retinitis pigmentosa and sensorineural deafness. Age at onset and differences in auditory and vestibular function distinguish Usher syndrome type 1 (USH1), Usher syndrome type 2 (USH2) and Usher syndrome type 3 (USH3). Defects in USH1C are also the cause of deafness autosomal recessive type 18 (DFNB18) which is a form of sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information.

Full Name
Usher syndrome 1C (autosomal recessive, severe)
References
  • Verpy, E. et al., 2000, Nat Genet. 26 (1):51-5.
  • Weil D., et al., 2003, Hum. Mol. Genet. 12:463-471.
  • Reiners,J. et al., 2005, Hum Mol Genet. 14 (24):3933-43.
  • Yan,D. et al., 2006, Mol Biol. 357 (3):755-64.
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    Harmonin cDNA ORF Clone, Human, Related Products

    Product Name Catalog#(PDF)
    Harmonin cDNA ORF Clone, Human, untagged HG10613-UT
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    Harmonin Lentiviral cDNA ORF Clone, Human, C-GFPSpark® tag HG10613-ACGLN
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    Harmonin cDNA ORF Clone, Human, N-DDK (Flag®) tag HG10613-NF
    Harmonin cDNA ORF Clone, Human, C-His tag HG10613-CH
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    Harmonin cDNA ORF Clone, Human, C-Myc tag HG10613-CM
    Harmonin cDNA ORF Clone, Human, N-Myc tag HG10613-NM
    Harmonin qPCR Primer Pairs, Human HP100863
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