CRABP1 Recombinant Rabbit Monoclonal Antibody [JE40-53]
cat.: HA722241
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Mouse
Applications: WB, IHC-P, IF-Tissue
Clonality: Monoclonal
Clone number: JE40-53
Form: Liquid
Storage condition: Shipped at 4℃. Store at +4℃ short term (1-2 weeks). Store at -20℃ long term.
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: 15 kDa
Isotype: IgG
Immunogen: Synthetic peptide within Human CRABP1 aa 88-137 / 137.
Positive control: SH-SY5Y cell lysate, Caco-2 cell lysate, NIH/3T3 cell lysate, mouse liver tissue lysate, e14.0 mouse embryonic brain tissue lysate, human breast cancer tissue, human thyroid tissue, mouse embryo tissue.
Subcellular location: Cytoplasm
Recommended Dilutions:
  WB
  IHC-P
  IF-Tissue

1:1,000
1:200-1:1,000
1:50-1:200
Uniprot #: SwissProt: P29762 Human | P62965 Mouse
Alternative names: Cellular retinoic acid binding protein 1 Cellular retinoic acid-binding protein 1 Cellular retinoic acid-binding protein I CRABP 1 CRABP CRABP I CRABP-I Crabp1 CRABPI RABP1_HUMAN RBP 5 RBP5 Retinoic acid binding protein I cellular
Images
HA722241_1.jpg Fig1: Western blot analysis of CRABP1 on different lysates with Rabbit anti-CRABP1 antibody (HA722241) at 1/1,000 dilution.

Lane 1: SH-SY5Y cell lysate (20 µg/Lane)
Lane 2: Caco-2 cell lysate (20 µg/Lane)
Lane 3: NIH/3T3 cell lysate (20 µg/Lane)
Lane 4: Mouse liver tissue lysate (40 µg/Lane)
Lane 5: E14.0 mouse embryonic brain tissue lysate (40 µg/Lane)

Predicted band size: 15 kDa
Observed band size: 15 kDa

Exposure time: 14 seconds; ECL: K1801;
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 (HA722241) 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.
HA722241_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded human breast cancer tissue with Rabbit anti-CRABP1 antibody (HA722241) 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 (HA722241) 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.
HA722241_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded human thyroid tissue with Rabbit anti-CRABP1 antibody (HA722241) 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 (HA722241) 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.
HA722241_4.jpg Fig4: Immunohistochemical analysis of paraffin-embedded mouse embryo tissue with Rabbit anti-CRABP1 antibody (HA722241) 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 (HA722241) 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.
HA722241_5.jpg Fig5: Immunohistochemical analysis of paraffin-embedded mouse spinal cord tissue with Rabbit anti-CRABP1 antibody (HA722241) at 1/200 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 (HA722241) at 1/200 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.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.