Recombinant Human Pendrin (SLC26A4) (H723R) Protein, Homo sapiens (Human), in vitro E.coli expression system, N-terminal 6xHis-tagged, 86.7kDa, purity >85% as determined by SDS-PAGE.

Recombinant Human Pendrin (SLC26A4) (H723R) Protein

Recombinant Human Pendrin (SLC26A4) (H723R) Protein — Sodium-independent transporter of chloride and iodide. Purity >85%.

SKU: BCRECP-00433TM Category:
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Product Specifications

Uniprot No.O43511
Gene NamesSLC26A4
PurityGreater than 85% as determined by SDS-PAGE.
Expression Systemin vitro E.coli expression system
Expression Region1-780aa(H723R)
SpeciesHomo sapiens (Human)
Tag InfoN-terminal 6xHis-tagged
Molecular weight86.7kDa
BufferIf the delivery form is liquid, the default storage buffer is Tris/PBS-based buffer, 5%-50% glycerol.If the delivery form is lyophilized powder, the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose.
StorageStore at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. Avoid repeated freeze-thaw cycles.

Function

Sodium-independent transporter of chloride and iodide. Mediates electroneutral chloride-bicarbonate, chloride-iodide and chloride-formate exchange with 1:1 stoichiometry. Mediates electroneutral iodide-bicarbonate exchange.

Biological Context

Subcellular Location: Cell membrane (Multi-pass membrane protein); Apical cell membrane (Multi-pass membrane protein)
Tissue Specificity: Highly expressed in the kidney (at protein level). High expression in adult thyroid, lower expression in adult and fetal kidney and fetal brain. Not expressed in other tissues
Disease Association: Pendred syndrome (PDS) : An autosomal recessive disorder characterized by congenital sensorineural hearing loss in association with thyroid goiter. The disorder may account for up to 10% of the cases of hereditary deafness. The deafness is most often associated with a Mondini cochlear defect. Deafness occurs early, starting at birth or during the first years of life. It is bilateral, sometimes asymmetrical, fluctuant and often progressive. Thyroid perturbations, such as thyroid goiter and/or hypothyroidism appear most commonly during adolescence, but they can be congenital or appear later. [The disease is caused by variants affecting the gene represented in this entry] | Deafness, autosomal recessive, 4 (DFNB4) : A form of non-syndromic 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. DFNB4 is associated with an enlarged vestibular aqueduct. [The disease is caused by variants affecting the gene represented in this entry]

Product Specifications

Recombinant Human Pendrin (SLC26A4) (H723R) Protein is a recombinant protein from Homo sapiens (Human), expressed in in vitro E.coli expression system, covering amino acids 1-780aa(H723R), with N-terminal 6xHis-tagged tag, molecular weight 86.7kDa, purity Greater than 85% as determined by SDS-PAGE.. Suitable for ELISA and Western Blot applications.

Recommended applications depend on the target, product format, and product-specific validation data. Refer to the product datasheet or Certificate of Analysis (CoA), or contact BioCrest Sci for application guidance.

Biological Activity: Not implied unless activity data are explicitly listed on this product page, the datasheet, or the CoA.

Storage: Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. Avoid repeated freeze-thaw cycles.

Shipping & Lead Time: Availability, shipping conditions, and estimated lead time are confirmed in the formal quotation or order confirmation based on the product format, destination, and order requirements.

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Protein Biology

Function

Sodium-independent transporter of chloride and iodide (PubMed:10192399, PubMed:11932316, PubMed:12107249, PubMed:16684826, PubMed:24051746). Mediates electroneutral chloride-bicarbonate, chloride-iodide and chloride-formate exchange with 1:1 stoichiometry (PubMed:10644529, PubMed:15155570, PubMed:24051746, PubMed:35601831). Mediates electroneutral iodide-bicarbonate exchange (By similarity)

Subcellular Location

Cell membrane (Multi-pass membrane protein); Apical cell membrane (Multi-pass membrane protein)

Disease Association

Pendred syndrome (PDS) : An autosomal recessive disorder characterized by congenital sensorineural hearing loss in association with thyroid goiter. The disorder may account for up to 10% of the cases of hereditary deafness. The deafness is most often associated with a Mondini cochlear defect. Deafness occurs early, starting at birth or during the first years of life. It is bilateral, sometimes asymmetrical, fluctuant and often progressive. Thyroid perturbations, such as thyroid goiter and/or hypothyroidism appear most commonly during adolescence, but they can be congenital or appear later. [The disease is caused by variants affecting the gene represented in this entry] | Deafness, autosomal recessive, 4 (DFNB4) : A form of non-syndromic 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. DFNB4 is associated with an enlarged vestibular aqueduct. [The disease is caused by variants affecting the gene represented in this entry]

Tissue Specificity

Highly expressed in the kidney (at protein level) (PubMed:11274445). High expression in adult thyroid, lower expression in adult and fetal kidney and fetal brain. Not expressed in other tissues (PubMed:9398842)

Subunit

Interacts with IQGAP1; this interaction enhances the chloride-bicarbonate exchange activity of SLC26A4

Gene: SLC26A4  |  Organism: Homo sapiens  |  Synonyms: Sodium-independent chloride/iodide transporter; Solute carrier family 26 member 4
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Quality-control data such as identity, purity, endotoxin level, or biological activity are provided only when specified on this product page, the datasheet, or Certificate of Analysis (CoA). Biological activity is not implied unless explicitly stated.

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