EPCAM Recombinant Rabbit Monoclonal Antibody
一键复制产品信息
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- 20μL
- ¥620
- 1-3个工作日
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- 50μL
- ¥1250
- 1-3个工作日
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- 100μL
- ¥2200
- 1-3个工作日
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Product Details |
Host Species: Rabbit |
Reactivity: Human, Mouse, Rat |
Molecular Wt: Predicted MW: 35 kDa | |||
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Clonality: Monoclonal |
Isotype: IgG |
Concentration: 1.185mg/ml | |||
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Other Names: EGP; CO17 1A; CO 17A; Cell surface glycoprotein Trop-1; ESA; KSA; M4S1; MK-1; DIAR5; EGP-2; EGP40; KS1/4; MIC18; TROP1; BerEp4; EGP314; HNPCC8; LYNCH8; MOC-31; Ber-Ep4; TACSTD1; EpCAM; EPCAM | |||||
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Formulation: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. | |||||
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Purification: Affinity-chromatography | |||||
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Storage: Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20°C storage. | |||||
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Applications |
WB 1:1000-1:5000 | |||||
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Immunogen |
Gene Name: EPCAM |
Protein Name: Epithelial cell adhesion molecule | ||||
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Gene ID: 4072 (Human) |
SwissPro: P16422 (Human) | ||||
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Immunogen |
Subcellular Location: Lateral cell membrane. Cell junction, tight junction. | |||||
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Immunogen: Recombinant fragment of human EPCAM. | |||||
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Specificity: EPCAM Monoclonal Antibody detects endogenous levels of EPCAM protein. | |||||
| Product images | |
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Fig: Multiplex immunohistochemistry analysis of Rat-intestinal tissue (Formalin/PFA-fixed paraffin-embedded sections). Merged staining of anti-CD27 (AWA10960; green; TSA-520:AWI0688), anti-HLA-DRA (AWA12675; red; TSA-570: AWI0689), anti-EPCAM (AWA13608; white; TSA-690: AWI0691). Antibody Wash Solution (for mIHC) (AWI0707, 37℃, 20 minutes) was used in between rounds of tyramide signal amplification to remove the antibody from the previous round, to avoid any cross-reactivity. The section was incubated in three rounds of staining; in the order of CD27 (AWA10960) (1/200 dilution), anti-HLA-DRA (AWA12675) (1/200 dilution), anti-EPCAM (AWA13608) (1/200 dilution); each using a separate fluorescent tyramide signal amplification system. DAPI (blue, AWC0291) was used as a nuclear counter stain. Microscopy and pseudocoloring of individual TSA dyes was performed using a pannoramic midi. |
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Fig : Western blot analysis of EPCAM on different lysates. Proteins were transferred to a NC membrane and blocked with 5% NF-Milk in TBST for 1 hour at room temperature. The primary antibody (AWA13608, 1/1000) was used in TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (AWS0002) at 1:5,000 dilution was used for 1 hour at room temperature. Positive control: Lane 1: HCT116 cell Lane 2: HT-29 cell Lane 3: SW620 cell Predicted molecular weight:35 kDa Observed molecular weight:40 kDa |
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Fig: Multiplex immunohistochemistry analysis of Rat-intestinal tissue (Formalin/PFA-fixed paraffin-embedded sections). Merged staining of anti-Cytochrome C (AWA10373; green; TSA-520:AWI0688), anti-EPCAM (AWA13608; red; TSA-570: AWI0689), anti-Lamin B1 (AWA11310; white; TSA-690: AWI0691). Antibody Wash Solution (for mIHC) (AWI0707, 37℃, 20 minutes) was used in between rounds of tyramide signal amplification to remove the antibody from the previous round, to avoid any cross-reactivity. The section was incubated in three rounds of staining; in the order of Cytochrome C (AWA10373) (1/200 dilution), anti-EPCAM (AWA13608) (1/200 dilution), anti-Lamin B1 (AWA11310) (1/200 dilution); each using a separate fluorescent tyramide signal amplification system. DAPI (blue, AWC0291) was used as a nuclear counter stain. Microscopy and pseudocoloring of individual TSA dyes was performed using a pannoramic midi. |
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Fig: Fluorescence immunohistochemical analysis of Rat-ileum tissue (Formalin/PFA-fixed paraffin-embedded sections) with Rabbit anti-EPCAM antibody (AWA13608) at 1/200 dilution.The immunostaining was performed with the TSA Immuno-staining Kit (ABIOWELL, AWI0688). The section was pre-treated using heat mediated antigen retrieval with Sodium citrate buffer (pH 6.0) for 20 minutes. The tissues were blocked in 3% H2O2 for 15 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (AWA13608) at 1/200 dilution for 2 hour at 37℃or overnignt at 4℃. The detection was performed using an HRP conjugated compact polymer system followed by a separate fluorescent tyramide signal amplification system (grenn). DAPI (blue, AWC0291) was used as a nuclear counter stain. Image acquisition was performed with Slide Scanner. |
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Fig : Immunohistochemical analysis of paraffin-embedded Mouse-bladder tissue with Rabbit anti- EPCAM antibody (AWA13608) at 1/200 dilution. The section was pre-treated using heat mediated antigen retrieval with Sodium citrate buffer (pH 6.0) for 20 minutes. The tissues were blocked in 3% H2O2 for 15 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (AWA13608) at 1/200 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system(ABIOWELL, AWI0629). DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX. |
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Fig: Immunocytochemistry analysis of HTC-116 cells labeling EPCAM with Rabbit anti-EPCAM antibody (AWA13608) at 1/300 dilution(Green). Cells were fixed in 4% paraformaldehyde for 10 minutes at 37 ℃, permeabilized with 0.03% Triton X-100 in PBS for 30 minutes, and then blocked with 5% BSA for 60 minutes at 37 ℃. Cells were then incubated with Rabbit anti- EPCAM antibody (AWA13608) at 1/300 dilution in 2% negative goat serum overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, AWS0005) was used as the secondary antibody at 1/200 dilution for 60 minutes at 37 ℃. Nuclear DNA was labelled in blue with DAPI(AWC0291). |
-
-
- 20μL
- ¥620
- 1-3个工作日
-
- 50μL
- ¥1250
- 1-3个工作日
-
- 100μL
- ¥2200
- 1-3个工作日
-
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