Anti-SLC1A5/ASCT2 抗体 [CAL33] - BSA and Azide free
Anti-SLC1A5/ASCT2 antibody [CAL33] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- KO Validated
- Recombinant
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(2 Publications)
Rabbit Recombinant Monoclonal SLC1A5/ASCT2 antibody. Carrier free. Suitable for IP, WB, ICC/IF, Flow Cyt (Intra), IHC-P and reacts with Human samples. Cited in 2 publications.
別名を表示する
ASCT2, M7V1, RDR, RDRC, SLC1A5, Neutral amino acid transporter B(0), ATB(0), Baboon M7 virus receptor, RD114/simian type D retrovirus receptor, Sodium-dependent neutral amino acid transporter type 2, Solute carrier family 1 member 5
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-SLC1A5/ASCT2 antibody [CAL33] - BSA and Azide free (AB251591)
Immunofluorescent analysis of 100% methanol fixed Jurkat (human T cell leukemia T lymphocyte) cells labeling SLC1A5/ASCT2 with ab237704 at 1/50 dilution, followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077) secondary antibody at 1/1000 dilution (green). Confocal image showing membranous staining in Jurkat cells. The nuclear counter stain is DAPI (blue).
Counterstained with ab195889 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594) at a 1/200 dilution (red). The negative control is the secondary antibody only.
This data was developed using the same antibody clone in a different buffer formulation containing PBS and sodium azide (ab237704).
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SLC1A5/ASCT2 antibody [CAL33] - BSA and Azide free (AB251591)
Formalin-fixed, paraffin-embedded human colon carcinoma tissue stained for SLC1A5/ASCT2 using ab237704 at 0.5 μg/ml in immunohistochemical analysis.
This data was developed using the same antibody clone in a different buffer formulation containing PBS and sodium azide (ab237704).
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SLC1A5/ASCT2 antibody [CAL33] - BSA and Azide free (AB251591)
Immunohistochemical analysis of paraffin-embedded human lung carcinoma tissue labeling SLC1A5/ASCT2 with ab237704 at 1/1600 dilution, followed by a ready to use Goat Anti-Rabbit IgG H&L (HRP). Mainly membranous staining on the human lung carcinoma is observed. The section was incubated with ab237704 for 15 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with hematoxylin. Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is a ready to use Goat Anti-Rabbit IgG H&L (HRP). Perform heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS and sodium azide (ab237704).
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SLC1A5/ASCT2 antibody [CAL33] - BSA and Azide free (AB251591)
Immunohistochemical analysis of paraffin-embedded human colon carcinoma tissue labeling SLC1A5/ASCT2 with ab237704 at 1/1600 dilution, followed by a ready to use Goat Anti-Rabbit IgG H&L (HRP). Mainly membranous staining on the human colon carcinoma is observed. The section was incubated with ab237704 for 15 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with hematoxylin. Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is a ready to use Goat Anti-Rabbit IgG H&L (HRP). Perform heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS and sodium azide (ab237704).
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-SLC1A5/ASCT2 antibody [CAL33] - BSA and Azide free (AB251591)
Immunofluorescent analysis of 100% methanol fixed HeLa (human cervix adenocarcinoma epithelial cell) cells labeling SLC1A5/ASCT2 with ab237704 at 1/50 dilution, followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077) secondary antibody at 1/1000 dilution (green). Confocal image showing membranous staining in HeLa cells. The nuclear counter stain is DAPI (blue).
Counterstained with ab195889 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594) at a 1/200 dilution (red). The negative control is the secondary antibody only.
This data was developed using the same antibody clone in a different buffer formulation containing PBS and sodium azide (ab237704).
- Flow Cyt (Intra)
Lab
Flow Cytometry (Intracellular) - Anti-SLC1A5/ASCT2 antibody [CAL33] - BSA and Azide free (AB251591)
Intracellular flow cytometric analysis of 4% paraformaldehyde-fixed, 90% methanol permeabilized Jurkat (human T cell leukemia T lymphocyte) cell line labeling SLC1A5/ASCT2 with ab237704 at 1/40 (red) compared with a Rabbit monoclonal IgG (ab172730) (black) and an unlabeled control (cells without incubation with primary antibody and secondary antibody) (blue). Goat anti rabbit IgG (Alexa Fluor® 488, ab150077), at 1/2000 dilution was used as the secondary antibody.
This data was developed using the same antibody clone in a different buffer formulation containing PBS and sodium azide (ab237704).
- Flow Cyt (Intra)
Lab
Flow Cytometry (Intracellular) - Anti-SLC1A5/ASCT2 antibody [CAL33] - BSA and Azide free (AB251591)
Intracellular flow cytometric analysis of 4% paraformaldehyde-fixed, 90% methanol permeabilized HeLa (human cervix adenocarcinoma epithelial cell) cell line labeling SLC1A5/ASCT2 with ab237704 at 1/400 (red) compared with a Rabbit monoclonal IgG (ab172730) (black) and an unlabeled control (cells without incubation with primary antibody and secondary antibody) (blue). Goat anti rabbit IgG (Alexa Fluor® 488, ab150077), at 1/2000 dilution was used as the secondary antibody.
This data was developed using the same antibody clone in a different buffer formulation containing PBS and sodium azide (ab237704).
- IP
Lab
Immunoprecipitation - Anti-SLC1A5/ASCT2 antibody [CAL33] - BSA and Azide free (AB251591)
SLC1A5/ASCT2 was immunoprecipitated from 0.35 mg Jurkat (human T cell leukemia T lymphocyte) whole cell lysate with ab237704 at 1/30 dilution. Western blot was performed from the immunoprecipitate using ab237704 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP) (ab131366), was used at 1/5000 dilution.
Lane 1 : Jurkat whole cell lysate 10 μg (Input).
Lane 2 : ab237704 IP in Jurkat whole cell lysate.
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab237704 in Jurkat whole cell lysate.
Blocking/Dilution buffer : 5% NFDM/TBST.
ASCT2 (SLC1A5) can form dimers or trimers based on literature. (PMID : 23756778).
This data was developed using the same antibody clone in a different buffer formulation containing PBS and sodium azide (ab237704).
All lanes:
Immunoprecipitation - Anti-SLC1A5/ASCT2 antibody [CAL33] (<a href='/products/primary-antibodies/slc1a5-asct2-antibody-cal33-ab237704'>ab237704</a>) at 1/30 dilution
Predicted band size: 56 kDa
false
Exposure time: 3s
- IP
Lab
Immunoprecipitation - Anti-SLC1A5/ASCT2 antibody [CAL33] - BSA and Azide free (AB251591)
SLC1A5/ASCT2 was immunoprecipitated from 0.35 mg HeLa (human cervix adenocarcinoma epithelial cell) whole cell lysate with ab237704 at 1/30 dilution. Western blot was performed from the immunoprecipitate using ab237704 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP) (ab131366), was used at 1/5000 dilution.
Lane 1 : HeLa whole cell lysate 10 μg (Input).
Lane 2 : ab237704 IP in HeLa whole cell lysate.
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab237704 in HeLa whole cell lysate.
Blocking/Dilution buffer : 5% NFDM/TBST.
ASCT2 (SLC1A5) can form dimers or trimers based on literature. (PMID : 23756778).
This data was developed using the same antibody clone in a different buffer formulation containing PBS and sodium azide (ab237704).
All lanes:
Immunoprecipitation - Anti-SLC1A5/ASCT2 antibody [CAL33] (<a href='/products/primary-antibodies/slc1a5-asct2-antibody-cal33-ab237704'>ab237704</a>) at 1/30 dilution
Predicted band size: 56 kDa
false
Exposure time: 1s
- WB
Lab
Western blot - Anti-SLC1A5/ASCT2 antibody [CAL33] - BSA and Azide free (AB251591)
This data was developed using the same antibody clone in a different buffer formulation containing PBS and sodium azide (ab237704).
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Exposure time :
Lane 1 : 80 seconds
Lane 2 : 40 seconds
An extra band around 50 kDa might be observed. We are not sure how to define it.
All lanes:
Western blot - Anti-SLC1A5/ASCT2 antibody [CAL33] (<a href='/products/primary-antibodies/slc1a5-asct2-antibody-cal33-ab237704'>ab237704</a>) at 1/1000 dilution
Lane 1:
HeLa (human cervix adenocarcinoma epithelial cell) whole lysate at 15 µg
Lane 2:
293T (Human embryonic kidney epithelial cell) whole lysate at 15 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Observed band size: 75 kDa
false
関連する標識済み抗体及び組成の異なる製品 (1)
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Anti-SLC1A5/ASCT2 antibody [CAL33]
Reactivity data
製品の詳細
ab251591 is the carrier-free version of ab237704.
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.
出荷温度及び保存条件
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精製方法
精製に関する特記事項
バッファー組成
出荷温度
短期保存温度
長期保存温度
保管に関する情報
補足情報
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
The SLC1A5 protein contributes to cellular processes by facilitating the uptake of neutral amino acids. ASCT2 operates as a part of a complex of transporters that ensure the supply of critical nutrients within cells impacting metabolic processes like protein synthesis and cell growth. Its function supports the dynamic needs of rapidly growing tissues and is especially active in conditions demanding high amino acid turnover.
Pathways
The activity of SLC1A5/ASCT2 is important in amino acid transport pathways particularly influencing the mTOR signaling which plays a significant role in cell growth and metabolic regulation. SLC1A5/ASCT2 interaction with proteins like LAT1 strengthens its involvement in these pathways. These interactions outline a network of nutrient sensing and metabolic control important for cellular proliferation and homeostasis.
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文献 (2)
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Drug design, development and therapy 18:3157-3173 PubMed39071813
2024
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Cancer cell 40:1423-1439.e11 PubMed36240778
2022
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