Antibody data
- Antibody Data
- Antigen structure
- References [0]
- Comments [0]
- Validations
- Western blot [1]
- Immunocytochemistry [2]
- Other assay [1]
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Validation data
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- Product number
- PA5-112465 - Provider product page
- Provider
- Invitrogen Antibodies
- Product name
- Acetyl-Histone Macro-H2A.1 (Lys13) Polyclonal Antibody
- Antibody type
- Polyclonal
- Antigen
- Synthetic peptide
- Reactivity
- Human
- Host
- Rabbit
- Isotype
- IgG
- Vial size
- 100 µL
- Concentration
- 0.12 mg/mL
- Storage
- -20°C or -80°C if preferred
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Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Western Blot analysis of Acetyl Histone Macro-H2A.1 (Lys13) in multiple sample types using a Acetyl Histone Macro-H2A.1 (Lys13) polyclonal antibody (Product # PA5-112465) at a concentration of 1.25 µg/ml. A goat anti rabbit polyclonal secondary antibody was used at a dilution of 1:50,000. Sample types that were tested include: Hela whole cell lysate, 293 whole cell lysate, A549 whole cell lysate, Jurkat whole cell lysate, HepG2 whole cell lysate (all treated with 30mM sodium butyrate for 4h) .
Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Immunocytochemichal analysis of Acetyl Histone Macro-H2A.1 (Lys13) in Hela cells using a Polyclonal antibody (Product # PA5-112465) at a dilution of 1:5. Hela cells (treated with 30mM sodium butyrate for 4 hour) performed on a Leica BondTM system. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Immunocytochemichal analysis of Acetyl Histone Macro-H2A.1 (Lys13) in Hela cells using a Polyclonal antibody (Product # PA5-112465) at a dilution of 1:2.5. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4°C. The secondary antibody was Alexa Fluor 488-congugated Goat Anti-Rabbit IgG(H+L). Cells were also counter-stained with DAPI.
Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Immunoprecipitation analysis of Acetyl Histone Macro-H2A.1 (Lys13) in 293 whole cell lysate using a Polyclonal antibody (Product #PA5-112465). An HRP-conjugated Protein G antibody was used as the secondary antibody (1:2,000). Lane 1: Rabbit control IgG, Lane 2: 5 µg primary antibody and 500 µg of 293 whole cell lysate, Lane 3:20 µg of 293 whole cell lysate.