Anti-Thyroid Peroxidase polyclonal antibody (DPABH-22989)

Specifications


Host Species
Goat
Antibody Isotype
IgG
Species Reactivity
Human
Immunogen
Synthetic peptide: C-TRHVIQVSNEVVTDD with a Cysteine residue linker, corresponding to internal sequence amino acids 209-223 of Human Thyroid Peroxidase (NP_000538.3; NP_783650.1; NP_783652.1; NP_783653.1).
Conjugate
Unconjugated

Applications


Application Notes
WB: 0.3 - 1 μg/ml. IHC-P: 5 - 10 μg/ml.
*Suggested working dilutions are given as a guide only. It is recommended that the user titrates the product for use in their own experiment using appropriate negative and positive controls.

Target


Alternative Names
TPO; thyroid peroxidase; MSA; TPX; TDH2A; thyroperoxidase
Entrez Gene ID
UniProt ID

Product Background


Pathway
Amine-derived hormones; Autoimmune thyroid disease; Cytokine-cytokine receptor interaction; Hematopoietic cell lineage

Citations


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We offer labeled antibodies using our catalogue antibody products and a broad range of intensely fluorescent dyes and labels including HRP, biotin, ALP, Alexa Fluor® dyes, DyLight® Fluor dyes, R-phycoerythrin (R-PE), at scales from less than 100 μg up to 1 g of IgG antibody. Learn More

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References


Genome-Wide Analysis Identifies Two Susceptibility Loci for Positive Thyroid Peroxidase and Thyroglobulin Antibodies

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Authors: Matana, Antonela; Boutin, Thibaud; Torlak, Vesela; Brdar, Dubravka; Gunjaca, Ivana; Kolcic, Ivana; Perica, Vesna Boraska; Punda, Ante; Polasek, Ozren; Barbalic, Maja; Hayward, Caroline; Zemunik, Tatijana

Introduction: Thyroid peroxidase (TPO) and thyroglobulin (Tg) are main components of the thyroid gland and play an essential role in thyroid hormone synthesis. The development of antibodies to thyroid peroxidase (TPOAb) and thyroglobulin (TgAb) is the major diagnostic hallmark and early indicator of autoimmune thyroid disease. TPOAb and TgAb are under strong genetic influence; however, genetic factors that determine thyroid antibody positivity are largely unknown. Materials and Methods: To identify novel loci associated with TPOAb and/or TgAb positivity, we performed a genome-wide meta-analysis in a total of 2613 individuals from Croatia. Participants with elevated plasma TPOAb and/or TgAb were defined as cases (N = 619) and those with TPOAb and TgAb within reference values were defined as controls (N = 1994). Results: We identified 2 novel loci, of which 1 is located within the YES1 gene (rs77284350, P = 1.50 x 10(-8)), and the other resides within the IRF8 gene (rs16939945, P = 5.04 x 10(-8)). Conclusions: Although the observed variants were associated with TPOAb and TgAb positivity for the first time, both YES1 and IRF8 were previously linked to susceptibility to other autoimmune diseases, and represent plausible biological candidates. This study adds to the knowledge of genetics underlying thyroid antibodies and provides a good basis for further research.

Bimetallic BaFe2MAl9O19 (M = Mn, Ni, and Co) hexaaluminates as oxygen carriers for chemical looping dry reforming of methane

APPLIED ENERGY

Authors: Zhu, Yanyan; Jin, Nannan; Liu, Ruilin; Sun, Xueyan; Bai, Lei; Tian, Hanjing; Ma, Xiaoxun; Wang, Xiaodong

Chemical looping dry reforming of methane allows the continuous production of syngas and CO with decreased carbon footprint from two separated reactors, which provided system flexibility for various downstream applications, such as F-T synthesis or hydrogen purification. A key issue for this process is to find an appropriate oxygen carrier (OC) with high reactivity and recyclability. In this work, bimetallic BaFe2MAl9O19 (M = Mn, Ni, and Co) hexaaluminates were studied as OCs, with Fe-substituted BaFe2Al10O19 and BaFe3Al9O19 for comparison. The influence of Mn, Ni, and Co doping on structure, redox reactivity and stability was investigated by means of XRD, XPS, BET, H-2-TPR, CH4-IR, SEM, CO2-TPO and fixed-bed experiments. Pure Fe-substituted OCs presented the coexistence of beta-Al2O3 and magnetoplumbite (MP) hexaaluminate phases, which transformed from MP to beta-Al2O3 during cyclic CH4/CO2 operation. Bimetallic BaFe2MAl9O19 (M = Mn, Ni, and Co) only crystallized in beta-Al2O3 hexaaluminate due to the presence of +2 valent Mn, Ni, and Co, and the beta-Al2O3 structure still remained stable during the CH4 reduction step. Mn doping inhibited the release of lattice oxygen, while Ni doping initiated significant CH4 pyrolysis. Among all dopants, the BaFe2CoAl9O19 OC exhibited good reactivity for syngas production with high CH4 conversion, high syngas yield, desirable H-2/CO ratio (similar to 2), and stable regenerability by CO2, taking advantages of the enhanced oxygen-donation ability and the preservation of hexaaluminate phase during successive CH4/CO2 redox cycles.

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