YKL-40/CHI3L1 Mouse Monoclonal Antibody [A3G10]
cat.: EM1902-31
Product Type: Mouse monoclonal IgG2a, primary antibodies
Species reactivity: Human
Applications: WB, IHC-P
Clonality: Monoclonal
Clone number: A3G10
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.
Storage buffer: 1*PBS (pH7.4), 0.2% BSA, 50% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 2 mg/mL.
Purification: Protein G affinity purified.
Molecular weight: 43 kDa
Isotype: IgG2a
Immunogen: Recombinant protein within extracellular domain of Human CHI3L1.
Positive control: THP-1 cell lysates, human tonsil tissue.
Subcellular location: Extracellular space, Endoplasmic reticulum, Cytoplasm.
Recommended Dilutions:
  WB
  IHC-P

1:500-1:2,000
1:50-1:200
Uniprot #: SwissProt: P36222 Human
Alternative names: 39 kDa synovial protein ASRT7 Cartilage glycoprotein 39 CGP-39 CGP39 CH3L1_HUMAN CHI3L1 chitinase 3 like 1 (cartilage glycoprotein 39) chitinase 3 like 1 Chitinase 3 like protein 1 precursor chitinase Chitinase-3-like protein 1 Chondrocyte protein YKL40 GP 39 GP-39 GP39 HC gp39 HCGP 3P hCGP-39 HCgp39 YKL 40 YKL-40 YKL40 YYL 40
Images
EM1902-31_1.jpg Fig1: Western blot analysis of YKL-40/CHI3L1 on THP-1 cell lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (EM1902-31, 1/500) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Mouse IgG - HRP Secondary Antibody (HA1006) at 1:5,000 dilution was used for 1 hour at room temperature.
EM1902-31_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded human tonsil tissue using anti-YKL-40/CHI3L1 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 (EM1902-31, 1/400) 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.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.