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Item No. 31606

Provide batch numbers separated by commas to download or request available product inserts, QC sheets, certificates of analysis, data packs, and GC-MS data.

Discover high-quality research tools to investigate GLP-1 mechanisms and next-generation metabolic targets.
OBESITY RESEARCH SOLUTIONSHyodeoxycholic acid (HDCA) is a secondary bile acid.1 It is produced from lithocholic acid (Item No. 20253) by gut bacteria.1,2,3 Dietary administration of HDCA (1.25% w/w) decreases plasma VLDL and LDL cholesterol levels and reduces fasting glucose levels and atherosclerotic lesion size in LDL receptor knockout mice fed a Western diet.4 Serum levels of HDCA are increased in patients with Crohn’s disease or ulcerative colitis.5
Hyodeoxycholic acid MaxSpec® standard is a quantitative grade standard of Hyodeoxycholic Acid (Item No. 20294) that has been prepared specifically for mass spectrometry and related applications where quantitative reproducibility is required. The solution has been prepared gravimetrically and is supplied in a deactivated glass ampule sealed under argon. The concentration was verified by comparison to an independently prepared calibration standard. The verified concentration is provided on the certificate of analysis. This hyodeoxycholic acid MaxSpec® standard is guaranteed to meet identity, purity, stability, and concentration specifications and is provided with a batch-specific certificate of analysis. Ongoing stability testing is performed to ensure the concentration remains accurate throughout the shelf life of the product. Note: The amount of solution added to the vial is in excess of the listed amount. Therefore, it is necessary to accurately measure volumes for preparation of calibration standards. Follow recommended storage and handling conditions to maintain product quality.
WARNING This product is not for human or veterinary use.
1. On the formation of hyodeoxycholic acid in the rat. Bile acids and steroids 154. The Journal of Biological Chemisty 241(3), 534-539 (1966).
2. Analysis of bile acids in conventional and germfree rats. J. Lipid. Res. 17(2), 107-111 (1976).
3. Intestinal absorption, excretion, and biotransformation of hyodeoxycholic acid in man. J. Lipid. Res. 24(5), 604-613 (1983).
4. Hyodeoxycholic acid improves HDL function and inhibits atherosclerotic lesion formation in LDLR-
5. Serum bile acid profiling reflects enterohepatic detoxification state and intestinal barrier function in inflammatory bowel disease. World J. Gastroenterol. 15(25), 3134-3141 (2009).