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In Situ Cell Death Detection Kit, AP 細胞凋亡檢測試劑盒(AP )

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產品名稱: In Situ Cell Death Detection Kit, AP 細胞凋亡檢測試劑盒(AP )
產品型號: Roche 11684809910
產品展商: 其他品牌
產品文檔: 無相關文檔

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In Situ Cell Death Detection Kit, AP 細胞凋亡檢測試劑盒(AP )


In Situ Cell Death Detection Kit, AP 細胞凋亡檢測試劑盒(AP )  的詳細介紹
In Situ Cell Death Detection Kit, AP 細胞凋亡檢測試劑盒(AP )

細胞凋亡檢測試劑盒(AP )

 

羅氏細胞檢測系列產品自問世以來,歷經時間的考驗,以其**的品質獲得了廣大業界用戶的支持和認可,相關文獻達數千篇。
細胞凋亡產品特性:
檢測范圍廣泛:可實現對細胞培養液、組織切片、單個細胞及細胞群落的分析檢測,滿足日益增長的高通量檢測需求。
檢測方法靈活:針對光學或熒光顯微鏡、流式細胞儀、ELISA
操作**:無需接觸任何放射性同位素,簡便易用。
產品線豐富:針對不同的細胞凋亡通路,有多種產品可供挑選。
一、檢測Caspase活性
  caspase對角蛋白18的裂解作用
   產品名及貨號:M30 CytoDEATH 12140349001
          M30 CytoDEATH,Fluorescein 12156857001
       Caspase-3活性
          產品名及貨號:Caspase 3 Activity Assay 12012952001
       Caspase
          產品名及貨號:Homogeneous Caspase Assay,fluorimetric 03005372001
       CaspaseRARP的裂解作用
   產品名及貨號:Anti-Poly(ADP-Ribose)Polymerase(PARP) 11835238001
二、檢測DNA片斷
  TUNEL檢測法
   產品名及貨號:In Situ Cell Death Detection Kit,AP 11684809910
                            In Situ Cell Death Detection Kit,POD 11684817910
                            In Situ Cell Death Detection Kit,Fluorescein 11684795910
                            In Situ Cell Death Detection Kit,TMR red 12156792910
  Elisa檢測
   產品名及貨號:Cell Death Detection Elisa 11774425001
      凝膠電泳檢測
   產品名及貨號:Apoptotic DNA Ladder Kit 11835246001
三、檢測膜變化
  產品名及貨號:Annexin-V-FLUOS 11828681001
                       Annexin-V-FLUOS Staining Kit 11988549001
                       Annexin-V-Alexa 568 03703126001
                       Annexin-V-Biotin 11828690001
四、檢測DNA合成
  BrdU標記檢測
  產品名及貨號:Celluar DNA Fragmentation  ELISA  11585045001

ROCHE相關產品資料

In Situ Cell Death Detection Kit, AP

Kit for the detection and quantification of apoptotic cell death on a single-cell level by light microscopy in immunohistocytochemistry.

Catalog : 11684809910

Pack size :1 kit for up to 50 tests

Application

Qualitative detection of apoptosis at the single-cell level by light microscopy.

Benefits

  • Sensitive: The maximum intensity of labeling (cell staining) of apoptotic cells is higher than the nick translation method
  • Fast: The use of fluorescein-dUTP allows analysis of the samples directly after the TUNEL reaction, but before the addition of the secondary detection system
  • Convenient: The direct labeling procedure using fluorescein-dUTP allows verification of the efficiency of the TUNEL reaction during the assay procedure
  • Accurate: Identification of apoptosis at a molecular level (DNA-strand breaks) and identification of cells at the very early stages of apoptosis
  • Flexible: No substrate included; provides the opportunity to select the staining procedure of choice

Product Description

Sample material: Cytospin and cell smear preparations, adherent cells grown on slides, and frozen and paraffin-embedded tissue sections.

Background Information

Widely used methods to determine apoptosis include the analysis of the genomic DNA by agarose-gel electrophoresis and DNA fragmentation assays based on 3H-thymidine and, alternatively, 5-Bromo-2'-deoxy-uridine. The methods involve the separation of fragmented, low molecular-weight DNA from unfragmented, high molecular-weight DNA in a given cell population. Thus, these methods do not provide information about the fate of an individual cell in a given cell population or, particularly, in tissue sections. Alternatively, individual apoptotic cells may be microscopically recognized because of the characteristic appearance of nuclear chromatin condensation and fragmentation, but this method is subjective and limited to a relatively narrow time window when the morphological changes are at a maximum.
The hallmark of apoptosis is DNA degradation, which in early stages is selective to the internucleosomal DNA linker regions. The DNA cleavage may yield double-stranded and single-stranded DNA breaks (nicks). Both types of breaks can be detected by labeling the free 3'-OH termini with modified nucleotides (e.g., biotin-dUTP, DIG-dUTP, fluorescein-dUTP) in an enzymatic reaction. The enzyme terminal deoxynucleotidyl transferase (TdT) catalyzes the template-independent polymerization of deoxyribonucleotides to the 3'-end of single- and double-stranded DNA. This method has also been termed TUNEL (TdT-mediated dUTP-X nick end labeling). Alternatively, free 3'-OH groups may be labeled using DNA polymerases by the template-dependent mechanism called nick translation. However, the TUNEL method is considered to be more sensitive and faster.

Contents

  1. Enzyme Solution (TdT), 5 vials
  2. Label Solution (fluorescein-dUTP), 5 vials
  3. Converter AP (anti-fluorescein antibody-AP), ready-to-use
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