Anti-Histone H1 (tri methyl K25) antibody (ab17347)
Key features and details
- Rabbit polyclonal to Histone H1 (tri methyl K25)
- Suitable for: WB, ICC/IF
- Reacts with: Human
- Isotype: IgG
Overview
-
Product name
Anti-Histone H1 (tri methyl K25) antibody -
Description
Rabbit polyclonal to Histone H1 (tri methyl K25) -
Host species
Rabbit -
Specificity
ab17347 gives a positive result against the immunizing peptide and a negative result against the corresponding unmodified peptide in ELISA analysis. ab17347 recognises histone H1 tri methyl K25 in HeLa nuclear and whole cell lysates at 35 kDa. The signal is efficiently blocked using the immunzing histone H1 tri methyl K25 peptide but not the corrseponding unmodified peptide or histone H1 di methyl K25 peptide. ab17347 also appears to recognise other bands between 34 kDa and 37 kDa, which are attributed to the antibody recognising other isoforms of histone H1. ab17347 also appears to recognise methylated histone H3 at 17 kDa. -
Tested Applications & Species
See all applications and species dataApplication Species ICC/IF HumanWB Human -
Immunogen
Synthetic peptide corresponding to Human Histone H1 aa 1-100 (internal sequence) conjugated to keyhole limpet haemocyanin.
(Peptide available asab17587) -
General notes
HeLa nuclear lysate
Properties
-
Form
Liquid -
Storage instructions
Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle. -
Storage buffer
pH: 7.40
Preservative: 0.02% Sodium azide
Constituent: PBS
Batches of this product that have a concentrationConcentration information loading...Purity
Immunogen affinity purifiedClonality
PolyclonalIsotype
IgGResearch areas
Associated products
-
Compatible Secondaries
-
Control Peptide
-
Isotype control
-
Recombinant Protein
Applications
The Abpromise guarantee
Our Abpromise guarantee covers the use of ab17347 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
GuaranteedTested applications are guaranteed to work and covered by our Abpromise guarantee.
PredictedPredicted to work for this combination of applications and species but not guaranteed.
IncompatibleDoes not work for this combination of applications and species.
Application Species ICC/IF HumanWB HumanAll applications CowNon human primatesApplication Abreviews Notes WB (1) Use a concentration of 1 µg/ml. Detects a band of approximately 35 kDa (predicted molecular weight: 35 kDa).ICC/IF (1) Use a concentration of 1 µg/ml.Notes WB
Use a concentration of 1 µg/ml. Detects a band of approximately 35 kDa (predicted molecular weight: 35 kDa).ICC/IF
Use a concentration of 1 µg/ml.Target
-
Relevance
Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. Linker histones are involved in the formation of higher order structure in chromatin and the maintenance of overall chromatin compaction. Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fibre is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. Methylation of position-specific lysine residues in histone N termini is a central modification for regulating epigenetic transitions in chromatin. Each methylatable lysine residue can exist in a mono-, di-, or trimethylated state. Arginine resdiues can also by mono or di methylated. -
Cellular localization
Nuclear -
Database links
- Entrez Gene: 3005 Human
- Omim: 142708 Human
- SwissProt: P10412 Human
- Unigene: 226117 Human
-
Alternative names
- H1 antibody
- H1.4 antibody
- histone H1.4 antibody
Images
-
All lanes : Anti-Histone H1 (tri methyl K25) antibody (ab17347) at 1 µg/ml
Lane 1 : HeLa nuclear lysate
Lane 2 : HeLa whole cell lysate
Lane 3 : HeLa nuclear lysate with Human Histone H1 (tri methyl K25) peptide (ab17587) at 1 µg/ml
Lane 4 : HeLa whole cell lysate with Human Histone H1 (tri methyl K25) peptide (ab17587) at 1 µg/ml
Lane 5 : HeLa nuclear lysate withHuman Histone H1 peptide (ab17588) at 1 µg/ml
Lane 6 : HeLa whole cell lysate withHuman Histone H1 peptide (ab17588) at 1 µg/ml
Lane 7 : HeLa nuclear lysate with Human Histone H1 (di methyl K25) peptide (ab21998) at 1 µg/ml
Lane 8 : HeLa whole cell lysate with Human Histone H1 (di methyl K25) peptide (ab21998) at 1 µg/ml
Lysates/proteins at 20 µg per lane.
Secondary
All lanes : Goat polyclonal to Rabbit IgG (Alexa Fluor® 680) at 1/10000 dilution at 1/10000 dilution
Predicted band size: 35 kDa
Observed band size: 35 kDa
Additional bands at: 17 kDa (possible cross reactivity)
ab17347 recognises histone H1 tri methyl K25 in HeLa nuclear (lane1) and whole cell (lane2) lysates at 35 kDa. The signal is efficiently blocked using the immunizing histone H1 tri methyl K25 peptide (lanes3-4) but not the corrseponding unmodified peptide (lanes5-6) or histone H1 di methyl K25 peptide (lanes7-8).
ab17347 also appears to recognise other bands between 34 kDa and 37 kDa, which are attributed to the antibody recognising other isoforms of histone H1.
The strong signal at 17 kDa is attributed methylated histone H3. -
ICC/IF image of ab17347 stained human HepG2 cells. The cells were methanol fixed (5 min), permabilised in 0.1% PBS-Tween (20 min) and incubated with the antibody (ab17347, 1µg/ml) for 1h at room temperature. 1%BSA / 10% normal goat serum / 0.3M glycine was used to block non-specific protein-protein interactions. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red). DAPI was used to stain the cell nuclei (blue). This antibody also gave a positive IF result in HeLa, HEK 293, MCF7 cells.
Protocols
Datasheets and documents
References (1)
ab17347 has been referenced in 1 publication.
- Agger K et al. UTX and JMJD3 are histone H3K27 demethylases involved in HOX gene regulation and development. Nature 449:731-4 (2007). ICC/IF ; Human . PubMed: 17713478
Images
-
All lanes : Anti-Histone H1 (tri methyl K25) antibody (ab17347) at 1 µg/ml
Lane 1 : HeLa nuclear lysate
Lane 2 : HeLa whole cell lysate
Lane 3 : HeLa nuclear lysate with Human Histone H1 (tri methyl K25) peptide (ab17587) at 1 µg/ml
Lane 4 : HeLa whole cell lysate with Human Histone H1 (tri methyl K25) peptide (ab17587) at 1 µg/ml
Lane 5 : HeLa nuclear lysate withHuman Histone H1 peptide (ab17588) at 1 µg/ml
Lane 6 : HeLa whole cell lysate withHuman Histone H1 peptide (ab17588) at 1 µg/ml
Lane 7 : HeLa nuclear lysate with Human Histone H1 (di methyl K25) peptide (ab21998) at 1 µg/ml
Lane 8 : HeLa whole cell lysate with Human Histone H1 (di methyl K25) peptide (ab21998) at 1 µg/ml
Lysates/proteins at 20 µg per lane.
Secondary
All lanes : Goat polyclonal to Rabbit IgG (Alexa Fluor® 680) at 1/10000 dilution at 1/10000 dilution
Predicted band size: 35 kDa
Observed band size: 35 kDa
Additional bands at: 17 kDa (possible cross reactivity)
ab17347 recognises histone H1 tri methyl K25 in HeLa nuclear (lane1) and whole cell (lane2) lysates at 35 kDa. The signal is efficiently blocked using the immunizing histone H1 tri methyl K25 peptide (lanes3-4) but not the corrseponding unmodified peptide (lanes5-6) or histone H1 di methyl K25 peptide (lanes7-8).
ab17347 also appears to recognise other bands between 34 kDa and 37 kDa, which are attributed to the antibody recognising other isoforms of histone H1.
The strong signal at 17 kDa is attributed methylated histone H3. -
ICC/IF image of ab17347 stained human HepG2 cells. The cells were methanol fixed (5 min), permabilised in 0.1% PBS-Tween (20 min) and incubated with the antibody (ab17347, 1µg/ml) for 1h at room temperature. 1%BSA / 10% normal goat serum / 0.3M glycine was used to block non-specific protein-protein interactions. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red). DAPI was used to stain the cell nuclei (blue). This antibody also gave a positive IF result in HeLa, HEK 293, MCF7 cells.