• Primary Antibody
  • Secondary Antibodies
  • Lentiviral Particles
  • Stable Cell Lines
  • Lysates
  • Reagents
  • Other Products

KD-Validated Bone Marrow Stromal Cell Antigen 2 Recombinant Rabbit mAb

#61711

Click to copy product information
Recombinant Antibody
Knockdown Validated
Western blotting analysis using bone marrow stromal cell antigen 2 antibody (Cat#61711). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with bone marrow stromal cell antigen 2 antibody (Cat#61711, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Western blotting analysis using bone marrow stromal cell antigen 2 antibody (Cat#61711). Bone marrow stromal cell antigen 2 expression in wild-type (WT) and bone marrow stromal cell antigen 2 (BST2) knockdown (KD) 293T cells with 30 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with bone marrow stromal cell antigen 2 antibody (Cat#61711, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Immunohistochemistry was performed on paraffin-embedded human esophageal carcinoma using bone marrow stromal cell antigen 2 antibody (Cat#61711, 1:200). Antigen retrieval was done in sodium citrate buffer (pH 6.0). DAB was used for detection, with hematoxylin counterstaining. Images were acquired using a Nikon Ci-L Plus microscope (40× objective). Scale bar: 25 μm.
Immunohistochemistry was performed on paraffin-embedded mouse spleen using bone marrow stromal cell antigen 2 antibody (Cat#61711, 1:200). Antigen retrieval was done in sodium citrate buffer (pH 6.0). DAB was used for detection, with hematoxylin counterstaining. Images were acquired using a Nikon Ci-L Plus microscope (40× objective). Scale bar: 25 μm.
Immunocytochemical staining of HepG2 cells with Bone marrow stromal cell antigen 2 antibody (Cat#61711, 1:1,000). Nuclei were stained blue with DAPI; Bone marrow stromal cell antigen 2 was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Medium. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Scale bar, 20 μm.
Flow cytometric analysis of Bone marrow stromal cell antigen 2 expression in HepG2 cells using Bone marrow stromal cell antigen 2 antibody (Cat#61711, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, Bone marrow stromal cell antigen 2.
Please select the specifications of the product.
Specification:
Unit price:
$89.00
Quantity:
1
(Excluding sales tax)
  • Gene Symbol:
    BST2
  • Catalog:
    61711
  • Application:
    WB, FCM, ICC, IHC-P
  • Species Reactivity:
    H, M
Information
Product Name KD-Validated Bone Marrow Stromal Cell Antigen 2 Recombinant Rabbit mAb
Aliases BST2; Bone Marrow Stromal Cell Antigen 2; Tetherin; BST-2; HM1.24; CD317; Bone Marrow Stromal Antigen; Antiviral Factor Tetherin; HM1.24 Antigen; CD317 Antigen; NPC-A-7
Background

Gene Name: BST2

NCBI Gene Entry: 684

UniProt Entry: Q10589

Application Information

Molecular Weight: Predicted, 20 kDa; observed, 28-40 kDa

Clonality: Rabbit monoclonal antibody

Clone ID: 25GB3405

Species Reactivity: Human,mouse

Applications Tested: Western blotting (WB), flow cytometry (FCM), immunocytochemistry (ICC), immunohistochemistry-paraffin (IHC-P)

Immunogen A synthesized peptide derived from human BST2
Isotype Rabbit IgG
Storage Buffer Supplied in PBS (pH 7.4) containing 50% glycerol, and 0.02% sodium azide.
Storage Store at -20 °C for one year.
Recommended Dilutions Western Blotting (WB): 1:1,000-1:5,000
Flow Cytometry (FCM): 1:200-1:2,000
Immunocytochemistry (ICC): 1:100-1:1,000
Immunohistochemistry-Paraffin (IHC-P): 1:100-1:200
Note This product is for research use only.
Data
  • Western blotting analysis using bone marrow stromal cell antigen 2 antibody (Cat#61711). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with bone marrow stromal cell antigen 2 antibody (Cat#61711, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
  • Western blotting analysis using bone marrow stromal cell antigen 2 antibody (Cat#61711). Bone marrow stromal cell antigen 2 expression in wild-type (WT) and bone marrow stromal cell antigen 2 (BST2) knockdown (KD) 293T cells with 30 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with bone marrow stromal cell antigen 2 antibody (Cat#61711, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
  • Immunohistochemistry was performed on paraffin-embedded human esophageal carcinoma using bone marrow stromal cell antigen 2 antibody (Cat#61711, 1:200). Antigen retrieval was done in sodium citrate buffer (pH 6.0). DAB was used for detection, with hematoxylin counterstaining. Images were acquired using a Nikon Ci-L Plus microscope (40× objective). Scale bar: 25 μm.
  • Immunohistochemistry was performed on paraffin-embedded mouse spleen using bone marrow stromal cell antigen 2 antibody (Cat#61711, 1:200). Antigen retrieval was done in sodium citrate buffer (pH 6.0). DAB was used for detection, with hematoxylin counterstaining. Images were acquired using a Nikon Ci-L Plus microscope (40× objective). Scale bar: 25 μm.
  • Immunocytochemical staining of HepG2 cells with Bone marrow stromal cell antigen 2 antibody (Cat#61711, 1:1,000). Nuclei were stained blue with DAPI; Bone marrow stromal cell antigen 2 was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Medium. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Scale bar, 20 μm.
  • Flow cytometric analysis of Bone marrow stromal cell antigen 2 expression in HepG2 cells using Bone marrow stromal cell antigen 2 antibody (Cat#61711, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, Bone marrow stromal cell antigen 2.
Western blotting analysis using bone marrow stromal cell antigen 2 antibody (Cat#61711). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with bone marrow stromal cell antigen 2 antibody (Cat#61711, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Western blotting analysis using bone marrow stromal cell antigen 2 antibody (Cat#61711). Bone marrow stromal cell antigen 2 expression in wild-type (WT) and bone marrow stromal cell antigen 2 (BST2) knockdown (KD) 293T cells with 30 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with bone marrow stromal cell antigen 2 antibody (Cat#61711, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Immunohistochemistry was performed on paraffin-embedded human esophageal carcinoma using bone marrow stromal cell antigen 2 antibody (Cat#61711, 1:200). Antigen retrieval was done in sodium citrate buffer (pH 6.0). DAB was used for detection, with hematoxylin counterstaining. Images were acquired using a Nikon Ci-L Plus microscope (40× objective). Scale bar: 25 μm.
Immunohistochemistry was performed on paraffin-embedded mouse spleen using bone marrow stromal cell antigen 2 antibody (Cat#61711, 1:200). Antigen retrieval was done in sodium citrate buffer (pH 6.0). DAB was used for detection, with hematoxylin counterstaining. Images were acquired using a Nikon Ci-L Plus microscope (40× objective). Scale bar: 25 μm.
Immunocytochemical staining of HepG2 cells with Bone marrow stromal cell antigen 2 antibody (Cat#61711, 1:1,000). Nuclei were stained blue with DAPI; Bone marrow stromal cell antigen 2 was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Medium. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Scale bar, 20 μm.
Flow cytometric analysis of Bone marrow stromal cell antigen 2 expression in HepG2 cells using Bone marrow stromal cell antigen 2 antibody (Cat#61711, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, Bone marrow stromal cell antigen 2.
  • Phone Number

    +1 (301) 545-2395

  • Email Address

    support@genuinbiotech.com

    sales@genuinbiotech.com

  • Office Hours

    8:30 AM - 5:30 PM EST Mon-Fri

微信公众号

Copyright © 2025 Hefei GenuIN Biotech Co., Ltd.

All Rights Reserved.