FAM62B Mouse Monoclonal Antibody [C4-D0]
cat.: M1009-1
Product Type: Mouse monoclonal IgG1, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: IHC-P
Clonality: Monoclonal
Clone number: C4-D0
Form: Liquid
Storage condition: Shipped at 4℃. Store at +4℃ short term (1-2 weeks). It is recommended to aliquot into single-use upon delivery. Store at -20℃ long term.
Storage buffer: 1*TBS (pH7.4), 0.2% BSA, 50% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 2ug/ul
Purification: Protein G affinity purified.
Molecular weight: Predicted band size: 102 kDa
Isotype: IgG1
Immunogen: Recombinant protein within human FAM62B aa 300-550.
Positive control: Human colon cancer tissue, human kidney tissue.
Subcellular location: Cell membrane, Endoplasmic reticulum, Membrane.
Recommended Dilutions:
  IHC-P

1:200
Uniprot #: SwissProt: A0FGR8 Human
Alternative names: Chr2 synaptotagmin CHR2SYT E Syt2 ESYT 2 ESYT2 Extended synaptotagmin 2 Extended synaptotagmin like protein 2 FAM 62B Family with sequence similarity 62 (C2 domain containing) member B Family with sequence similarity 62 member B KIAA1228 Protein FAM62B
Images
M1009-1_1.jpg Fig1: Immunohistochemical analysis of paraffin-embedded human colon cancer tissue with Mouse anti-FAM62B antibody (M1009-1) 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 (M1009-1) 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.
M1009-1_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded human kidney tissue with Mouse anti-FAM62B antibody (M1009-1) 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 (M1009-1) 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”.