北京木聚糖酶特殊檢測(cè)底物/偶氮木聚糖（樺木）可溶性顯色底物100ml愛爾蘭

木聚糖酶特殊檢測(cè)底物/偶氮木聚糖（樺木）可溶性顯色底物

用于對(duì)- 1 ,4-β-D-木聚糖酶的具體檢測(cè).

外觀：深藍(lán)色粉末或液體

溶解性：易溶于水

pH值：5.5

氣味：無

在室溫下穩(wěn)定，五年或五年以上

成分：

名稱 比例

偶氮木聚糖（樺木）Azo-Xylan （Birchwood） 98％


Azo-Xylan （Birchwood）
Substrate for the specific assay of endo-1,4-ß-D-xylanase.

Catalogue Number: S-AXBL
Content: 100 mL


Appearance Dark blue powder or liquid.
Specific Gravity Not applicable
Solubility in Water Soluble
pH Value ~ 5.5
Odour None
Form Powder
Stability Stable at room temperature for five or more years
Ingredients Name CAS Proportion
Azo-Xylan （Birchwood） 98%


PRINCIPLE:
This assay procedure is specific for endo-1,4-ß-D-xylanase activity.
On incubation of Azo-Xylan （birchwood） with endo-xylanase, the
substrate is depolymerised to produce low-molecular weight dyed
fragments which remain in solution on addition of ethanol to the
reaction mixture. High-molecular weight material is removed by
centrifugation, and the colour of the supernatant is measured. endo-
Xylanase in the sample solution is determined by reference to a
standard curve.
SUBSTRATE:
Birchwood xylan is first purified （to remove starch） and then it is
dyed with Remazolbrilliant Blue R to an extent of approx. one dye
molecule per 30 sugar residues.
DISSOLUTION:
Add 1 g of powdered substrate to 80 mL of boiling and vigorously
stirring water on a hot-plate stirrer. Turn the heat off and continue
stirring until the polysaccharide is compley dissolved （about
20 min）. Adjust the volume to 100 mL and add 0.02 g of sodium
azide and dissolve. Store this solution at 4°C between use. Under
these conditions the solution is stable for 12 months if contamination
with enzyme is avoided. Shake the solution container before
removing aliquots for assays. Because the solution is viscous, it should
preferably be dispensed with a positive displacement dispenser
（eg. Eppendorf Multipette® with a 5.0 mL Combitip）.
PRECIPITANT SOLUTION:
Industrial methylated spirits （IMS; 95 % v/v） or ethanol （95 % v/v）.
BUFFER SOLUTIONS:
1. Sodium acetate buffer, 100 mM, pH 4.5
Add 6.0 g of glacial acetic acid （1.05 g/mL） to 800 mL of distilled
water. Adjust the pH to 4.5 with 5 M （20 g/100 mL） sodium
hydroxide solution. Adjust the volume to 1 litre. Stable for approx.
4 weeks at 4°C.
2. Sodium phosphate buffer, 100 mM, pH 6.0
Add 8.9 g of di-sodium hydrogen phosphate dihydrate
（Na2HPO4•2H2O） to 450 mL of distilled water and dissolve.
Adjust the pH to 6.0 with 1 M hydrochloric. Adjust the volume to
500 mL and add 0.1 g of sodium azide as a preservative. Stable for
approx. 4 weeks at 4°C.
1
ENZYME EXTRACTION AND DILUTION:
Using a positive displacement dispenser, transfer 1.0 mL of liquid
enzyme preparation to 49 mL of buffer 1 （100 mM sodium acetate
buffer, pH 4.5） or buffer 2 （100 mM sodium phosphate buffer, pH 6.0）
and mix thoroughly. This is termed the Original Extract. Dilute
this solution 10-fold by transferring 1.0 mL of diluted enzyme to
9.0 mL of either buffer 1 or buffer 2. Repeat this process until a
dilution of enzyme suitable for assay is obtained.
For powdered enzyme preparations, add 1.0 g of material to 50 mL of
buffer 1 or buffer 2 and gently stir the slurry for 15 min, or until the
sample is compley dispersed or dissolved. Clarify this solution （the
Original Extract） by centrifugation at 1,000 g for 10 min, or by
filtration through Whatman No. 1 （9 cm） filter circles. Dilute this
solution as for the liquid enzyme preparations.
ASSAY PROCEDURE:
Add 0.5 mL of buffered enzyme preparation （pre-equilibrated to
40°C） to 0.5 mL of pre-equilibrated substrate solution （1 % w/v
Azo-Xylan birchwood） with thorough mixing on a vortex stirrer.
Immediay return the mixture to the water bath and incubate at
40°C for exactly 10 min from the time of addition of the enzyme
solution. Terminate the reaction by adding 2.5 mL of ethanol
（95 % v/v） with vigorous stirring on a vortex mixer to the reaction
solution. This will precipitate high-molecular weight, non-hydrolysed
substrate. Store the incubation tubes at room temperature for 5 min
and stir them again. Centrifuge the tubes at 1,000 g （approx. 3,000
rpm for 10 min）. Pour the supernatant solution directly into a
spectrophotometer cuvette and measure the absorbance of the blank
and reaction solutions at 590 nm against water. Determine the
activity by reference to a standard curve. Alternatively, enter the
absorbance values into the appropriate MegaCalcTM available from the
Megazyme website （www.megazyme.com）.
Prepare a reaction blank by adding 2.5 mL of ethanol （or IMS） to
0.5 mL of the substrate solution （1 % w/v） with vigorous stirring.
Immediay add 0.5 mL of the enzyme solution and stir the mixture
vigorously for 10 sec. Because the diluted enzyme preparations are
essentially colourless, a single blank only, is required with each set of
determinations. Typically, blank absorbance values at 590 nm
are ~ 0.07.
2
A standard curve for A. niger endo-b-xylanase （pH optima 4.5） is
shown in Figure 1. Curves for Humicola insolens and Trichoderma
longibrachiatum endo-b-xylanases （pH optima 6.0） are shown in Figures
2 and 3. In each case, the activity of the enzyme preparations
employed were determined using wheat arabinoxylan （Lot 20401）
（10 mg/mL） as substrate, in either 100 mM sodium acetate buffer
（pH 4.5） or sodium phosphate buffer （pH 6.0）. The Nelson-Somogyi
reducing sugar method, with D-xylose as standard, was used to
measure activity.
One unit of enzyme activity is defined as the amount of
enzyme required to release one μmole of D-xylose reducingsugar
equivalents from arabinoxylan, at pH 4.5 （or pH 6.0）
per minute at 40°C.


另有愛爾蘭可溶性呈色底物如下:



Azo-Barley Glucan 100124000 麥芽粉中葡聚糖酶檢測(cè)底物 100 ml S-ABG100 
Azo-Carob Galactomannan 100124001 甘露聚糖酶檢測(cè)底物 4g S-ACGLM 
Azo-Casein （Sulphanilamide Dyed） 100124002 蛋白內(nèi)切酶活性高靈敏度檢測(cè)可溶性底物[相比同類產(chǎn)品其靈敏度高5倍] 10g S-AZCAS 
Azo-CM-Cellulose 100124003 葡聚糖酶檢測(cè)底物 100ml S-ACMCL 
Azo-CM-Cellulose 100124004 葡聚糖酶檢測(cè)底物 4g S-ACMCL 
Azo-Fructan 100124005 內(nèi)切型菊粉酶檢測(cè)底物 5g S-AZFR5 
Azo-Fructan plus exo-Inulinase 100124006 內(nèi)切型菊粉酶特殊檢測(cè)底物 2g+4 KU S-AZFRXOI 
Azo-Galactan（Potato） 100124007 半乳聚糖酶特殊檢測(cè)底物 4g S-AGALP 
Azo-Wheat Arabinoxylan （Azo-Waz） 100124008 木聚糖酶檢測(cè)底物 100ml S-AWAXL 
Azo-Wheat Arabinoxylan （Azo-Waz） 100124009 木聚糖酶檢測(cè)底物 3g S-AWAXP 
Azo-Xylan（Birchwood） 100124010 木聚糖酶特殊檢測(cè)底物 100ml S-AXBL 
Azo-Xylan（Birchwood） 100124011 木聚糖酶特殊檢測(cè)底物 3g S-AXBP 
Azo-Xylan（Oat Spelt） 100124012 木聚糖酶特殊檢測(cè)底物 3g S-AXYO 
Azo-Xyloglucan（Tamarind） 100124013 纖維素酶可溶性發(fā)色檢測(cè)底物 4g S-AZXG 
AZ-Rhamnogalacturonan 100124014 鼠李聚糖半乳糖醛酸內(nèi)切酶檢測(cè)底物 2g S-AZXG 
Red Debranched Arabinan（Sugar Beet） 100124015 阿拉伯聚糖檢測(cè)底物 2g S-AZRH 
Red Pullulan 100124016 酶制備中的普魯蘭酶和麥粉中的極限糊精的檢測(cè)底物 3g S-RDAR 
Red Starch 100124017 Alpha淀粉酶活性檢測(cè)底物 5g S-RPUL

產(chǎn)品關(guān)鍵詞：木聚糖酶特殊檢測(cè)底物/偶氮木聚糖（樺木）可溶性顯色底物