ACE2 Rabbit Polyclonal Antibody_长沙艾碧维生物科技有限公司

货号：

AWA41459

应用：

IHC-P,IF-T,ELISA

反应性：

Human,Mouse,Rat

来源：

Rabbit

规格 价格 库存
20μL ¥620 1-3个工作日
50μL ¥1250 1-3个工作日
100μL ¥2200 1-3个工作日

产品概述

Product Details

Host Species:

Rabbit

Reactivity:

Human,Mouse,Rat

Molecular Wt:

92 kDa

Clonality:

Polyclonal

Isotype:

IgG

Concentration:

1 mg/ml

Other Names:

ACE2; Angiotensin-converting enzyme 2; ACE-related carboxypeptidase; ACE related carboxypeptidase; Angiotensin converting enzyme 2; Angiotensin I converting enzyme 2; Angiotensin-converting enzyme homolog; ACEH; Metalloprotease MPROT15

Formulation:

Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

Purification:

Affinity-chromatography

Storage:

-20°C,1 year

Applications

IHC-P 1:200

IF-T 1:200

ELISA 1:40000

Immunogen

Information

Gene Name：

ACE2

Protein Name：

Angiotensin-converting enzyme 2

Gene ID：

59272 (Human)

70008 (Mouse)

302668 (Rat)

SwissPro：

Q9BYF1 (Human)

Q8R0I0 (Mouse)

Q5EGZ1 (Rat)

Subcellular Location：

Cell membrane. Cytoplasm. Cell projection, cilium. Apical cell membrane. Secreted.

Immunogen：

The antiserum was produced against synthesized peptide derived from human ACE2. AA range: 416-465.

Specificity:

ACE2 Polyclonal Antibody detects endogenous levels of ACE2 protein.

Product images
	Fig: Fluorescence immunohistochemical analysis of Mouse-Ileum tissue (Formalin/PFA-fixed paraffin-embedded sections). with Rabbit anti-ACE2 antibody (AWA41459) 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 EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 5% BSA for 60 minutes at 37℃, washed with ddH2O and PBS, and then probed with the primary antibody (AWA41459) at 1/200 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system followed by a separate fluorescent tyramide signal amplification system (green). DAPI (blue, AWC0291) was used as a nuclear counter stain. Image acquisition was performed with Slide Scanner.
	Fig: Fluorescence immunohistochemical analysis of Rat-Ileum tissue (Formalin/PFA-fixed paraffin-embedded sections). with Rabbit anti-ACE2 antibody (AWA41459) 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 EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 5% BSA for 60 minutes at 37℃, washed with ddH2O and PBS, and then probed with the primary antibody (AWA41459) at 1/200 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system followed by a separate fluorescent tyramide signal amplification system (green). DAPI (blue, AWC0291) was used as a nuclear counter stain. Image acquisition was performed with Slide Scanner.
	Fig : Immunohistochemical analysis of paraffin-embedded rat-kidney tissue with rabbit anti-ACE2 antibody ( AWA41459 ) 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 (AWA41459) 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.
	Fig : Immunohistochemical analysis of paraffin-embedded rat-spleen tissue with rabbit anti-ACE2 antibody ( AWA41459 ) 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 (AWA41459) 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.