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Roche

甲酸脱氢酶

from Candida boidinii

别名:

FDH, 甲酸盐:NAD氧化还原酶

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关于此项目

UNSPSC Code:
12352204
NACRES:
NA.54
Specific activity:
~0.4 units/mg protein (At 25 °C with formate as the substrate.)
Biological source:
yeast (Candida boidini)
Recombinant:
expressed in E. coli
Concentration:
≥10-20 % (w/w)
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产品名称

甲酸脱氢酶, from Candida boidinii

biological source

yeast (Candida boidini)

recombinant

expressed in E. coli

form

lyophilized

specific activity

~0.4 units/mg protein (At 25 °C with formate as the substrate.)

mol wt

74 kDa

packaging

pkg of 250 U (10837016001)
pkg of 80 U (10244678001)

manufacturer/tradename

Roche

concentration

≥10-20 % (w/w)

technique(s)

activity assay: suitable

color

off-white

optimum pH

7.5-8.5

solubility

water: soluble 10 g/L

suitability

suitable for gel electrophoresis

UniProt accession no.

application(s)

life science and biopharma

foreign activity

ADH <0.0500%
LDH <0.0500%
MDH <0.1000%

storage temp.

2-8°C

Quality Level

Analysis Note

污染物:<0.005%的LDH和ADH,<0.1%的MDH

Application

最常用于NADH的辅因子再循环系统。

Biochem/physiol Actions

底物特异性和Km
甲酸脱氢酶仅与甲酸盐(在30℃和pH 7.5条件下,Km = 13 mM;在25℃和pH 7.5条件下,11mM)和NAD(在30℃和pH 7.5条件下,Km 0.09 mM)反应。它不与乙酸盐、草酸盐、乳酸盐、琥珀酸盐、丙酸盐或抗坏血酸盐反应,也不会还原NADP。

General description

甲酸盐:NAD + 氧化还原酶
甲酸脱氢酶是左旋体特异性2-羟基酸脱氢酶超家族的成员。它是由两个相同亚基组成的二聚体。该酶具有一个半胱氨酸残基,它对于酶的活性或结构完整性至关重要。

Other Notes

一单位(U)甲酸脱氢酶在+25 °C、pH 7.6下将1 μmol甲酸氧化成CO2。上述测定中,每氧化1 mmol甲酸将产生1mmol NADH。
仅用于生命科学研究。不可用于诊断。

Preparation Note

干燥储存

存储类别

11 - Combustible Solids

wgk

WGK 2

flash_point_f

does not flash

flash_point_c

does not flash

法规信息

常规特殊物品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Katja Schirwitz et al.
Protein science : a publication of the Protein Society, 16(6), 1146-1156 (2007-05-26)
The understanding of the mechanism of enzymatic recovery of NADH is of biological and of considerable biotechnological interest, since the essential, but expensive, cofactor NADH is exhausted in asymmetric hydrogenation processes, but can be recovered by NAD(+)-dependent formate dehydrogenase (FDH).
Knut Erik Hovda et al.
Scandinavian journal of clinical and laboratory investigation, 75(7), 610-614 (2015-07-24)
The standard diagnostic approach to methanol poisoning is chromatographic measurement of methanol on centrally placed stationary equipment. Methanol poisoning in places where such equipment is unavailable is thus often not diagnosed. Methanol is metabolized to a toxic metabolite, formate; the

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