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Goat Anti-Rabbit IgG (H+L), F(ab')2 Fragment (Alexa Fluor® 647 Conjugate)

Goat Anti-Rabbit IgG (H+L), F(ab')2 Fragment (Alexa Fluor® 647 Conjugate)

货号: S0B4041
价格: 1856
规格: 1mg
介绍: -
其他: -
产品规格
  • 宿主来源

    Goat
  • 抗原名称

    Rabbit IgG
  • 免疫原

    Rabbit IgG
  • 抗体类型

    Polyclonal antibody
  • 应用

    IF
  • 反应种属 ?

    Rb
  • 纯化方式

    Immunogen Affinity
  • 浓度

    2 mg/ml
  • 标记

    Alexa Fluor® 647
  • 性状

    Liquid
  • 缓冲体系

    PBS, 25% Glycerol, 1% BSA, 0.3% Proclin 300
  • 储存条件

    12 months from date of receipt / reconstitution, -20 °C as supplied

稀释度
应用 稀释度 推荐种属
IF 1:500 Rb
背景介绍
  • Goat Anti-Rabbit IgG (H+L), F(ab')2 Fragment is a type of secondary antibody fragment that is widely utilized in various immunological assays due to its specific characteristics. Derived from immunoglobulins of goats that have been immunized against rabbit IgG, this fragment consists of the antigen-binding regions (Fab')2 of the antibody molecule, which includes both the heavy (H) and light (L) chains. The F(ab')2 fragment is obtained by enzymatic digestion of the whole IgG molecule, specifically using pepsin, which cleaves the molecule into pieces while retaining the antigen-binding sites.

  • 免疫荧光

    • IF shows positive staining in paraffin-embedded human tonsil. Anti-Claudin 3+Claudin 9 antibody (S0B2348) was used at 1/200 dilution (magenta) and incubated overnight at 4°C. Goat Anti-Rabbit IgG (H+L), F(ab')2 Fragment (Alexa Fluor® 647 Conjugate) was used as secondary antibody at 1/500 dilution. Counterstained with DAPI (Blue). Heat mediated antigen retrieval with EDTA buffer pH9.0 was performed before commencing with IF staining protocol.

    • IF shows positive staining in paraffin-embedded human stomach. Anti- Claudin 3+Claudin 9 antibody (S0B2348) was used at 1/200 dilution (magenta) and incubated overnight at 4°C. Goat Anti-Rabbit IgG (H+L), F(ab')2 Fragment (Alexa Fluor® 647 Conjugate) was used as secondary antibody at 1/500 dilution. Counterstained with DAPI (Blue). Heat mediated antigen retrieval with EDTA buffer pH9.0 was performed before commencing with IF staining protocol.