Comparison

THYROID PEROXIDASE

Item no. 20-783-73694
Manufacturer GENWAY
Amount 0.2 mg
Category
Type Antibody
Applications WB, ELISA
Clone 6H7
Specific against other
ECLASS 10.1 32160702
ECLASS 11.0 32160702
UNSPSC 12352203
Alias GWB-200826
Similar products 20-783-73694
Available
Genway ID:
GWB-200826
Specificity:
THYROID PEROXIDASE
Specificity:
THYROID PEROXIDASE
Clone:
6H7
Immunogen:
Human thyroid peroxidase
Specificity Note:
This product is specific for human thyroid peroxidase. Thyroid peroxidase (TPO) is an enzyme expressed in the thyroid gland which is necessary for the production of thyroid hormes such as thyroxine. Congenital hypothyroidism and congenital goiter are both associated with mutations in the TPO gene.
Preparation:
Purified IgG prepared by affinity chromatography on Protein A
Buffer Solution:
Phosphate buffered saline pH 7. 2
Preservative Stabilisers:
0. 09%Sodium Azide (NaN3) Summary: This protein is a membrane-bound glycoprotein. The encoded protein acts as an enzyme and plays a central role in thyroid gland function. The protein functions in the iodination of tyrosine residues in thyroglobulin and phenoxy-ester formation between pairs of iodinated tyrosines to generate the thyroid hormones thyroxine and triiodothyronine. Mutations in this gene are associated with several disorders of thyroid hormonogenesis including congenital hypothyroidism congenital goiter and thyroid hormone organification defect IIA. Multiple transcript variants encoding distinct isoforms have been identified for this gene. Additional splice variants have been described but their biological natures have not been determined. Summary: This protein is a membrane-bound glycoprotein. The encoded protein acts as an enzyme and plays a central role in thyroid gland function. The protein functions in the iodination of tyrosine residues in thyroglobulin and phenoxy-ester formation between pairs of iodinated tyrosines to generate the thyroid hormones thyroxine and triiodothyronine. Mutations in this gene are associated with several disorders of thyroid hormonogenesis including congenital hypothyroidism congenital goiter and thyroid hormone organification defect IIA. Multiple transcript variants encoding distinct isoforms have been identified for this gene. Additional splice variants have been described but their biological natures have not been determined. [provided by RefSeq].

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 0.2 mg
Available: In stock
available

Delivery expected until 8/30/2024 

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