MSR1 / CD204 Recombinant Rabbit Monoclonal Antibody [PSH29-03]
cat.: HA752136
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Mouse
Applications: WB, IF-Cell, IHC-P, FC, IP
Clonality: Monoclonal
Clone number: PSH29-03
Form: Liquid
Storage condition: Store at 2-8℃. Avoid freeze.
Storage buffer: PBS (pH7.4).
Concentration: 1ug/ul
Purification: Protein A affinity purified.
Molecular weight: Predicted band size: 50 kDa
Isotype: IgG
Immunogen: Recombinant protein within mouse MRS1 aa 79-458.
Positive control: RAW264.7 (Mouse monocytic macrophage leukemia cell) cell lysate, RAW264.7 treated with 50nM PMA and 5μg/mL Lipopolysaccharide for 24 hours cell lysate, J774A.1 (Mouse monocyte macrophage) cell lysate.
Subcellular location: Membrane.
Uniprot #: SwissProt: P30204 Mouse
Alternative names: CD204 CD204 antigen Macrophage acetylated LDL receptor I and II Macrophage scavenger receptor 1 Macrophage scavenger receptor type III Macrophage scavenger receptor types I and II Msr 1 MSR1 phSR1 phSR2 SCARA 1 SCARA1 Scavenger receptor class A member 1 Scavenger receptor class A, member 1 Scavenger receptor type A Scvr SR A SRA
Images
HA752136_1.JPG Fig1: This data was developed using HA752136, the same antibody clone in a different buffer formulation.
Western blot analysis of MSR1 / CD204 on different lysates with Rabbit anti-MSR1 / CD204 antibody (HA752136) at 1/5,000 dilution.

Lane 1: RAW264.7 (Mouse monocytic macrophage leukemia cell) cell lysate
Lane 2: RAW264.7 treated with 50nM PMA and 5μg/mL Lipopolysaccharide for 24 hours cell lysate

Lysates/proteins at 20 µg/Lane.
Exposure time: 3 minutes; ECL: K1801

Blocking: 5% NFDM/TBST, 1 hour at room temperature
Primary antibody: HA752136, 1/5,000 in primary antibody dilution buffer (K1803), overnight at 4 °C
Secondary antibody: Goat anti-Rabbit IgG-HRP (HA1001), 1/50,000 in 5% NFDM/TBST, 1 hour at room temperature

Predicted band size: 50 kDa
Observed band size: 70-90 kDa
HA752136_2.jpg Fig2: This data was developed using HA752136, the same antibody clone in a different buffer formulation.
Western blot analysis of MSR1 / CD204 on different lysates with Rabbit anti-MSR1 / CD204 antibody (HA752136) at 1/5,000 dilution.

Lane 1: J774A.1 (Mouse monocyte macrophage) cell lysate
Lane 2: Neuro-2a (Mouse brain neuroblastoma cell) cell lysate
Lane 3: NIH/3T3 (Mouse fibroblast) cell lysate

Lysates/proteins at 30 µg/Lane.
Exposure time: 3 minutes; ECL: K1802

Negative control: Neuro-2a, NIH/3T3 (PMID: 35937296).

Blocking: 5% NFDM/TBST, 1 hour at room temperature
Primary antibody: HA752136, 1/5,000 in primary antibody dilution buffer (K1803), overnight at 4 °C
Secondary antibody: Goat anti-Rabbit IgG-HRP (HA1001), 1/50,000 in 5% NFDM/TBST, 1 hour at room temperature

Predicted band size: 50 kDa
Observed band size: 70-90 kDa
HA752136_3.jpg Fig3: This data was developed using HA752136, the same antibody clone in a different buffer formulation.
Application: Immunocytochemistry (IF-cell)

Species: Mouse
Sample: RAW264.7 (Mouse monocytic macrophage leukemia cell) treated with or without 50 nM PMA and 5 μg/mL LPS for 24 hours

Fixation: 4% Paraformaldehyde, 15 minutes at room temperature.
Permeabilization: 0.1% Triton X-100, 15 minutes at room temperature.
Blocking: 1% BSA + 10% normal goat serum, 1 hour at room temperature.
Antibody dilution buffer: 1% BSA in PBST.

Primary antibody: HA752136, 1/5,000, overnight at 4°C.
Secondary antibody: Goat Anti-Rabbit IgG (iFluor™ 488, HA1121), 45 minutes at room temperature.
Counterstain: Beta tubulin (HA601187, Red), 1/100, overnight at 4℃. The nuclear counterstain was DAPI (Blue).
HA752136_4.jpg Fig4: This data was developed using HA752136, the same antibody clone in a different buffer formulation.
Application: Immunocytochemistry (IF-cell)

Species: Mouse
Sample: J774A.1 (Mouse monocyte macrophage) / NIH/3T3 (Mouse fibroblast)

Fixation: 4% Paraformaldehyde, 15 minutes at room temperature.
Permeabilization: 0.1% Triton X-100, 15 minutes at room temperature.
Blocking: 1% BSA + 10% normal goat serum, 1 hour at room temperature.
Antibody dilution buffer: 1% BSA in PBST.

Primary antibody: HA752136, 1/500, overnight at 4℃.
Secondary antibody: Goat Anti-Rabbit IgG (iFluor™ 488, HA1121), 45 minutes at room temperature.
Counterstain: Beta tubulin (HA601187, Red), 1/100, overnight at 4℃. The nuclear counterstain was DAPI (Blue).

Negative control: NIH/3T3 (PMID: 35937296).
HA752136_5.jpg Fig5: This data was developed using HA752136, the same antibody clone in a different buffer formulation.
Application: Immunohistochemistry (IHC-P)

Species: Mouse
Tissue: Thymus
Sample: Paraffin-embedded section

Antigen retrieval: Heat-mediated, Tris-EDTA buffer (pH 9.0), 20 minutes at 95°C.

Wash buffer: 1× TBST
Endogenous peroxidase blocking: 3% H₂O₂, 10 minutes at room temperature.
Blocking: 1% BSA + 10% normal goat serum, 10 minutes at room temperature.
Primary antibody: HA752136, 1/200, 1 hour at room temperature.
Secondary antibody: HA1119, 20 minutes at room temperature.
HA752136_6.jpg Fig6: This data was developed using HA752136, the same antibody clone in a different buffer formulation.
Application: Immunohistochemistry (IHC-P)

Species: Mouse
Tissue: Spleen
Sample: Paraffin-embedded section

Antigen retrieval: Heat-mediated, Tris-EDTA buffer (pH 9.0), 20 minutes at 95°C.

Wash buffer: 1× TBST
Endogenous peroxidase blocking: 3% H₂O₂, 10 minutes at room temperature.
Blocking: 1% BSA + 10% normal goat serum, 10 minutes at room temperature.
Primary antibody: HA752136, 1/200, 1 hour at room temperature.
Secondary antibody: HA1119, 20 minutes at room temperature.
HA752136_7.jpg Fig7: This data was developed using HA752136, the same antibody clone in a different buffer formulation.
Application: Immunohistochemistry (IHC-P)

Species: Mouse
Tissue: Colon
Sample: Paraffin-embedded section

Antigen retrieval: Heat-mediated, Tris-EDTA buffer (pH 9.0), 20 minutes at 95°C.

Wash buffer: 1× TBST
Endogenous peroxidase blocking: 3% H₂O₂, 10 minutes at room temperature.
Blocking: 1% BSA + 10% normal goat serum, 10 minutes at room temperature.
Primary antibody: HA752136, 1/200, 1 hour at room temperature.
Secondary antibody: HA1119, 20 minutes at room temperature.
HA752136_8.jpg Fig8: This data was developed using HA752136, the same antibody clone in a different buffer formulation.
Application: Immunohistochemistry (IHC-P)

Species: Mouse
Tissue: RAW264.7 (Mouse monocytic macrophage leukemia cell)
Sample: Paraffin-embedded section

Antigen retrieval: Heat-mediated, Tris-EDTA buffer (pH 9.0), 20 minutes at 95°C.

Wash buffer: 1× TBST
Endogenous peroxidase blocking: 3% H₂O₂, 10 minutes at room temperature.
Blocking: 1% BSA + 10% normal goat serum, 10 minutes at room temperature.
Primary antibody: HA752136, 1/1,000, 1 hour at room temperature.
Secondary antibody: HA1119, 20 minutes at room temperature.
HA752136_9.jpg Fig9: This data was developed using HA752136, the same antibody clone in a different buffer formulation.
Application: Immunohistochemistry (IHC-P)

Species: Mouse
Tissue: J774A.1 (Mouse monocyte macrophage)
Sample: Paraffin-embedded section

Antigen retrieval: Heat-mediated, Tris-EDTA buffer (pH 9.0), 20 minutes at 95°C.

Wash buffer: 1× TBST
Endogenous peroxidase blocking: 3% H₂O₂, 10 minutes at room temperature.
Blocking: 1% BSA + 10% normal goat serum, 10 minutes at room temperature.
Primary antibody: HA752136, 1/1,000, 1 hour at room temperature.
Secondary antibody: HA1119, 20 minutes at room temperature.
HA752136_10.jpg Fig10: This data was developed using HA752136, the same antibody clone in a different buffer formulation.
Application: Immunohistochemistry (IHC-P)

Species: Mouse
Tissue: Neuro-2a (Mouse brain neuroblastoma cell)
Sample: Paraffin-embedded section

Negative control: Neuro-2a (PMID: 35937296).

Antigen retrieval: Heat-mediated, Tris-EDTA buffer (pH 9.0), 20 minutes at 95°C.

Wash buffer: 1× TBST
Endogenous peroxidase blocking: 3% H₂O₂, 10 minutes at room temperature.
Blocking: 1% BSA + 10% normal goat serum, 10 minutes at room temperature.
Primary antibody: HA752136, 1/1,000, 1 hour at room temperature.
Secondary antibody: HA1119, 20 minutes at room temperature.
HA752136_11.jpg Fig11: This data was developed using HA752136, the same antibody clone in a different buffer formulation.
Application: Flow Cytometry

Species: Mouse
Sample: NIH/3T3 (Mouse fibroblasts) (Left, negative) / J774A.1 (Mouse monocyte macrophage)

Blocking: 1% BSA + 10% normal goat serum, 15 minutes at room temperature.
Antibody dilution buffer: 1x PBS.

Primary antibody: HA752136(1/1,000, Red) compared with Rabbit IgG Isotype Control (HA722127, Green), 15 minutes at room temperature.
Secondary antibody: Goat Anti-Rabbit IgG (iFluor™ 488, HA1121), 15 minutes at room temperature.

Negative control: NIH/3T3 (PMID: 35937296).
HA752136_12.jpg Fig12: This data was developed using HA752136, the same antibody clone in a different buffer formulation.
Immunoprecipitation (IP)

MSR1 / CD204 was immunoprecipitated in 0.2 mg RAW264.7 (Mouse monocytic macrophage leukemia cell) treated with 50nM PMA and 5μg/mL LPS for 24 hours cell lysate with HA752136 at 2 µg/10 µl beads. Western blot was performed from the immunoprecipitate using HA752136 at 1/5,000 dilution. Anti-Rabbit IgG for IP, AlpSdAbs® VHH(HRP) (025-100-005) at 1/5,000 dilution was used for 1 hour at room temperature.

Lane 1: RAW264.7 treated with 50nM PMA and 5μg/mL LPS for 24 hours cell lysate (input)
Lane 2: HA752136 IP in RAW264.7 treated with 50nM PMA and 5μg/mL LPS for 24 hours cell lysate
Lane 3: Rabbit IgG instead of HA752136 in RAW264.7 treated with 50nM PMA and 5μg/mL LPS for 24 hours cell lysate

Exposure time: 2 seconds
Blocking: 5% NFDM/TBST, 1 hour at room temperature

Primary dilution: HA752136, 1/5,000 in primary antibody dilution buffer (K1803), 2 hours at room temperature

Predicted band size: 50 kDa
Observed band size: 70-90 kDa
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.