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G1492

Manufactured by Solarbio
Sourced in China

G1492 is a laboratory equipment product. It serves a core function, but a detailed description while maintaining an unbiased and factual approach is not available.

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5 protocols using g1492

1

Quantifying Osteoclast Activity via TRAP

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TRAP staining was carried out according to the manufacturer’s instructions (G1492, Solarbio, Beijing, China). The area of the callus was defined as the region of interest. TRAP-positive cells were counted using image analysis software.22 (link)
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2

Osteoclast Density Evaluation in Bone Callus

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The same steps (see “Histological analysis” section) were taken to process the slices, and then Tartrate-resistant acid phosphatase (TRAP) staining was performed to evaluate the density of osteoclasts in the callus area following a standard protocol (G1492, Solarbio, Beijing, China). Measurement processes were performed as previously described [19 (link)].
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3

Bone metabolism evaluation protocol

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Medicine refrigerator (BYC-310, Shandong Boke Biology), refrigerated freezer (BD/BC-415DKEM, Midea), slicer (BQ-318D, Bernard), electric blast drying oven (HGZF-101-1, Shanghai Yuejin Medical Instruments Co., Ltd.), thermostatic incubator (DHP-9054, Shandong Boke Biology), electric thermostatic incubator (DHP-9054, Shandong Boke Biology Industry Co., Ltd.); Pressure cooker (YS20ED, Suber), induction cooker (HK-22, Hanke Electric Appliance Factory, Dongfeng Town, Zhongshan City), fume hood; Microscope (CX43, OLYMPUS), microtome (2235, Leica), multifunctional enzyme marker (SuPerMax 3100, flash spectrum); First antibody: BMP-2 (AF5163, Affinity); leptin(DF8583, Affinity); Sema4d (PAB430Ra01, cloud clone); Second antibody: horseradish enzyme-labeled goat anti-rabbit IgG (H + L) (ZB-2301, Zhongshan Jinqiao, 1/100); Tartrate-resistant acid phosphatase staining solution (G1492, Solarbio); Rat tartrate-resistant acid phosphatase 5b (TRACP-5b) ELISA reagent (MM-70644R1, enzyme immunoassay); Rat bone alkaline phosphatase (BALP) kit (MM-0619R1, enzyme immunoassay); Melatonin (S20287) was purchased from Shanghai Yuanye Biotechnology Co., Ltd., with a relative molecular weight of 232.28 and a purity of more than 99%.
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4

Histological Analysis of Bone Sections

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Hydrated bone sections were stained for hematoxylin and eosin staining (Solarbio, G1120), TRAP staining (Solarbio, G1492) and Safranin O/Fast green staining (Solarbio, G1371) according to the manufacturer’s directions, and analyzed by the Bioquant Osteo software (Bioquant Image Analysis Corp, USA).
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5

Quantifying Osteoclast Activity and Mineralization

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Cell plates or histological sections were stained with a tartrate‐resistant acid phosphatase (TRAP) staining solution (G1492‐4 × 20 mL, Solarbio, Beijing, China) for 40 min (cell plate) or 20 min (slides) followed by hematoxylin or methyl green following the manufacturer's instructions. Positive multinucleated osteoclasts (≥3 nuclei) were observed and counted.13, 33 Immunohistochemically stained slices from the proximal epiphyses and growth plates of the proximal tibiae were analyzed.13, 22 The osteoclast numbers and osteoclast surface areas were assessed using ImageJ (USA). Alkaline phosphatase (ALP) staining (C3206, Beyotime, Haimen, China) and staining of mineralized nodules with alizarin red (G1452, Solarbio, Beijing, China) were performed following the manufacturers' instructions. The proximal tibiae were analyzed using a 1500×1800‐μm region of interest (ROI) 150 μm from the growth plate in a grid‐like pattern along the ROI.34 Five fields of each slide and five slides were randomly selected for analysis.35
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