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Read our guarantee »Products:Epigenetics and Nuclear Signaling >> Histones >> Variants
Anti-Histone H2A.Z (acetyl K4 + K7 + K11) antibody - ChIP Grade
See all Histone H2A.Z products (8) ...
Sheep polyclonal to Histone H2A.Z (acetyl K4 + K7 + K11) - ChIP Grade
ChIP, IF, WBmore details
Reacts with
Mouse, Chicken, Human
Synthetic peptide conjugated to KLH derived from within residues 1 - 100 of Chicken H2A.Z.
AGGKAcAGKA cDSGKAcAKA KAC
Liquid
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
Preservative: 0.02% Sodium Azide
Constituents: 1% BSA, PBS
Concentration information loading...
Immunogen affinity purified
Polyclonal
IgG
Our Abpromise guarantee covers the use of ab18262 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
ChIP: Use at an assay dependent dilution.
IF: Use at an assay dependent dilution.
WB: Use at an assay dependent dilution. Detects a band of approximately 14 kDa (predicted molecular weight: 13 kDa).
The conserved histone variant H2A.Z functions in euchromatin to antagonize the spread of heterochromatin. The mechanism by which histone H2A is replaced by H2A.Z in the nucleosome is unknown. However, the recently isolated SWR1 complex catalyzes an ATP-dependent histone exchange with specificity for the histone variant H2A.Z. This provides a new theme in chromatin remodeling mechanisms and an explanation of how histone variants are incorporated into the nucleosome outside of S phase. In connection with the isolation of histone variant specific chaperone complexes, we are beginning to see the mechanisms that mix the histone octamer with intriguing implications for epigenetic inheritance. During early mammalian development H2A.Z plays an essential, but unknown, function(s). It has been shown (Rangasamy et al., 2003) that undifferentiated mouse cells of the inner cell mass lack H2A.Z, but upon differentiation H2A.Z expression is switched on. Strikingly, H2A.Z is first targeted to pericentric hetero chromatin and then to other regions of the nucleus, but is excluded from the inactive X chromosome and the nucleolus.
Nuclear
Western blot - H2A.Z (acetyl K4 + K7 + K11) antibody - ChIP Grade (ab18262)

All lanes : Anti-Histone H2A.Z (acetyl K4 + K7 + K11) antibody - ChIP Grade (ab18262)
Lane 1 : Butyrate-treated HeLa histones
Lane 2 : 15-day embryo chicken erythrocyte histones
Lane 3 : Recombinant H2A.Z
Lane 4 : Butyrate-treated HeLa histones
Lane 5 : 15-day embryo chicken erythrocyte histones
Lane 6 : Recombinant H2A.Z
Predicted band size : 13 kDa
Observed band size : 13 kDa
Prof Colyn Crane-Robinson
Western blot - H2A.Z (acetyl K4 + K7 + K11) antibody - ChIP Grade (ab18262)

All lanes : Anti-Histone H2A.Z (acetyl K4 + K7 + K11) antibody - ChIP Grade (ab18262)
Lane 1 : Butyrate-treated HeLa histones
Lane 2 : Nucleosomes from 10-day chicken brain tissue. ChIP Input.
Lane 3 : Nucleosomes from 10-day chicken brain tissue. ChIP Unbound.
Lane 4 : Nucleosomes from 10-day chicken brain tissue. ChIP Bound.
Lane 5 : Butyrate-treated HeLa histones
Lane 6 : Nucleosomes from 10-day chicken brain tissue. ChIP Input.
Lane 7 : Nucleosomes from 10-day chicken brain tissue. ChIP Unbound.
Lane 8 : Nucleosomes from 10-day chicken brain tissue. ChIP Bound.
Predicted band size : 13 kDa
Observed band size : 13 kDa
Nucleosomes from 10-day chicken brain tissue were used in ChIP experiments. An acetic acid / urea / Triton gel was run and the corresponding western blot using ab18262 was used to compare proteins in the Bound chromatin fraction with those of the Input and Unbound fractions. In lane 8 there is a strong diffuse band corresponding to a hyper-acetylated H2A.Z.
Prof Colyn Crane-Robinson
This product has been referenced in:
See all 5 publications for this product
Publishing research using ab18262? Please let us know so that we can cite the reference in this datasheet
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All lanes : Anti-Histone H2A.Z (acetyl K4 + K7 + K11) antibody - ChIP Grade (ab18262)
Lane 1 : Butyrate-treated HeLa histones
Lane 2 : 15-day embryo chicken erythrocyte histones
Lane 3 : Recombinant H2A.Z
Lane 4 : Butyrate-treated HeLa histones
Lane 5 : 15-day embryo chicken erythrocyte histones
Lane 6 : Recombinant H2A.Z
Predicted band size : 13 kDa
Observed band size : 13 kDa
Prof Colyn Crane-Robinson

All lanes : Anti-Histone H2A.Z (acetyl K4 + K7 + K11) antibody - ChIP Grade (ab18262)
Lane 1 : Butyrate-treated HeLa histones
Lane 2 : Nucleosomes from 10-day chicken brain tissue. ChIP Input.
Lane 3 : Nucleosomes from 10-day chicken brain tissue. ChIP Unbound.
Lane 4 : Nucleosomes from 10-day chicken brain tissue. ChIP Bound.
Lane 5 : Butyrate-treated HeLa histones
Lane 6 : Nucleosomes from 10-day chicken brain tissue. ChIP Input.
Lane 7 : Nucleosomes from 10-day chicken brain tissue. ChIP Unbound.
Lane 8 : Nucleosomes from 10-day chicken brain tissue. ChIP Bound.
Predicted band size : 13 kDa
Observed band size : 13 kDa
Nucleosomes from 10-day chicken brain tissue were used in ChIP experiments. An acetic acid / urea / Triton gel was run and the corresponding western blot using ab18262 was used to compare proteins in the Bound chromatin fraction with those of the Input and Unbound fractions. In lane 8 there is a strong diffuse band corresponding to a hyper-acetylated H2A.Z.
Prof Colyn Crane-Robinson
1
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