CD180 Rabbit Polyclonal Antibody
cat.: ER2001-06
Product Type: Rabbit polyclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
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*TBS (pH7.4), 0.2% BSA, 50% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1ug/ul
Purification: Immunogen affinity purified.
Molecular weight: Predicted band size: 74 kDa.
Isotype: IgG
Immunogen: Recombinant protein within human CD180 aa 370-580.
Positive control: Daudi cell lysate, rat spleen tissue lysate, mouse spleen tissue lysate, rat spleen tissue, human spleen tissue, mouse spleen tissue, Daudi.
Subcellular location: Cell membrane.
Recommended Dilutions:
  WB
  IHC-P
  FC
1:500-1:2,000
1:50-1:200
1:50-1:100
Uniprot #: SwissProt: Q99467 Human | Q62192 Mouse
Alternative names: CD180 CD180 antigen CD180_HUMAN F630107B15 LY64 Ly78 Lymphocyte antigen 64 lymphocyte antigen 64 radioprotective 105kDa lymphocyte antigen-64, radioprotective, 105kDa MGC126233 MGC126234 Radioprotective 105 kDa protein RP105
Images
ER2001-06_1.jpg Fig1: Western blot analysis of CD180 on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (ER2001-06, 1/500) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:5,000 dilution was used for 1 hour at room temperature.
Positive control:
Lane 1: Daudi cell lysate
Lane 2: Rat spleen tissue lysate
Lane 3: Mouse spleen tissue lysate
ER2001-06_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded rat spleen tissue using anti-CD180 antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ER2001-06, 1/50) for 30 minutes 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.
ER2001-06_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded human spleen tissue using anti-CD180 antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ER2001-06, 1/200) for 30 minutes 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.
ER2001-06_4.jpg Fig4: Immunohistochemical analysis of paraffin-embedded mouse spleen tissue using anti-CD180 antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ER2001-06, 1/200) for 30 minutes 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.
ER2001-06_5.jpg Fig5: Flow cytometric analysis of CD180 was done on Daudi cells. The cells were fixed, permeabilized and stained with the primary antibody (ER2001-06, 1/50) (red). After incubation of the primary antibody at room temperature for an hour, the cells were stained with a Alexa Fluor 488-conjugated Goat anti-Rabbit IgG Secondary antibody at 1/1000 dilution for 30 minutes.Unlabelled sample was used as a control (cells without incubation with primary antibody; black).
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.