Anti-SLC34A2 antibody [EPR30528-645]
- RabMAb
- Recombinant
- 20ul selling size
- Advanced Validation
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Rabbit Recombinant Monoclonal SLC34A2 antibody. Suitable for WB, IHC-P, mIHC and reacts with Transfected cell lysate - Human, Human samples.
View Alternative Names
Sodium-dependent phosphate transport protein 2B, Sodium-phosphate transport protein 2B, Na(+)-dependent phosphate cotransporter 2B, NaPi3b, Sodium/phosphate cotransporter 2B, Solute carrier family 34 member 2, Na(+)/Pi cotransporter 2B, NaPi-2b, SLC34A2
- mIHC
Lab
Multiplex immunohistochemistry - Anti-SLC34A2 antibody [EPR30528-645] (AB325747)
Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded human endometrium tissue staining SLC34A2 with ab325747 at a 1 : 500 (0.99 ug/ml) dilution, ab40772 anti-E Cadherin used at 1 : 1000 (0.325 ug/ml) dilution and ab255609 anti-CD10 used at a 1 : 1000 (0.615 ug/ml) dilution.
Panel A : merged staining of anti-SLC34A2 (green; Opal™520), anti-E Cadherin (magenta; Opal™570) and anti-CD10 (gray; Opal™690) on human endometrium.
Panel B : anti-SLC34A2 staining apical cell membrane of glandular cells in human endometrium.
Panel C : anti-E Cadherin staining glandular cells in human endometrium.
Panel D : anti-CD10 staining stromal cells in human endometrium.
Nuclear DNA was labeled with DAPI (shown in blue).
The section was incubated in three rounds of staining : in the order of ab325747, ab40772 and ab255609 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.
- mIHC
Lab
Multiplex immunohistochemistry - Anti-SLC34A2 antibody [EPR30528-645] (AB325747)
Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded human endometrial cancer tissue staining SLC34A2 with ab325747 at a 1 : 500 (0.99 ug/ml) dilution, ab40772 anti-E Cadherin used at 1 : 1000 (0.325 ug/ml) dilution and ab255609 anti-CD10 used at a 1 : 1000 (0.615 ug/ml) dilution.
Panel A : merged staining of anti-SLC34A2 (green; Opal™520), anti-E Cadherin (magenta; Opal™570) and anti-CD10 (gray; Opal™690) on human endometrial cancer.
Panel B : anti-SLC34A2 staining apical cell membrane of glandular cells in human endometrial cancer.
Panel C : anti-E Cadherin staining glandular cells in human endometrial cancer.
Panel D : anti-CD10 staining stromal cells in human endometrial cancer.
Nuclear DNA was labeled with DAPI (shown in blue).
The section was incubated in three rounds of staining : in the order of ab325747, ab40772 and ab255609 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
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SLC34A2 antibody [EPR30528-645] (AB325747)
Immunohistochemical analysis of paraffin-embedded Human lung carcinoma tissue labeling SLC34A2 with ab325747 at 1/500 (0.99 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on human lung carcinoma. The primary antibody was incubated 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 Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SLC34A2 antibody [EPR30528-645] (AB325747)
Immunohistochemical analysis of paraffin-embedded Human lung tissue labeling SLC34A2 with ab325747 at 1/500 (0.99 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on human lung. The primary antibody was incubated 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 Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SLC34A2 antibody [EPR30528-645] (AB325747)
Immunohistochemical analysis of paraffin-embedded Clear cell carcinoma of human kidney tissue labeling SLC34A2 with ab325747 at 1/500 (0.99 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on clear cell carcinoma of human kidney. The primary antibody was incubated 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 Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SLC34A2 antibody [EPR30528-645] (AB325747)
Immunohistochemical analysis of paraffin-embedded Human ovarian carcinoma tissue labeling SLC34A2 with ab325747 at 1/500 (0.99 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on human ovarian carcinoma. The primary antibody was incubated 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 Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SLC34A2 antibody [EPR30528-645] (AB325747)
Immunohistochemical analysis of paraffin-embedded Human breast tissue labeling SLC34A2 with ab325747 at 1/500 (0.99 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on apical cell membrane of human breast. The primary antibody was incubated 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 Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- WB
Lab
Western blot - Anti-SLC34A2 antibody [EPR30528-645] (AB325747)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Negative control : HepG2, U-2 OS, SUM149PT.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) (1 : 200000) (36KDa).
All lanes:
Western blot - Anti-SLC34A2 antibody [EPR30528-645] (ab325747) at 1/1000 dilution
Lane 1:
NIH:OVCAR-3 (human ovary adenocarcinoma epithelial cell) whole cell lysate at 20 µg
Lane 2:
HepG2 (human hepatocellular carcinoma epithelial cell) whole cell lysate at 20 µg
Lane 3:
SUM149PT (human breast adenocarcinoma cell) whole cell lysate at 20 µg
Lane 4:
U-2 OS (human bone osteosarcoma epithelial cell) whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Observed band size: 75-100 kDa,36 kDa
false
Exposure time: 48s
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SLC34A2 antibody [EPR30528-645] (AB325747)
Immunohistochemical analysis of paraffin-embedded Human liver tissue labeling SLC34A2 with ab325747 at 1/500 (0.99 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control : no staining on human liver. The primary antibody was incubated 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 Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- WB
Lab
Western blot - Anti-SLC34A2 antibody [EPR30528-645] (AB325747)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
This antibody does not cross-react with overexpressed human SLC34A1 or SLC34A3 by western blot.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) (1 : 200000) (36KDa); Anti-6X His tag® antibody [EPR20547] - ChIP Grade (ab213204) (1 : 5000) (75-100KDa).
All lanes:
Western blot - Anti-SLC34A2 antibody [EPR30528-645] (ab325747) at 1/1000 dilution
Lane 1:
293T (human embryonic kidney epithelial cell) cells transfected with an empty vector containing a myc-His-tag® whole cell lysate at 5 µg
Lane 2:
293T cells transfected with human SLC34A2 expression vector containing a myc-His-tag® whole cell lysate at 5 µg
Lane 3:
293T cells transfected with human SLC34A1 expression vector containing a myc-His-tag® whole cell lysate at 5 µg
Lane 4:
293T cells transfected with human SLC34A3 expression vector containing a myc-His-tag® whole cell lysate at 5 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 75-150 kDa,36 kDa,75-100 kDa
false
Exposure time: 15s
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
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
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Storage information
Product protocols
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Target data
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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