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技術文章

人丙肝(HCV)中英文說明書定性

閱讀:501發(fā)布時間:2011-12-29

人丙肝(HCV)酶聯(lián)免疫分析
試劑盒使用說明書
本試劑盒僅供研究使用。
                                                                                                                                          96T
 
使用目的:
本試劑盒用于測定人血清、血漿及相關液體樣本中丙肝(HCV)表達。
實驗原理
本試劑盒應用雙抗體夾心法測定標本中人丙肝(HCV)表達。用純化的人乙肝(HBV)抗
體包被微孔板,制成固相抗體,可與樣品中丙肝(HCV)相結合,經(jīng)洗滌除去未結合的抗
原和其他成分后再與HRP 標記的丙肝(HCV)抗體結合,形成抗體-抗原-酶標抗體復合物,
經(jīng)過*洗滌后加底物TMB 顯色。TMB 在HRP 酶的催化下轉化成藍色,并在酸的作用下
轉化成zui終的黃色。用酶標儀在450nm波長下測定吸光度 (OD值) ,與 CUTOFF值相比較,
從而判定標本中人丙肝(HCV)的存在與否。
試劑盒組成  
1  30 倍濃縮洗滌液  20ml×1瓶  7  終止液  6ml×1 瓶
2  酶標試劑  6ml×1瓶  8  陽性對照  0.5ml×1 瓶
3  酶標包被板  12 孔×8條  9  陰性對照  0.5ml×1 瓶
4  樣品稀釋液  6ml×1瓶  10  說明書  1 份
5  顯色劑A 液  6ml×1瓶  11  封板膜  2 張    
6  顯色劑B液  6ml×1/瓶  12  密封袋  1 個
標本要求  
1.標本采集后盡早進行提取,提取按相關文獻進行,提取后應盡快進行實驗。若不能
馬上進行試驗,可將標本放于-20℃保存,但應避免反復凍融
2.不能檢測含NaN3的樣品,因NaN3抑制辣根過氧化物酶的(HRP)活性。
操作步驟
1.  編號:將樣品對應微孔按序編號,每板應設陰性對照2 孔、陽性對照2 孔、空白對照1
孔(空白對照孔不加樣品及酶標試劑,其余各步操作相同)
 
 
2.  加樣:分別在陰、陽性對照孔中加入陰性對照、陽性對照 50µl。然后在待測樣品孔先
加樣品稀釋液 40µl,然后再加待測樣品 10µl。加樣將樣品加于酶標板孔底部,盡量不
觸及孔壁,輕輕晃動混勻,
3.  溫育:用封板膜封板后置37℃溫育30分鐘。      
4.  配液:將30 倍濃縮洗滌液用蒸餾水30 倍稀釋后備用
5.  洗滌:小心揭掉封板膜,棄去液體,甩干,每孔加滿洗滌液,靜置 30 秒后棄去,如此
重復 5次,拍干。
6.  加酶:每孔加入酶標試劑50µl,空白孔除外。  
7.  溫育:操作同3。 8.  洗滌:操作同5。
9.  顯色:每孔先加入顯色劑A50µl,再加入顯色劑B50µl,輕輕震蕩混勻,37℃避光顯色
15 分鐘.
10.  終止:每孔加終止液 50µl,終止反應(此時藍色立轉黃色) 。
11.  測定:以空白空調零,450nm波長依序測量各孔的吸光度(OD 值) 。 測定應在加終止
液后 15分鐘以內(nèi)進行。
 
操作程序總結:
 
 
 
 
 
計算和結果判定:
    試驗有效性:陽性對照孔平均值≥1.00; 陰性對照平均值≤0.10
    臨界值(CUT OFF)計算:臨界值=陰性對照孔平均值+0.15
    陰性判定:樣品OD 值< 臨界值(CUT OFF)者為丙肝(HCV)陰性
    陽性判定:樣品OD 值≥  臨界值(CUT OFF)者為丙肝(HCV)陽性
。  
注意事項
1.操作嚴格按照說明書進行,本試劑不同批號組分不得混用。 2.試劑盒從冷藏環(huán)境中取出應在室溫平衡 15-30 分鐘后方可使用,酶標包被板開封后如未
用完,板條應裝入密封袋中保存。
3.濃洗滌液可能會有結晶析出,稀釋時可在水浴中加溫助溶,洗滌時不影響結果。
4. 封板膜只限一次性使用,以避免交叉污染。
5.底物請避光保存。
6.試驗結果判定必須以酶標儀讀數(shù)為準,使用雙波長檢測時,參考波長為630nm
7.所有樣品,洗滌液和各種廢棄物都應按傳染物處理。終止液為 2M 的硫酸,使用時必須
注意安全。
保存條件及有效期
1.試劑盒保存: ;2-8℃。
2.有效期:6個月
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 Human HCV
FOR RESEARCH USE ONLY
 
                                                                                                  96 determinations
Purpose
This  kit  allows  for  the  determination  of  HCV  expression  in  Human  serum,  and  other
biological fluids.
Principle of the assay
The kit assay HCV level in the sample, use Purified HCV antibody to coat microtiter plate
wells, make solid-phase antibody, then add HCV to wells, Combined With HCV, after washing
and removing non-combinative antibody and other components ,then Combined HCV antibody  
which with HRP labeled become antibody – antigen - enzyme- antibody complex, after washing
Compley,  Add  TMB  substrate  solution,,  TMB  substrate  becomes  blue  color  At  HRP
enzyme-catalyzed,  reaction  is  terminated by  the addition of a sulphuric acid  solution and  the
color change  is measured spectrophotometrically at a wavelength of 450 nm. Compared with
the CUTOFF value, according to this to judge HCV exist in the sample or not.
Materials provided with the kit
1  wash    solution  20ml×1bottle  7  Stopp Solution  6ml×1 bottle
2  HRP-Conjugate reagent  6ml×1 bottle  8  Positive control  0.5ml×1 bottle
3  Microelisa stripplate  12well×8strips  9  Negative control  0.5ml×1bottle
4  Sample diluent  6ml×1 bottle  10  Instruction  1
5  Chromogen Solution A  6ml×1 bottle  11
Closure plate
membrane
2
6  Chromogen Solution B  6ml×1 bottle  12  Sealed bags  1
 
Specimen requirements
1.  extract  as  soon  as  possible  after  Specimen  collection,and  according  to  the  relevant
literature,  and  should  be  experiment  as  soon  as  possible  after  the  extraction.  If  it  can’t,
specimen can be kept in -20 ℃ to preserve, Avoid repeated freeze-thaw cycles. 2.  Can’t detect the sample which contain NaN3, because NaN3 inhibits HRP active.
Assay procedure
1.Number: to sample correspond microtitration well and Number Sequence, each plate should
be  set  feminine  comparison  2  wells,  masculine  comparison  2  wells,  blank  comparison  1
well(don’t add sample and HRP-Conjugate reagent to blank comparison well, other each step
the operation are same).
2.add sample:separay add Positive control and Negative control 50µl  to  the Positive and
Negative well . add Sample dilution 40µl to testing sample well, then add testing sample 10µl.
add  sample  to  the bottom of ELISA plates  coated well  , don’t  touch  the well wall as  far as
possible, and Gently mix.
3.Incubate: After closing plate with Closure plate membrane ,incubate for 30 min at 37℃.    
4.Configurate  liquid: 30-fold  (or 20-fold)wash solution diluted 30-fold  (or 20-fold) with distilled
water until 600ml,and reserve.
5.washing:Uncover Closure plate membrane, discard Liquid, dry by swing, add washing buffer
to every well, still for 30s then drain, repeat 5 times, dry by pat.
6.add enzyme:Add HRP-Conjugate reagent 50µlto each well, except the blank well.  
7.incubate:Operation with 3.
8.washing:Operation with 5.
9.color:Add Chromogen Solution A 50ul and Chromogen Solution B  to each well, evade  the
light preservation for 15 min at 37℃
10.Stop  the  reaction:Add  Stop  Solution50µl  to  each well,  Stop  the  reaction(the  blue  color
change to yellow color).
11. assay: take blank well as zero , Read absorbance at 450nm after Adding Stop Solution and
within 15min.
Determine the result Test validity: the average of Positive control well≥1.00; the average of Negative control well
≤0.10.
Calculate Critical(CUT OFF) : Critical= the average of Negative control well + 0.15.
Negative control: sample OD< Calculate Critical(CUT OFF) is HCV Negative control.
Positive control: ample OD≥ Calculate Critical(CUT OFF) is HCV Positive control.
Important notes
1.Please according to use instruction strictly, Do not mix reagents with those from other lots.
2.The kit  takes out  from  the  refrigeration environment should be balanced 15-30 minutes  in
the  room  temperature    then use, ELISA plates coated  if has not use up after opened,  the
plate should be stored in Sealed bag.
3.washing  buffer  will  Crystallization  separation,  it  can  be  heated  the  water  helps  dissolve
when dilute . Washing does not affect the result.
4.Closure plate membrane only  limits  the disposable use,  in order  to avoid  the overlapping
pollution
5.The substrate please evade the light preservation.
6.The test result determination must take the microtiter plate reader as a standard, when use
dual-wavelength to assay, Reference wavelength is 630nm.
7.All samples, washing buffer and each kind of  reject should according  to  infective material
process. Stopp Solution is 2M sulphuric acid. You must pay attention to safe when use .
Storage and validity
1.Storage:    2-8℃.
2.validity:  six months. 
 


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