Recombinant Human Usher Syndrome 1C

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Catalog number: GWB-617216
Price: 564 €
Supplier: MBS Polyclonals_1
Product name: Recombinant Human Usher Syndrome 1C
Quantity: 100ul
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Available sizes: 1000ug:3553, 20ug:182, 5ug:83
Old catalog number: 10-663-46733
Store: store in freezer for long therm or fridge for short time storage
Category: Coli rec, ELISAs, e, human proteins, research antibodies
Properties: Depending on the epitopes used human ELISA kits can be cross reactive to many other species, Mainly analyzed are human serum, Modern , cDNA and human recombinants are used in human reactive ELISA kits and to produce anti-human mono and polyclonal antibodies, human cell culture supernatants and biological samples, plasma, primarily , saliva, urine,  , (Homo sapiens, Homo sapiens sapiens), Human proteins, humans , ssp
Source: proteins, Recombinants or rec
Group: recombinants
Gene target: Usher Syndrome 1C
Short name: Recombinant Usher Syndrome 1C
Technique: E, coli recombinant proteins are , genways bulk advises they will be reconstituted in a buffer soluion or culture medium for cell culture, supplied as white sterile powder lyopillized, Recombinant, genetic recombinations , in Escherichia coli
Species: Humans, Human
Alternative name: sapiens Usher Syndrome 1C, recombinant H
Alternative technique: rec
Identity: 2824
Gene: DFNB18 | More about : DFNB18
Long gene name: USH1 protein network component harmonin
Synonyms gene name: autosomal recessive 18 Usher syndrome 1C (autosomal recessive, deafness, severe) Usher syndrome 1C
Synonyms: PDZ73 harmonin NY-CO-37 NY-CO-38 PDZ-73 AIE-75 PDZD7C USH1C
Synonyms name: harmonin
Locus: 11p15, 1
Discovery year: 1992-06-08
GenBank acession: AB006955
Entrez gene record: 10083
Pubmed identfication: 10973247 12107438
RefSeq identity: NM_005709
Classification: Deafness associated genes PDZ domain containing
Havana BLAST/BLAT: OTTHUMG00000166323
Locus Specific Databases: Mutations of the Harmonin Gene CCHMC-BMI &, UC Hearing Loss Mutation Database

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