macroH2A.1 Rabbit Polyclonal Antibody
cat.: ER1803-04
Product Type: Rabbit polyclonal IgG, primary antibodies
Species reactivity: Human, Mouse
Applications: WB, IHC-P, FC
Clonality: Polyclonal
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.
Storage buffer: 1*PBS (pH7.4), 0.2% BSA, 50% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1ug/ul
Purification: Immunogen affinity purified.
Molecular weight: Predicted band size: 40 kDa
Isotype: IgG
Immunogen: Recombinant protein within human macroH2A.1 aa 190-369.
Positive control: HeLa cell lysate, MCF7 cell lysate, NIH/3T3 cell lysate, MDA-MB-231 cell lysate, human colon tissue, human placenta tissue, mouse brain tissue, SiHa.
Subcellular location: Nucleus.
Recommended Dilutions:
  WB
  IHC-P
  FC

1:1,000
1:50-1:200
1:50-1:100
Uniprot #: SwissProt: O75367 Human | Q9QZQ8 Mouse
Alternative names: Core histone macro h2a.1 Core histone macro-H2A.1 H2A histone family member Y H2A.y H2A/y H2AF12M H2AFJ H2afy H2AY_HUMAN Histone H2A.Y Histone macroH2A1 Histone macroH2A1.1 Histone macroH2A1.2 Macroh2a1 MACROH2A1.1 MacroH2A1.2 Medulloblastoma antigen MU MB 50.205 Medulloblastoma antigen MU-MB-50.205 mH2a mH2A1
Images
ER1803-04_1.jpg Fig1: Western blot analysis of macroH2A.1 on different lysates with Rabbit anti-macroH2A.1 antibody (ER1803-04) at 1/1,000 dilution.

Lane 1: HeLa cell lysate
Lane 2: MCF7 cell lysate
Lane 3: NIH/3T3 cell lysate
Lane 4: MDA-MB-231 cell lysate

Lysates/proteins at 30 µg/Lane.

Predicted band size: 40 kDa
Observed band size: 40 kDa

Exposure time: 3 minutes;

4-20% SDS-PAGE gel.

Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (ER1803-04) at 1/1,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:100,000 dilution was used for 1 hour at room temperature.
ER1803-04_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded human colon tissue using anti-macroH2A.1 antibody. Counter stained with hematoxylin.
ER1803-04_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded human placenta tissue using anti-macroH2A.1 antibody. Counter stained with hematoxylin.
ER1803-04_4.jpg Fig4: Immunohistochemical analysis of paraffin-embedded mouse brain tissue using anti-macroH2A.1 antibody. Counter stained with hematoxylin.
ER1803-04_5.jpg Fig5: Flow cytometric analysis of SiHa cells with macroH2A.1 antibody at 1/100 dilution (purple) compared with an unlabelled control (cells without incubation with primary antibody; yellow). Alexa Fluor 488-conjugated goat anti-rabbit IgG was used as the secondary antibody.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.