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AB271302

Anti-TVA antibody [PICA187E] - BSA and Azide free

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Rat Recombinant Monoclonal ENV antibody. Carrier free. Suitable for WB, ICC/IF, IHC-P, Flow Cyt (Intra) and reacts with Transfected cell line - Bird samples.

View Alternative Names

Subgroup A Rous sarcoma virus receptor pg950, Low density lipoprotein receptor-related protein, Tva

7 Images
Immunocytochemistry/ Immunofluorescence - Anti-TVA antibody [PICA187E] - BSA and Azide free (AB271302)
  • ICC/IF

Lab

Immunocytochemistry/ Immunofluorescence - Anti-TVA antibody [PICA187E] - BSA and Azide free (AB271302)

This data was developed using ab271292 the same antibody clone in a different buffer formulation.

Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized HEK-293T (human embryonic kidney) cells transfected with myc-tagged TVA expression vector labelling TVA with ab271292 at 1/50 (21.96 μg/ml) dilution, followed by ab150157 Goat Anti-rat IgG H&L (Alexa Fluor® 488) antibody at 1/1000 dilution (Green). Confocal image showing cytoplasmic staining in HEK-293T cells transfected with myc-tagged TVA expression vector. Myc-Tag mouse mAb (Alexa Fluor® 647) was used as a counterstain at 1/200 dilution (Red). The nuclear counterstain was DAPI (Blue).

Secondary antibody control : Used PBS instead of ab271292, followed by ab150157 Goat Anti-rat IgG H&L (Alexa Fluor® 488) antibody at 1/1000 dilution.

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TVA antibody [PICA187E] - BSA and Azide free (AB271302)
  • IHC-P

Lab

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TVA antibody [PICA187E] - BSA and Azide free (AB271302)

This data was developed using ab271292 the same antibody clone in a different buffer formulation.

Immunohistochemical analysis of paraffin-embedded human cerebrum tissue labeling TVA with ab271292 at 1/100 (10.98 μg/ml) dilution followed by a ready to use Goat Anti-rat IgG H&L (HRP polymer) (ab214882). Negative control : No staining on human cerebrum. The section was incubated with ab271292 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 Goat Anti-rat IgG H&L (HRP polymer) (ab214882).

Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.

Flow Cytometry (Intracellular) - Anti-TVA antibody [PICA187E] - BSA and Azide free (AB271302)
  • Flow Cyt (Intra)

Lab

Flow Cytometry (Intracellular) - Anti-TVA antibody [PICA187E] - BSA and Azide free (AB271302)

This data was developed using ab271292 the same antibody clone in a different buffer formulation.

Intracellular flow cytometric analysis of 4% paraformaldehyde-fixed, 90% methanol-permeabilized HEH-293T (human embryonic kidney epithelial cell) (transfected with myc tagged TVA construct) cells labelling TVA with ab271292 at 1/1000 dilution (0.1μg) (Right panel) compared with a rat monoclonal IgG isotype control (Left panel). Goat F (ab)2 Anti-Rat IgG Fc (Alexa Fluor®488, ab150161)was used as the secondary antibody at a 1/2000 dilution.

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TVA antibody [PICA187E] - BSA and Azide free (AB271302)
  • IHC-P

Lab

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TVA antibody [PICA187E] - BSA and Azide free (AB271302)

This data was developed using ab271292 the same antibody clone in a different buffer formulation.

Immunohistochemical analysis of paraffin-embedded (Panel A) HEK-293T transfected with a TVA construct and (Panel B) HEK-293T transfected with empty plasmid, labeling TVA with ab271292 at 1/100 (10.98 μg/ml) dilution followed by a ready to use Goat Anti-rat IgG H&L (HRP polymer) (ab214882). Positive staining on (Panel A) HEK-293T transfected with a TVA construct, no staining on (Panel B) HEK-293T transfected with empty plasmid. The section was incubated with ab271292 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 Goat Anti-rat IgG H&L (HRP polymer) (ab214882).

Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TVA antibody [PICA187E] - BSA and Azide free (AB271302)
  • IHC-P

Lab

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TVA antibody [PICA187E] - BSA and Azide free (AB271302)

This data was developed using ab271292 the same antibody clone in a different buffer formulation.

Immunohistochemical analysis of paraffin-embedded mouse cerebrum tissue labeling TVA with ab271292 at 1/100 (10.98 μg/ml) dilution followed by a ready to use Goat Anti-rat IgG H&L (HRP polymer) (ab214882). Negative control : No staining on mouse cerebrum. The section was incubated with ab271292 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 Goat Anti-rat IgG H&L (HRP polymer) (ab214882).

Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TVA antibody [PICA187E] - BSA and Azide free (AB271302)
  • IHC-P

Lab

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TVA antibody [PICA187E] - BSA and Azide free (AB271302)

This data was developed using ab271292 the same antibody clone in a different buffer formulation.

Immunohistochemical analysis of paraffin-embedded rat cerebrum tissue labeling TVA with ab271292 at 1/100 (10.98 μg/ml) dilution followed by a ready to use Goat Anti-rat IgG H&L (HRP polymer) (ab214882). Negative control : No staining on rat cerebrum. The section was incubated with ab271292 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 Goat Anti-rat IgG H&L (HRP polymer) (ab214882).

Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.

Western blot - Anti-TVA antibody [PICA187E] - BSA and Azide free (AB271302)
  • WB

Lab

Western blot - Anti-TVA antibody [PICA187E] - BSA and Azide free (AB271302)

This data was developed using ab271292 the same antibody clone in a different buffer formulation.

Blocking/Dilution buffer : 5% NFDM/TBST.

All lanes:

Western blot - Anti-TVA antibody [PICA187E] (<a href='/en-us/products/primary-antibodies/tva-antibody-pica187e-ab271292'>ab271292</a>) at 1/5000 dilution

Lane 1:

HEK-293T (human embryonic kidney) transfected with an empty vector (vector control), containing a myc-His-tag®, whole cell lysate at 10 µg

Lane 2:

HEK-293T transfected with TVA expression vector containing a myc-His-tag®, whole cell lysate at 10 µg

Secondary

All lanes:

Western blot - Goat Anti-Rat IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rat-igg-h-l-hrp-ab205720'>ab205720</a>) at 1/50000 dilution

Observed band size: 25-37 kDa

false

Exposure time: 10s

Key facts

Host species

Rat

Clonality

Monoclonal

Clone number

PICA187E

Isotype

IgG2b

Carrier free

Yes

Reacts with

Bird

Applications

ICC/IF, IHC-P, Flow Cyt (Intra), WB

applications

Immunogen

The exact immunogen used to generate this antibody is proprietary information.

Reactivity data

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Product details

ab271302 is the carrier-free version of ab271292.

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.

Want a custom formulation?
This antibody clone is manufactured by Abcam. If you require a custom buffer formulation or conjugation for your experiments, please contact orders@abcam.com

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.

Properties and storage information

Form
Liquid
Purification technique
Affinity purification Protein A
Storage buffer
Constituents: PBS
Shipped at conditions
Blue Ice
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
+4°C
Storage information
Do Not Freeze

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

The Tumor Virus A Receptor (TVA) often referred to as Tva or LDLR family member 1 (LDLR1) is a protein that acts as a receptor for specific avian sarcoma and leukosis viruses (ASLV) subgroup A. It has a molecular mass of approximately 47 kDa. TVA is expressed on the surface of cells in various tissues playing a role in viral entry. It belongs to the low-density lipoprotein receptor (LDLR) family which is involved in endocytosis and ligand binding processes.
Biological function summary

TVA acts as part of the viral entry complex facilitating the binding and internalization of certain retroviruses. Through its function as a receptor TVA allows the virus to attach to and penetrate host cells initiating infection. The protein’s role in viral entry makes it important for viral lifecycle progression. TVA does not function in isolation but often works in tandem with other receptors to mediate efficient viral uptake into the host cell.

Pathways

TVA participates in the endocytosis pathway which is integral for the uptake of viruses into cells. This pathway includes other proteins such as clathrin and dynamin which play roles in vesicle formation and membrane scission. TVA's interaction with these components facilitates the internalization and trafficking of viral particles within the host cell aiding in the infection process. The protein is also related to signal transduction pathways that might be hijacked by viruses to sustain their replication inside host cells.

The role of TVA in viral infections positions it as a critical factor in understanding certain leukemias and sarcomas caused by ASLV. The infection process mediated by TVA can lead to cellular transformation and tumorigenesis particularly in avian species. While direct associations with human diseases have not been extensively documented studying TVA's interaction with viral glycoproteins provides insight into similar mechanisms in other retroviral infections including those involving related receptors like LDLR.

Product protocols

For this product, it's our understanding that no specific protocols are required. You can visit:

Target data

Responsible for susceptibility to the retrovirus subgroup A Rous sarcoma virus.
See full target information RSVR_COTJA

Product promise

We are committed to supporting your work with high-quality reagents, and we're here for you every step of the way. In the unlikely event that one of our products does not perform as expected, you're protected by our Product Promise.
For full details, please see our Terms & Conditions

Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.

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