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Purified anti-RNA Polymerase II RPB1 Antibody
产品名称:
Purified anti-RNA Polymerase II RPB1 Antibody
产品类别:
抗体
产品编号:
920203
产品应用:
920203
[价格]
规格 价格 库存
25µg ¥ 1068 1

产品详情

Product Details

Verified Reactivity
Human, Rat
Reported Reactivity
Mouse
Antibody Type
Monoclonal
Host Species
Mouse
Immunogen
The antibody H5 was developed against a purified phosphorylated form of RNA polymerase II extracted from a transformed cell line.
Formulation
Phosphate-buffered solution, pH 7.2, containing 0.09% sodium azide.
Preparation
The antibody was purified by affinity chromatography.
Concentration
0.5 mg/ml
Storage & Handling
The antibody solution should be stored undiluted between 2°C and 8°C.
Application

WB - Quality tested
ICC - Verified
IP - Reported in the literature, not verified in house

Recommended Usage

Each lot of this antibody is quality control tested by Western blotting. For Western blotting, the suggested use of this reagent is 1.0 - 10.0 ?g/ml. For Western blotting, the use of casein or BSA in the blocking solution rather than non-fat-dry milk is recommended. For immunofluorescence microscopy, a concentration range of 1.0 - 5.0 μg/ml is recommended. It is recommended that the reagent be titrated for optimal performance for each application.

Application Notes

Additional reported applications (for the relevant formats) include: immunoprecipitation2,3.

The clone H5 was developed against a purified phosphorylated form of RNA polymerase II extracted from a transformed cell line. Pol II has two physiologically important phosphorylation sites: ser-2 and ser-5. Both sites are found in the heptapeptide repeat YSPTSPS at the C-terminal domain. Clone H5 recognizes the phosphoserine 2 (ser-2) of Pol II. Clone H5 is useful for immunofluorescence and Western blotting.

This clone is not recommended for ChIP (Chromatin Immunoprecipitation) assays (as determined by in-house testing).

This product weakly reacts with Mouse.

Application References

(PubMed link indicates BioLegend citation)
  1. Brown JM, et al. 2008. J. Cell. Biol. 182:1083. (WB, IF)
  2. Bregman DB, et al. 1995. Cell Biol. 129:287-98. (IP)
  3. Ahn SH, et al. 2004. Mol. Cell. 13:67. (IP)
  4. Pellizzoni L, et al. 2001. Cell Biol. 152(1):75. (IF)
  5. Patturajan M, et al. 1998. J. Biol. Chem. 273(8):4689. (WB)
Product Citations
  1. Oqani R, et al. 2016. PLoS One. 11: 0152254. PubMed
  2. Fitzwalter BE, et al. 2018. Dev Cell. 44:555. PubMed
  3. Butler AM, et al. 2018. Development. 145:. PubMed
  4. Wong MM et al. 2018. Developmental cell. 46(3):302-315 . PubMed
  5. Yurko N, et al. 2017. Mol Cell. 68:913. PubMed
  6. Li Y et al. 2017. Development (Cambridge, England). 144(18):3232-3240 . PubMed
  7. Montinaro A, et al. 2021. Cell Death Differ. Online ahead of print. PubMed
  8. Yamashita T, et al. 2017. Sci Rep. 7:39994. PubMed
  9. Ryu HY, et al. 2019. EMBO J. 38:e102003. PubMed
  10. Baluapuri A, et al. 2019. Mol Cell. 74:674. PubMed
  11. Kuhn TM, et al. 2019. J Cell Biol. 218:2945. PubMed
  12. Zhou KI, et al. 2019. Mol Cell. 76:70. PubMed
  13. Tolza C, et al. 2019. Mol Cancer Res. 17:1999. PubMed
  14. Rona G et al. 2018. eLife. 7 pii: e38771. PubMed
  15. Chappidi N, et al. 2020. Molecular Cell. 77(3):528-541.e8.. PubMed
  16. Zhang H et al. 2018. Cell. 175(5):1244-1258 . PubMed
  17. Stanek TJ, et al. 2021. EMBO J. 40:e102509. PubMed
  18. Pancholi A, et al. 2021. Mol Syst Biol. 17:e10272. PubMed
RRID
AB_2734687 (BioLegend Cat. No. 920203) AB_2616695 (BioLegend Cat. No. 920204)

Antigen Details

Structure
RPB1 contains a C-terminus composed of heptapeptide repeats that are essential for polymerase activity. These repeats contain Ser and Thr residues that are phosphorylated in actively transcribing RNA polymerase. The predicted molecular weight is 220 kD.
Distribution

Nucleus and cytosol.

Function
RPB1 is the largest subunit of RNA polymerase II, the polymerase responsible for synthesizing messenger RNA in eukaryotes.
Biology Area
Cell Biology, Cell Cycle/DNA Replication
Gene ID
5430 View all products for this Gene ID
UniProt
View information about RNA Polymerase II on UniProt.org

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