Hai cercato: Magnesium+trisilicate,+hydrate

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Calcium glycerophosphate hydrate 97%

Fornitore: Thermo Fisher Scientific

Descrizione: Calcium glycerophosphate hydrate 97%

MSDS

Iron(III) phosphate hydrate

Fornitore: Thermo Fisher Scientific

Descrizione: Iron(III) phosphate hydrate

MSDS Certificati

1-Benzylpiperidin-3-one hydrochloride hydrate, idrato

Fornitore: Thermo Fisher Scientific

Descrizione: 1-Benzylpiperidin-3-one hydrochloride hydrate, idrato

MSDS Certificati

2,4-Difluorophenylglyoxal hydrate 95% (dry weight)

Fornitore: Thermo Fisher Scientific

Descrizione: 2,4-Difluorophenylglyoxal hydrate 95% (dry weight)

MSDS Certificati

4-Hydrazinobenzenesulphonic acid hydrate 98%

Fornitore: Thermo Fisher Scientific

Descrizione: 4-Hydrazinobenzenesulphonic acid hydrate 98%

MSDS Certificati

6-Acetamidohexanoic acid hydrate 99%

Fornitore: Thermo Fisher Scientific

Descrizione: 6-Acetamidohexanoic acid hydrate 99%

MSDS Certificati

4-Hydroxyphenylglyoxal hydrate 95%

Fornitore: Apollo Scientific

Descrizione: 4-Hydroxyphenylglyoxal hydrate 95%

(±)Catechin hydrate, off-white powder

Fornitore: Apollo Scientific

Descrizione: (±)Catechin hydrate, off-white powder

Anti-FAHD2A Rabbit Polyclonal Antibody

Codice catalogo: (BOSSBS-8228R)

Fornitore: Bioss

Codice articolo fornitore: BS-8228R

Codice articolo locale: BOSSBS-8228R

Descrizione: The FAH family contains two highly homologous 314 amino acid proteins, designated FAHD2A (fumarylacetoacetate hydrolase domain-containing protein 2A) and FAHD2B (fumarylacetoacetate hydrolase domain-containing protein 2A). FAHD2A and B utilize calcium and magnesium as cofactors, and may possess hydrolase activity. The genes encoding FAHD2A/B map to human chromosome 2, the second largest human chromosome, which consists of 237 million bases, encodes over 1,400 genes and makes up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstré°‰ syndrome, is also associated with mutations to chromosome 2.

UOM: 1 * 100 µl

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