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Recommended positive controls: 293T, A431, H1299, HeLaS3, HepG2, Molt-4, Raji.
Predicted reactivity: Mouse (100%), Rat (100%), Bovine (100%).
Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.
Retinoic acid (RA) represents the oxidized form of vitamin A and, via interactions with retinoic acid receptors (RARs), plays a crucial role in development, cellular growth and differentiation. The gene encoding RAI15 maps to human chromosome 2, which houses over 1,400 genes and comprises nearly 8% of the human genome. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene, while the lipid metabolic disorder sitosterolemia is associated with defects in the ABCG5 and ABCG8 genes. Additionally, an extremely rare recessive genetic disorder, Alström syndrome, is caused by mutations in the ALMS1 gene, which maps to chromosome 2.
⚠WARNING: This product can expose you to chemicals including mercury, which is known to the State of California to cause birth defects or other reproductive harm. For more information go to www.P65Warnings.ca.gov.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: [histone H4]-lysine20 N-trimethyltransferase SMYD5; Histone-lysine N-trimethyltransferase SMYD5; Protein NN8 4AG; Protein NN8-4AG; retinoic acid induced 15; retinoic acid responsive; retinoic acid responsive gene 1; Retinoic acid-induced protein 15; SET and MYND domain-containing protein 5
基因别名: AW536703; NN8-4AG; RAI15; RRG1; SMYD5; ZMYND23
UniProt ID: (Human) Q6GMV2, (Mouse) Q3TYX3
Entrez Gene ID: (Human) 10322, (Mouse) 232187