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Merck
CN

10745731001

Roche

β-Galactosidase

EIA grade

别名:

β galactosidase, β-galactosidase

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About This Item

UNSPSC代码:
12352204

生物来源

Escherichia coli

质量水平

检测方案

(single peak, HPLC)

形式

lyophilized

比活

750-950 U/mg

分子量

540.000  kDa

包装

pkg of 25 mg (approx. 100 mg lyophilizate)

制造商/商品名称

Roche

技术

enzyme immunoassay: suitable

颜色

white

pH值(酸碱度)

7.3-7.7

溶解性

water: 20 mg/mL

λmax

405

适用性

suitable for immunoassay

NCBI登记号

UniProt登记号

应用

life science and biopharma

运输

dry ice

储存温度

−20°C (−15°C to −25°C)

基因信息

Escherichia coli ... lacZ(945006)

一般描述

β-Galactosidase, EIA grade, is a lyophilizate from E. coli overproducer, consisting of enzyme protein, phosphate buffer, and sucrose. Substances which could interfere with the derivatization of NH2 or SH groups (e.g., 2-mercaptoethanol, ammonium salts, primary amines etc.) have been removed.
The GLB1 (β-Galactosidase) gene is mapped to human chromosome 3p22.3. The encoded protein belongs to glycosyl hydrolase 35 family and is localized to lysosomes.

应用

β-Galactosidase has been used as a standard to determine the absolute quantitation of LacZ protein.
β-Galactosidase is used for labeling enzyme immunoassay techniques. β-Galactosidase can be coupled to other proteins via its SH-groups. The reconstituted solution can be used directly for conjugation without prior dialysis or gel permeation chromatography.

生化/生理作用

β-Galactosidase catalyzes the hydrolysis of terminal β-galactose residue of ganglioside substrates, such as glycoproteins, sphingolipids, and keratan sulfate and other glycoconjugates. This enzyme is associated with the mechanism of cell senescence and carcinogenesis. Mutations in the gene result in gangliosidosis, an autosomal recessive disorder, characterized with defective lysosomal storage due to accumulation of substrates. β-Galactosidase deficiency also causes Morquio B syndrome indicating skeletal abnormalities, short stature and increased excretion of keratan sulfate in urine.

质量

Purity: single peak (HPLC)

序列

Free Thiol Groups
The non-denatured, enzymatically-active preparation contains > 12 SH groups per molecule which are not involved in disulfide bridges and are freely accessible to coupling reagents in aqueous media (as assayed with Ellman′s reagent at +37 °C, acc. to Habeeb, 1972).

Absence of Enzyme Aggregates
The preparation contains < 3% dimers (HPLC, area %) and essentially no higher oligomers.

外形

Lyophilizate, stabilized with phosphate buffer and sucrose. Note: Contains at least 12 free SH-groups/enzyme molecule; 5 mg approximately 20 mg lyophilizate; 25 mg approximately 100 mg lyophilizate.

储存及稳定性

Store at -15–-25 °C. (sealed under nitrogen)

分析说明

Specific activity: approximately 750 - 950 U/mg enzyme protein ≅ approximately 150 - 250 U/mg lyophilizate (+37°C, 2-nitrophenyl-β-D-galactoside); approximately 250-400 U/mg enzyme protein ≅ approximately 60-100 U/mg lyophilizate (+37°C, 4-nitrophenyl-β-D-galactoside).

其他说明

仅用于生命科学研究。不可用于诊断。

WGK

WGK 1

闪点(°F)

does not flash

闪点(°C)

does not flash

法规信息

常规特殊物品

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Systemic AAV9 gene transfer in adult GM1 gangliosidosis mice reduces lysosomal storage in CNS and extends lifespan.
Weismann C M, et al.
Human Molecular Genetics, 24(15), 4353-4364 (2015)
Association of the GLB1 rs4678680 genetic variant with risk of HBV-related hepatocellular carcinoma.
Wang W T, et al.
Oncotarget, 7(35), 56501-56501 (2016)
Hideyuki Yaginuma et al.
Lab on a chip, 22(10), 2001-2010 (2022-04-29)
Digital assays using microreactors fabricated on solid substrates are useful for carrying out sensitive assays of infectious diseases and other biological tests. However, sealing of the microchambers using fluid oil is difficult for non-experts, and thus hinders the widespread use
Sasha B Ebrahimi et al.
Nature protocols, 17(2), 327-357 (2022-01-19)
The efficient transfection of functional proteins into cells can serve as a means for regulating cellular processes toward solving fundamental challenges in biology and medicine. However, the use of proteins as effective intracellular agents is hindered by their low cellular
Overflow metabolism in Escherichia coli results from efficient proteome allocation.
Basan M, et al.
Nature, 528(7580), 99-99 (2015)

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