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Za3300

Manufactured by Hitachi
Sourced in Japan

The Hitachi ZA3300 is a versatile laboratory equipment designed for general analytical applications. It features a compact and durable construction, providing reliable performance in a laboratory setting. The core function of the ZA3300 is to enable accurate and consistent data collection for a variety of research and testing purposes.

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5 protocols using za3300

1

Serum and Bone Mineral Analysis

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Serum zinc was measured using a metallo-assay kit (Metallogenics, Chiba, Japan). Serum calcium and zinc, and bone calcium and iron in femur were analyzed using atomic absorption spectrophotometry (ZA3300, Hitachi, Ltd., Tokyo, Japan) according to the method of Gimblet et al.(19 (link)) Bone phosphorus was analyzed colorimetrically according to the method of Gomori.(20 ) Serum Osteocalcin concentration was measured using an Osteocalcin Rat ELISA System (GE Healthcare UK Ltd., Amersham, England). The serum C-terminal telopeptide of type I collagen (CTx) level was assayed using the RatLaps ELISA (Immunodiagnostic Systems Nordic A/S, Herlev, Denmark).
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2

Serum and Bone Mineral Analysis

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Serum zinc was measured using a metallo-assay kit (Metallogenics, Chiba, Japan). Serum iron was measured using the Fe C-test (Wako Pure Chem. Ind.). Serum magnesium was measured using the Mg B-test (Wako Pure Chem. Ind.). Minerals in other serum and bone samples were analyzed using atomic absorption spectrophotometry (ZA3300, Hitachi, Ltd., Tokyo, Japan) according to the method of Gimblet et al.(24 (link)) Bone phosphorus was analyzed colorimetrically according to the method of Gomori.(25 ) The serum osteocalcin concentration was measured using an Osteocalcin rat ELISA system (GE Healthcare UK Ltd., Amersham, England). The serum C-terminal telopeptide of type I collagen (CTx) level was assayed using the RatLaps ELISA (Immunodiagnostic systems A/S, Herlev, Denmark).
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3

Dietary Phosphate Induced Kidney Mineralization

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Runx2fl/fl and Runx2fl/flCre mice at 3 weeks of age were fed on high phosphate diet (0.5% calcium and 1.0% phosphorus) for 4 weeks, and they were sacrificed at 7 weeks of age. The kidney samples were dried, ashed, and demineralized with 1 mol/L HCl solution. Ca concentration was analyzed by atomic absorption spectrophotometry (ZA3300, Hitachi High-Tech Corp., Tokyo, Japan) according to the method of Gimblet et al. [23 (link)]. P content was measured colorimetrically by the method of Gomori [24 ].
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4

Characterization of AuNP@Cellulose Nanofiber Papers

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The porous structure of AuNP@cellulose nanofiber paper and AuNP@cellulose nanofiber/pulp paper were observed by a field-emission scanning electron microscope (FE-SEM, SU-8020, Hitachi High-Tech Science Corp., Tokyo, Japan). The AuNP contents were determined by an atomic absorption spectrophotometer (ZA3300, Hitachi High-Tech Science Corp., Tokyo, Japan). Transmittance, reflectance and absorbance spectra were measured by a UV-vis-NIR spectrophotometer (UV-3600 Plus, Shimadzu Corp., Kyoto, Japan) with an integrating sphere attachment (ISR-603, Shimadzu Corp., Kyoto, Japan). Absorption spectra were calculated from the transmittance and reflectance spectra as shown in Fig. S3. The X-ray diffraction (XRD) patterns were recorded by an Ultima IV (Rigaku Corp., Tokyo, Japan), with a scanning angle (2θ) range of 5–80°. A digital thickness gauge (G2N-255M, Ozaki MFG. Co., Ltd., Tokyo, Japan) was used for the measurement of the thickness.
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5

Soil Physicochemical Characterization Protocol

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Soil pH was determined in a 1:5 water-soluble extract. Exchangeable Al3+ (exch. Al) was determined by an atomic absorption spectrophotometer (ZA3300, Hitachi, Japan) after 1 M KCl extraction. Total C and N were measured using a dry combustion method with an NC analyzer (SUMIGRAPH NC-TR-22, Sumika Chemical Analysis Service, Ltd., Japan). Inorganic N (NH4+ and NO3) was extracted from 2 g of soil (dry base) with 10 ml of 1 M KCl for 30 min on a shaker, and the suspension was filtered through filter paper (No. 5C, Advantec, Co., Ltd, Japan). NH4+–N in the extract was analyzed using the modified indophenol blue method (Rhine et al., 1998 (link)) with a spectrophotometer (UV-1280, Shimadzu, Co., Ltd., Japan). NO3–N in the extract was analyzed by flow injection analysis using a flow-through visible spectrophotometer (S3250, Soma Optics, Ltd., Japan). All soil measurements were expressed on an oven-dry soil weight basis (105°C, 24 h).
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