HLA Class II DRB1 Recombinant Rabbit Monoclonal Antibody [JE60-43]
cat.: HA721927
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human
Applications: WB, IHC-P, IF-Tissue
Clonality: Monoclonal
Clone number: JE60-43
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.
Storage buffer: 1*TBS (pH7.4), 0.05% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1ug/ul
Purification: Protein A affinity purified.
Molecular weight: Predicted band size: 30 kDa
Isotype: IgG
Immunogen: Synthetic peptide within Human HLA Class II DRB1 aa 151-200 / 266.
Positive control: Ramos cell lysate, Raji cell lysate, Daudi cell lysate, HDLM-2 cell lysate, A375 cell lysate, human tonsil tissue, human skin tissue, human diffuse large B-cell lymphoma tissue.
Subcellular location: Cell membrane. Endoplasmic reticulum.
Recommended Dilutions:
  WB
  IHC-P
  IF-Tissue

1:1,000
1:1,000
1:100
Uniprot #: SwissProt: P01911 Human | P01912 Human | P04229 Human | P20039 Human | Q29974 Human | Q30134 Human | Q30167 Human | Q5Y7A7 Human | Q95IE3 Human | Q9GIY3 Human
Alternative names: 2B1F_HUMAN DR1 DR16 DR5 DR8 DRB1 DRw10 DW2.2/DR2.2 FLJ75017 FLJ76359 HLA class II antigen beta chain HLA class II histocompatibility antigen, DR-1 beta chain HLA class II histocompatibility antigen, DRB1-15 beta chain HLA-DR-beta 1 HLA-DR1B HLA-DRB HLA-DRB1 human leucocyte antigen DRB1 Leucocyte antigen DR beta 1 chain leucocyte antigen DRB1 lymphocyte antigen DRB1 major histocompatibility complex, class II, DR beta 1 MHC class II antigen MHC class II antigen DRB1*15 MHC class II antigen HLA-DR13 MHC class II HLA-DR beta 1 chain MHC class II HLA-DR-beta cell surface glycoprotein MHC class II HLA-DRw10-beta SS1
Images
HA721927_1.jpg Fig1: Western blot analysis of HLA Class II DRB1 on different lysates with Rabbit anti-HLA Class II DRB1 antibody (HA721927) at 1/1,000 dilution.

Lane 1: Ramos cell lysate
Lane 2: Raji cell lysate
Lane 3: Daudi cell lysate
Lane 4: HDLM-2 cell lysate
Lane 5: A375 cell lysate
Lane 6: HeLa cell lysate (negative)

Lysates/proteins at 20 µg/Lane.

Predicted band size: 29 kDa
Observed band size: 29 kDa

Exposure time: 1 minute;

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 (HA721927) at 1/1,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature.
HA721927_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded human tonsil tissue with Rabbit anti-HLA Class II DRB1 antibody (HA721927) at 1/1,000 dilution.

The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA721927) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
HA721927_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded human skin tissue with Rabbit anti-HLA Class II DRB1 antibody (HA721927) at 1/1,000 dilution.

The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA721927) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
HA721927_4.jpg Fig4: Immunohistochemical analysis of paraffin-embedded human diffuse large B-cell lymphoma tissue with Rabbit anti-HLA Class II DRB1 antibody (HA721927) at 1/1,000 dilution.

The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA721927) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
HA721927_5.jpg Fig5: Immunofluorescence analysis of paraffin-embedded human skin tissue labeling HLA Class II DRB1 with Rabbit anti-HLA Class II DRB1 antibody (HA721927) at 1/100 dilution.

The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 10% negative goat serum for 1 hour at room temperature, washed with PBS, and then probed with the primary antibody (HA721927, green) at 1/100 dilution overnight at 4 ℃, washed with PBS. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. Nuclei were counterstained with DAPI (blue).
HA721927_6.jpg Fig6: Immunofluorescence analysis of paraffin-embedded human diffuse large B-cell lymphoma tissue labeling HLA Class II DRB1 with Rabbit anti-HLA Class II DRB1 antibody (HA721927) at 1/100 dilution.

The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 10% negative goat serum for 1 hour at room temperature, washed with PBS, and then probed with the primary antibody (HA721927, green) at 1/100 dilution overnight at 4 ℃, washed with PBS. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. Nuclei were counterstained with DAPI (blue).
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.