Anti-CD5L/CT-2 antibody [EPR29363-540]
- BOND RX™ Validated
- Recombinant
- 20ul selling size
- RabMAb
- Advanced Validation
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Rabbit Recombinant Monoclonal CD5L/CT-2 antibody. Suitable for mIHC, IHC-P, WB and reacts with Human samples.
View Alternative Names
API6, UNQ203/PRO229, CD5L, CD5 antigen-like, Apoptosis inhibitor expressed by macrophages, CT-2, IgM-associated peptide, SP-alpha, hAIM
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CD5L/CT-2 antibody [EPR29363-540] (AB323268)
Immunohistochemical analysis of paraffin-embedded Human liver tissue labeling CD5L/CT-2 with ab323268 at 1/2000 (0.246 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on kupffer cells of human liver. The section was incubated with ab323268 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background.
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 Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- mIHC
Lab
Multiplex immunohistochemistry - Anti-CD5L/CT-2 antibody [EPR29363-540] (AB323268)
Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded human liver cancer tissue staining CD5L with ab323268 at a 1/2000 dilution (0.246 μg/ml) and CD68 with ab213363 at 1/500 dilution (1.26 μg/ml), followed by a ready to use secondary antibody Opal Polymer HRP Ms + Rb.
Panel A : merged staining of anti-CD5L (green; Opal™520) and anti-CD68 (magenta; Opal™690) on human liver cancer.
Panel B : anti-CD5L staining Kupffer cells in human liver cancer.
Panel C : anti-CD68 staining Kupffer cells in human liver cancer.
Panel D : Nuclear DNA was labeled with DAPI (shown in blue).
The section was incubated in three rounds of staining : in the order of ab323268 and ab213363 for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
- mIHC
Lab
Multiplex immunohistochemistry - Anti-CD5L/CT-2 antibody [EPR29363-540] (AB323268)
Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded human spleen tissue staining CD5L with ab323268 at a 1/2000 dilution (0.246 μg/ml) and CD68 with ab213363 at 1/500 dilution (1.26 μg/ml), followed by a ready to use secondary antibody Opal Polymer HRP Ms + Rb.
Panel A : merged staining of anti-CD5L (green; Opal™520) and anti-CD68 (magenta; Opal™690) on human spleen.
Panel B : anti-CD5L staining Kupffer cells in human spleen.
Panel C : anti-CD68 staining Kupffer cells in human spleen.
Panel D : Nuclear DNA was labeled with DAPI (shown in blue).
The section was incubated in three rounds of staining : in the order of ab323268 and ab213363 for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
- mIHC
Lab
Multiplex immunohistochemistry - Anti-CD5L/CT-2 antibody [EPR29363-540] (AB323268)
Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded human liver tissue staining CD5L with ab323268 at a 1/2000 dilution (0.246 μg/ml) and CD68 with ab213363 at 1/500 dilution (1.26 μg/ml), followed by a ready to use secondary antibody Opal Polymer HRP Ms + Rb.
Panel A : merged staining of anti-CD5L (green; Opal™520) and anti-CD68 (magenta; Opal™690) on human liver.
Panel B : anti-CD5L staining Kupffer cells in human liver.
Panel C : anti-CD68 staining Kupffer cells in human liver.
Panel D : Nuclear DNA was labeled with DAPI (shown in blue).
The section was incubated in three rounds of staining : in the order of ab323268 and ab213363 for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.
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-CD5L/CT-2 antibody [EPR29363-540] (AB323268)
Immunohistochemical analysis of paraffin-embedded Human testis tissue labeling CD5L/CT-2 with ab323268 at 1/2000 (0.246 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Low expression : weak staining on some scattered cells in human testis. The section was incubated with ab323268 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background.
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 Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CD5L/CT-2 antibody [EPR29363-540] (AB323268)
Immunohistochemical analysis of paraffin-embedded Human skeletal muscle tissue labeling CD5L/CT-2 with ab323268 at 1/2000 (0.246 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Low expression : no staining on human skeletal muscle. The section was incubated with ab323268 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CD5L/CT-2 antibody [EPR29363-540] (AB323268)
Immunohistochemical analysis of paraffin-embedded Human spleen tissue labeling CD5L/CT-2 with ab323268 at 1/2000 (0.246 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on human spleen. The section was incubated with ab323268 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background.
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 Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CD5L/CT-2 antibody [EPR29363-540] (AB323268)
Immunohistochemical analysis of paraffin-embedded Hepatocellular carcinoma tissue labeling CD5L/CT-2 with ab323268 at 1/2000 (0.246 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on immune cells of hepatocellular carcinoma. The section was incubated with ab323268 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background.
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 Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- WB
Supplier Data
Western blot - Anti-CD5L/CT-2 antibody [EPR29363-540] (AB323268)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Low expression : testis (PMID : 10651944)
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
All lanes:
Western blot - Anti-CD5L/CT-2 antibody [EPR29363-540] (ab323268) at 1/1000 dilution
Lane 1:
Human lung tissue lysate at 40 µg
Lane 2:
Human plasma lysate at 40 µg
Lane 3:
Human testis tissue lysate at 40 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Observed band size: 38 kDa,36 kDa
false
Exposure time: 1s
- WB
Supplier Data
Western blot - Anti-CD5L/CT-2 antibody [EPR29363-540] (AB323268)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Low expression : cerebellum, skeletal muscle (PMID : 10651944)
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
All lanes:
Western blot - Anti-CD5L/CT-2 antibody [EPR29363-540] (ab323268) at 1/1000 dilution
Lane 1:
Human cerebellum tissue lysate at 20 µg
Lane 2:
Human liver tissue lysate at 20 µg
Lane 3:
Human skeletal muscle tissue lysate at 20 µg
Lane 4:
Human spleen tissue lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Observed band size: 38 kDa,36 kDa
false
Exposure time: 6s
Reactivity data
Product details
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.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Properties and storage information
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Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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