HSF1 ELISA 试剂盒 (Heat Shock Factor Protein 1)

Details for Product HSF1 ELISA Kit No. ABIN2114054, 供应商: Log in to see
抗原
  • hsf1
  • Hsf
  • xhsf1
  • AA960185
  • HSTF1
  • HSF1
  • HSF
  • HSF1c
  • hsf1a
  • hsf1b
  • zHSF1a
  • zHSF1b
  • hstf1
  • heat shock factor
  • Heat Shock Factor
  • heat shock factor 1
  • heat shock transcription factor 1
  • hsf1
  • hsf-1
  • Hsf1
  • HSF1
  • LOC420362
抗原表位
pSer303
适用
人, 小鼠, 大鼠
其他选择
Kits with alternative reactivity to:
21
14
12
2
2
2
2
2
2
1
1
1
实验类型
DNA-Binding ELISA
应用范围
ELISA
选项
Supplier
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Supplier Product No.
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Analytical Method Quantitative
检测方法 Colorimetric
特异性 The HSF1 (Phospho-Ser303) DNA-Binding ELISA Kit detects endogenous levels of HSF1 only when phosphorylated at Ser303.
产品特性 Assay Type: DNA-Binding
别名 HSF1 (HSF1 ELISA Kit 摘要)
背景 Synonyms: Heat shock factor protein 1, Heat shock transcription factor 1, HSF 1, HSTF 1, HSTF1
Gene Symbol: HSF1
基因ID 3297
UniProt Q00613
研究领域 Chromatin and Nuclear Signaling, Transcription Factors, Heat Shock Proteins, Neurology
板类型 Pre-coated
实验流程
  • Remove the coating solution and wash the plate three times by filling the wells with 100 μL PBS-0.05 % Tween20. The solutions or washes are removed by flicking the plate over a sink. The remaining drops are removed by patting the plate on a paper towel.
  • Block the remaining protein-binding sites in the coated wells by adding 100 μL blocking buffer, 3 % skim milk in PBS per well. Incubate for 1 hour at RT with gentle shaking.
  • Wash the plate three times with 100 μL PBS-0.05 % Tween 20.
  • Add 50 μL of diluted antibody to each well. Incubate the plate at 37 °C for an hour with gentle shaking.
  • Wash the plate six times with 100 μL PBS-0.05 %Tween 20.
  • Add 50 μL of conjugated secondary antibody, diluted at the optimal concentration (according to the manufacturer) in blocking buffer immediately before use. Incubate at 37 °C for an hour.
  • Wash the plate six times with 100 μL PBS-0.05 %Tween20.
  • Prepare the substrate solution by mixing acetic acid, TMB and 0.03 % H2O2 with the volume ratio of 4:1:5.
  • Dispense 50 μL of the substrate solution per well with a multichannel pipe. Incubate the plate at 37 °C in dark for 15-30 mins.
  • After sufficient color development, add 100 μL of stop solution to the wells (if necessary).
  • Read the absorbance (optical density at 450nm) of each well with a plate reader.
限制 仅限研究用
注意事项 Avoid multiple freeze-thaw cycles
储存条件 4 °C
储存方法 Store at 4 °C for frequent use, at -20°C for infrequent use.
有效期 6 months
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