跳轉至內容
Merck

跳轉至

WTA2

TransPlex® Complete Whole Transcriptom Amplification Kit

DNA polymerase included, Complete Kit with optimized enzyme to amplify total RNA in <4 hours, no 3′ bias

同義詞:

完整全转录组扩增试剂盒

檢視組織與合約價格。

選擇尺寸

變更視圖
給您/庫存單位供貨能力價格

關於此項目

NACRES:
NA.55
UNSPSC Code:
41121800
暫時無法取得訂價和供貨情況
技術服務
需要援助?我們經驗豐富的科學家團隊隨時樂意為您提供支援。
讓我們為您提供幫助


Quality Segment

technique(s)

whole genome amplification: suitable

dilution

(WTA)

input

purified RNA

shipped in

wet ice

storage temp.

−20°C

General description

经过优化的WTA2,可对福尔马林固定的石蜡包埋样品(FFPE)和其他受损或降解样本中的RNA进行扩增。全转录组扩增(WTA)技术可在4小时内对ng级的总RNA进行无3′偏差的代表性扩增。扩增产物适用于qPCR、微阵列分析和克隆等应用。WTA2试剂盒含有cDNA文库扩增所需的聚合酶。

Application

适于各种下游应用,包括:
  • qPCR
  • 微阵列分析
  • 克隆
完整全转录组扩增试剂盒用于:
  • 建立过程控制深度测序同时分析猪粪便中DNA和RNA病毒的实验方案。[1]
  • 反转录和cDNA扩增[2][3][4]
  • 使用免疫捕获PPV颗粒释放的基因组RNA来合成和扩增cDNA库[5]
  • 核酸制备和深度测序(提取的核酸随机引物用于cDNA合成)[6]

Biochem/physiol Actions

WTA2过程包括2个步骤。第一步,使用由拟随机3′端和通用5′端组成的非自身互补引物对样品RNA进行逆转录。在该过程中,被取代的单链将作为引物退火和延伸的新模板。所得OmniPlex cDNA文库由以通用末端序列为侧翼序列、含100-1000个碱基的随机重叠片段组成。第二步,使用WTA2聚合酶和通用末端引物对cDNA文库进行PCR扩增,生成WTA2产物。

Features and Benefits

  • 在4小时内实现高达10,000x的扩增,并且手动操作时间低于30分钟
  • 仅需20 pg的总RNA模板,即可扩增出适用于微阵列分析的cDNA
  • 含有cDNA扩增所需的所有元件
  • 实现对表达基因和外显子的线性扩增,无3′或5′偏差
  • 有效扩增单细胞或小量RNA,包括来自动物、植物或微生物的mRNA和总RNA。

比較類似項目

查看完整比較

Show Differences

1 of 1

本產品
WGA2SEQRWTA1
technique(s)

whole genome amplification: suitable

technique(s)

whole genome amplification: suitable

technique(s)

whole genome amplification: suitable

technique(s)

whole genome amplification: suitable

shipped in

wet ice

shipped in

wet ice

shipped in

wet ice

shipped in

wet ice

dilution

(WTA)

dilution

(WGA)

dilution

(WTA)

dilution

(WTA)

input

purified RNA

input

purified DNA

input

purified RNA

input

purified DNA

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200


套裝中的組件也可單獨購買

產品號碼
描述
SDS & 訂價

  • Library Synthesis Enzyme
    SDS

  • Library Synthesis Solution
    SDS

  • Amplification Mix
    SDS

  • Library Synthesis Buffer
    SDS

  • Water, Nuclease-Free Water, for Molecular Biology
    SDS

  • Amplification Enzyme
    SDS

  • Deoxynucleotide Mix, 10 mM, Molecular Biology Reagent
    SDS

存儲類別/等級

10 - Combustible liquids

wgk

WGK 3



從最近期的版本中選擇一個:

分析證明 (COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our 文件 section.

如果您需要協助,請聯絡 客戶支援

已經擁有該產品?

您可以在文件庫中找到最近購買的產品相關文件。

存取文件庫



Questions

  1. What are the differences between WTA1 and WTA2?

    1 answer
    1. WTA2 is designed to amplify RNA from formalin-fixed, paraffin-embedded (FFPE) and other damaged or degraded samples. Here are the main differences between the two kits:

      1. WTA1 was developed by Rubicon. WTA2 was developed by Sigma-Aldrich.
      2. The library synthesis primers for WTA2 are different and can prime more frequently, which is crucial for degraded RNAs.
      3. The library synthesis conditions are different due to the change in the primers.
      4. There are improved cycling conditions in WTA2 to optimize amplification of both high AT templates and high GC templates.
      5. WTA1 does not contain an amplification enzyme, which needs to be supplied separately. WTA2 includes the amplification enzyme.

      Helpful?

Reviews

No rating value

Active Filters