Human Cochlin (COCH) Protein

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Description
Human Cochlin Protein is a recombinant protein from Human produced in HEK293 Cells. A DNA sequence encoding the mature form of human COCH (NP_001128530.1) (Glu 25-Gln 550) was expressed, with a polyhistidine tag at the N-terminus.
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Product specifications
Category | Proteins and Peptides |
Immunogen Target | Cochlin |
Host | HEK293 cells |
Origin | Human |
Observed MW | Molecular Weight: 59.4 kDa Sequence Fragment: Glu25-Gln550 Tag: N-terminal His tag Validity: The validity for this protein is 12 months. |
Expression | Recombinant |
Purity | > 92% (SDS-PAGE) |
Size 1 | 50 µg |
Size 2 | 100 µg |
Tested Applications | SDS-PAGE |
Buffer | Lyophilized from sterile PBS, pH 7.4. |
Availability | Shipped within 5-15 working days. |
Storage | Aliquot and store at -20°C or -80°C. Avoid repeated freeze/thaw cycles. |
Dry Ice | No |
NCBI Accession | NP_001128530.1 |
Background | Protein COCH |
Status | RUO |
Note | This product is for research use only. Not for human consumption, cosmetic, therapeutic or diagnostic use. |
Descripción
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The protein encoded by this gene is highly conserved in human, mouse, and chicken, showing 94% and 79% amino acid identity of human to mouse and chicken sequences, respectively. Hybridization to this gene was detected in spindle-shaped cells located along nerve fibers between the auditory ganglion and sensory epithelium. These cells accompany neurites at the habenula perforata, the opening through which neurites extend to innervate hair cells. This and the pattern of expression of this gene in chicken inner ear paralleled the histologic findings of acidophilic deposits, consistent with mucopolysaccharide ground substance, in temporal bones from DFNA9 (autosomal dominant nonsyndromic sensorineural deafness 9) patients. Mutations that cause DFNA9 have been reported in this gene. Alternative splicing results in multiple transcript variants encoding the same protein. Additional splice variants encoding distinct isoforms have been described but their biological validities have not been demonstrated. [provided by RefSeq].
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