ABE1972
Anti-Ash2L Antibody
serum, from rabbit
Sinónimos:
Set1/Ash2 histone methyltransferase complex subunit ASH2, ASH2-like protein
About This Item
Productos recomendados
biological source
rabbit
Quality Level
antibody form
serum
antibody product type
primary antibodies
clone
polyclonal
species reactivity
mouse, human
technique(s)
ChIP: suitable
immunoprecipitation (IP): suitable
western blot: suitable
NCBI accession no.
UniProt accession no.
shipped in
ambient
target post-translational modification
unmodified
Gene Information
human ... ASH2L(9070)
General description
Specificity
Immunogen
Application
Immunoprecipitation Analysis: A representative lot co-immunoprecipitated Mef2 with Ash2L from nuclear extract of differentiating C2C12 murine myoblasts (Rampalli, S., et al. (2007). Nat. Struct. Mol. Biol. 14(12):1150-1156).
Western Blotting Analysis: A representative lot detected full-length as well as N-terminal (a.a. 96 281) and C-terminal (a.a. 317-628) recombinant human Ash2L constructs. Full-length and the C-terminal fragment, but not the N-terminal fragment, were detected in the pull-down by GST-tagged RbBP5 (Avdic, V., et al. (2011). Structure. 19(1):101-108).
Western Blotting Analysis: A representative lot detected Ash2L in Mef2, MLL1, MLL2, MLL3, MLL4, and SET1 immunoprecipitates from differentiating C2C12 murine myoblasts. Ash2L in Mef2 IP was greatly reduced when using lysates from MAP kinase p38 inhibitor-treated cells (Rampalli, S., et al. (2007). Nat. Struct. Mol. Biol. 14(12):1150-1156).
Western Blotting Analysis: A representative lot detected an increased Ash2L pull-down from nuclear extract of differentiating C2C12 murine myoblasts by FLAG-tagged Mef2c and Mef2d following their phosphorylation by p38alpha, while no Ash2L pull-down was seen by Mef2d p38 phosphorylation sites mutatant (Rampalli, S., et al. (2007). Nat. Struct. Mol. Biol. 14(12):1150-1156).
Western Blotting Analysis: A representative lot detected Ash2L in whole cell lysate and nuclear extract, but not cytosolic extract from differentiating C2C12 murine myoblasts, Ash2L shRNA treatment dercreased target band intensity (Rampalli, S., et al. (2007). Nat. Struct. Mol. Biol. 14(12):1150-1156).
Epigenetics & Nuclear Function
Quality
Western Blotting Analysis: A 1:1,000 dilution of this antiserum detected Ash2L in 10 µg of C2C12 murine myoblast lysate.
Target description
Physical form
Storage and Stability
Handling Recommendations: Upon receipt and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance.
Other Notes
Disclaimer
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Storage Class
12 - Non Combustible Liquids
wgk_germany
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
Certificados de análisis (COA)
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