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Key Documents

10745731001

Roche

β-Galactosidase

EIA grade

同義詞:

β galactosidase, β-galactosidase

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About This Item

酶委員會編號:
分類程式碼代碼:
12352204

生物源

Escherichia coli

品質等級

化驗

(single peak, HPLC)

形狀

lyophilized

比活性

750-950 U/mg

分子量

540.000  kDa

包裝

pkg of 25 mg (approx. 100 mg lyophilizate)

製造商/商標名

Roche

技術

enzyme immunoassay: suitable

顏色

white

pH值

7.3-7.7

溶解度

water: 20 mg/mL

λmax

405

適合性

suitable for immunoassay

NCBI登錄號

UniProt登錄號

應用

life science and biopharma

運輸包裝

dry ice

儲存溫度

−20°C (−15°C to −25°C)

基因資訊

Escherichia coli ... lacZ(945006)

一般說明

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.

應用

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.

品質

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.

外觀

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.

儲存和穩定性

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

分析報告

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).

其他說明

仅用于生命科学研究。不可用于诊断。

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 1

閃點(°F)

does not flash

閃點(°C)

does not flash


分析證明 (COA)

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存取文件庫

Recurrent and novel GLB1 mutations in India.
Bidchol A M, et al.
Gene, 567(2), 173-181 (2015)
Overflow metabolism in Escherichia coli results from efficient proteome allocation.
Basan M, et al.
Nature, 528(7580), 99-99 (2015)
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
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)

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