Carboxypeptidase A1+A2+B Recombinant Rabbit Monoclonal Antibody [JE34-07]
cat.: HA722393
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IHC-P
Clonality: Monoclonal
Clone number: JE34-07
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: 47 kDa
Isotype: IgG
Immunogen: Synthetic peptide.
Positive control: Mouse pancreas tissue lysate, rat pancreas tissue lysate, human pancreas tissue, mouse pancreas tissue, rat pancreas tissue.
Subcellular location: Secreted.
Recommended Dilutions:
  WB
  IHC-P

1:1,000
1:200-1:1,000
Uniprot #: SwissProt: P15085 Human | P48052 Human | P15086 Human | Q7TPZ8 Mouse | P00731 Rat | P19222 Rat | P19223 Rat
Alternative names: carboxypeptidase A1 (pancreatic) Carboxypeptidase A1 Carboxypeptidase A1 precursor CBPA1_HUMAN CPA CPA1 Pancreatic carboxypeptidase A1 Procarboxypeptidase A1 pancreatic Carboxypeptidase A2 CPA2 Carboxypeptidase B Carboxypeptidase B1 (tissue) Carboxypeptidase B1 CarboxypeptidaseB CarboxypeptidaseB1 CBPB1_HUMAN CP B1 CPB 1 CPB CPB1 DKFZp779K1333 Pancreas specific protein Pancreas-specific protein Pancreatic carboxypeptidase B Pancreatic carboxypeptidase B1 PASP PCPB Procarboxypeptidase B Procarboxypeptidase B pancreatic Protaminase Tissue carboxypeptidase B
Images
HA722393_1.jpg Fig1: Western blot analysis of Carboxypeptidase A1+A2+B on different lysates with Rabbit anti-Carboxypeptidase A1+A2+B antibody (HA722393) at 1/1,000 dilution.

Lane 1: Mouse pancreas tissue lysate
Lane 2: Rat pancreas tissue lysate

Lysates/proteins at 30 µg/Lane.

Predicted band size: 47 kDa
Observed band size: 43 kDa

Exposure time: 3 minutes; ECL: K1802;
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 (HA722393) 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.
HA722393_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded human pancreas tissue with Rabbit anti-Carboxypeptidase A1+A2+B antibody (HA722393) 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 (HA722393) 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.
HA722393_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded mouse pancreas tissue with Rabbit anti-Carboxypeptidase A1+A2+B antibody (HA722393) 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 (HA722393) 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.
HA722393_4.jpg Fig4: Immunohistochemical analysis of paraffin-embedded rat pancreas tissue with Rabbit anti-Carboxypeptidase A1+A2+B antibody (HA722393) 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 (HA722393) 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”.