Anti-CD34 antibody [RM2052] - BSA and Azide free
- Advanced Validation
- BOND RX™ Validated
- Recombinant
- RabMAb
- 각 태그의 뜻
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Rabbit Recombinant Multiclonal CD34 antibody. Carrier free. Suitable for Flow Cyt, mIHC, WB, IHC-P, ICC/IF and reacts with Human, Mouse, Rat samples.
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CD34, Hematopoietic progenitor cell antigen CD34
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-CD34 antibody [RM2052] - BSA and Azide free (AB317589)
This data was developed using ab317588, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized KG-1a (human bone marrow myeloblast) cells labelling CD34 with ab317588 at 1/50 (9.88 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2 ug/ml dilution (Green).
Confocal image showing positive staining in KG-1a cell line (shown in green). The counterstain was observed in magenta. Nuclear DNA was labeled with DAPI (shown in blue).
Low expression : Daudi (PMID : 21286385).
Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 2.5ug/ml dilution (Magenta). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/ml dilution.
- mIHC
Lab
Multiplex immunohistochemistry - Anti-CD34 antibody [RM2052] - BSA and Azide free (AB317589)
This data was developed using ab317588, the same antibody clone in a different buffer formulation.
Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded human kidney tissue staining CD34 with ab317588 at a 1/2000 dilution, ab199975 anti-Aquaporin 2 used at 1/4000 dilution and ab212197 anti-Renin used at a 1/4000 dilution.
Panel A : merged staining of anti-CD34 (green; Opal™520), anti-Aquaporin 2 (magenta; Opal™690) and anti-Renin (gray; Opal™570) on human kidney.
Panel B : anti-CD34 staining endothelium in human kidney.
Panel C : anti-Aquaporin 2 staining collecting tubules in human kidney.
Panel D : anti-Renin staining juxtaglomerular cells in human kidney.
Nuclear DNA was labeled with DAPI (shown in blue).
The section was incubated in three rounds of staining : in the order of ab317588, ab199975 and ab212197 for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument with an Opal™ 4-color kit. Image acquisition was performed with Leica SP8 confocal microscope.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CD34 antibody [RM2052] - BSA and Azide free (AB317589)
This data was developed using ab317588, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human placenta tissue labeling CD34 with ab317588 at 1/2000 (0.247 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on endothelium of human placenta (PMID : 35263417). The section was incubated with ab317588 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
- Flow Cyt
Supplier Data
Flow Cytometry - Anti-CD34 antibody [RM2052] - BSA and Azide free (AB317589)
This data was developed using ab317588, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of Daudi(human Burkitt's lymphoma lymphoblast, Left) / KG-1a(human bone marrow myeloblast, Right) cells labelling CD34 with ab317588 at 1/500 dilution (0.1 ug)/Red compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue).
Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/5000 dilution was used as the secondary antibody.
Gated on viable cell.
Low expression : Daudi.
- mIHC
Lab
Multiplex immunohistochemistry - Anti-CD34 antibody [RM2052] - BSA and Azide free (AB317589)
This data was developed using ab317588, the same antibody clone in a different buffer formulation.
Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded human kidney tissue staining CD34 with ab317588 at a 1/2000 dilution, ab321787 anti-SGLT1 used at 1/2000 dilution and ab212197 anti-Renin used at a 1/4000 dilution.
Panel A : merged staining of anti-CD34 (green; Opal™520), anti-SGLT1 (magenta; Opal™690) and anti-Renin (gray; Opal™570) on human kidney.
Panel B : anti-CD34 staining endothelium in human kidney.
Panel C : anti-SGLT1 staining tubules in human kidney.
Panel D : anti-Renin staining juxtaglomerular cells in human kidney.
Nuclear DNA was labeled with DAPI (shown in blue).
The section was incubated in three rounds of staining : in the order of ab317588, ab321787 and ab212197 for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument with an Opal™ 4-color kit. Image acquisition was performed with Leica SP8 confocal microscope.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CD34 antibody [RM2052] - BSA and Azide free (AB317589)
This data was developed using ab317588, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human colon cancer tissue labeling CD34 with ab317588 at 1/2000 (0.247 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on endothelium of human colon cancer. The section was incubated with ab317588 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CD34 antibody [RM2052] - BSA and Azide free (AB317589)
This data was developed using ab317588, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human kidney tissue labeling CD34 with ab317588 at 1/2000 (0.247 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on endothelium of human kidney (PMID : 16234507). The section was incubated with ab317588 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
- Flow Cyt
Supplier Data
Flow Cytometry - Anti-CD34 antibody [RM2052] - BSA and Azide free (AB317589)
This data was developed using ab317588, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of Neuro-2a(mouse neuroblastoma neuroblast, Left) / NIH/3T3(mouse embryonic fibroblast, Right) cells labelling CD34 with ab317588 at 1/50 dilution (1 ug)/Red compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue).
Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/5000 dilution was used as the secondary antibody.
Gated on viable cell.
Low expression : Neuro-2a.
- mIHC
Lab
Multiplex immunohistochemistry - Anti-CD34 antibody [RM2052] - BSA and Azide free (AB317589)
This data was developed using ab317588, the same antibody clone in a different buffer formulation.
Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded mouse kidney tissue staining CD34 with ab317588 at a 1/5000 dilution, ab199975 anti-Aquaporin 2 used at 1/4000 dilution and ab212197 anti-Renin used at a 1/4000 dilution.
Panel A : merged staining of anti-CD34 (green; Opal™520), anti-Aquaporin 2 (magenta; Opal™690) and anti-Renin (gray; Opal™570) on mouse kidney.
Panel B : anti-CD34 staining endothelium in mouse kidney.
Panel C : anti-Aquaporin 2 staining collecting tubules in mouse kidney.
Panel D : anti-Renin staining juxtaglomerular cells in mouse kidney.
Nuclear DNA was labeled with DAPI (shown in blue).
The section was incubated in three rounds of staining : in the order of ab317588, ab199975 and ab212197 for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument with an Opal™ 4-color kit. Image acquisition was performed with Leica SP8 confocal microscope.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
- Flow Cyt
Supplier Data
Flow Cytometry - Anti-CD34 antibody [RM2052] - BSA and Azide free (AB317589)
This data was developed using ab317588, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of Mouse bone marrow cells labelling CD34 with ab317588 at 1/500 dilution (0.1ug)/Right compared with a Rabbit monoclonal IgG (ab172730) / Left isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue).
Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/5000 dilution was used as the secondary antibody.
Mouse bone marrow are co-stained with CD117 conjugated APC-eFluor 780.
Gated on viable cell.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CD34 antibody [RM2052] - BSA and Azide free (AB317589)
This data was developed using ab317588, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Rat lung tissue labeling CD34 with ab317588 at 1/5000 (0.099 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on endothelium of rat lung. The section was incubated with ab317588 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CD34 antibody [RM2052] - BSA and Azide free (AB317589)
This data was developed using ab317588, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse lung tissue labeling CD34 with ab317588 at 1/5000 (0.099 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on endothelium of mouse lung. The section was incubated with ab317588 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CD34 antibody [RM2052] - BSA and Azide free (AB317589)
This data was developed using ab317588, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Rat kidney tissue labeling CD34 with ab317588 at 1/5000 (0.099 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on endothelium of rat kidney. The section was incubated with ab317588 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CD34 antibody [RM2052] - BSA and Azide free (AB317589)
This data was developed using ab317588, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse kidney tissue labeling CD34 with ab317588 at 1/5000 (0.099 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on endothelium of mouse kidney. The section was incubated with ab317588 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins
- WB
Supplier Data
Western blot - Anti-CD34 antibody [RM2052] - BSA and Azide free (AB317589)
This data was developed using ab317588, the same antibody clone in a different buffer formulation.
Low expression : Daudi (PMID : 21286385), HuT-78.
The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID : 37181754, 29296932).
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
All lanes:
Western blot - Anti-CD34 antibody [RM2052] (<a href='/ko/products/primary-antibodies/cd34-antibody-rm2052-ab317588'>ab317588</a>) at 1/1000 dilution
Lane 1:
KG-1a (human bone marrow myeloblast) whole cell lysate at 20 µg
Lane 2:
Daudi (human Burkitts lymphoma lymphoblast) whole cell lysate at 20 µg
Lane 3:
HuT-78 (human Sezary syndrome cutaneous T lymphocyte) whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/ko/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 80-120 kDa,36 kDa
false
Exposure time: 180s
- WB
Supplier Data
Western blot - Anti-CD34 antibody [RM2052] - BSA and Azide free (AB317589)
This data was developed using ab317588, the same antibody clone in a different buffer formulation.
Low expression : liver (PMID : 1709048).
The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID : 37181754, 29296932).
The identity of the lower MW band at approximately 40 kDa (in lane 3) is unknown.
Blocking and diluting buffer and concentration : 5% NFDM/TBST..
Exposure time : Lane 2 : 10 seconds, lanes 1 and 3 : 180 seconds
All lanes:
Western blot - Anti-CD34 antibody [RM2052] (<a href='/ko/products/primary-antibodies/cd34-antibody-rm2052-ab317588'>ab317588</a>) at 1/1000 dilution
Lane 1:
Mouse testis tissue lysate at 20 µg
Lane 2:
Mouse lung tissue lysate at 20 µg
Lane 3:
Mouse liver tissue lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/ko/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 80-120 kDa,36 kDa
true
- WB
Supplier Data
Western blot - Anti-CD34 antibody [RM2052] - BSA and Azide free (AB317589)
This data was developed using ab317588, the same antibody clone in a different buffer formulation.
Low expression : Neuro-2a.
The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID : 37181754, 29296932).
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Exposure time : Lane 1 : 15 seconds, lanes 2-3 : 180 seconds
All lanes:
Western blot - Anti-CD34 antibody [RM2052] (<a href='/ko/products/primary-antibodies/cd34-antibody-rm2052-ab317588'>ab317588</a>) at 1/1000 dilution
Lane 1:
bEnd.3 (mouse brain endothelial cell) whole cell lysate at 20 µg
Lane 2:
NIH/3T3 (mouse embryonic fibroblast) whole cell lysate at 20 µg
Lane 3:
Neuro-2a (mouse neuroblastoma neuroblast) whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/ko/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 80-120 kDa,36 kDa
false
관련 conjugated 항체와 다양한 조성의 항체 (1)
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Anti-CD34 antibody [RM2052]
Reactivity 정보
제품 세부 정보
ab317589 is the carrier-free version of ab317588.
What are recombinant multiclonals?
Recombinant multiclonals are a mixture of recombinant antibodies co-expressed from a library of heavy and light chains. They offer several advantages including:
- - The sensitivity of polyclonal antibodies by recognising multiple epitopes
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
View our range of recombinant multiclonal antibodies.
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
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제품 프로토콜
- Visit the General protocols
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타겟 정보
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com