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AB83353

Recombinant HIV1 tat protein

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(4 Publications)

Recombinant HIV1 tat protein is a Full Length protein, in the 1 to 101 aa range with >90% purity and suitable for western blot, SDS-PAGE, and Blocking assays. The predicted molecular weight of ab83353 protein is 20.1 kDa.

- Recombinant HIV-1 Tat Clade C
- Save time and ensure accurate results- use our HIV1 tat protein as a control
- Available in different sizes to fit your experimental needs

Key facts

Purity

>90% SDS-PAGE

Expression system

Escherichia coli

Tags

Tag free

Applications

BL, WB, SDS-PAGE

applications

Biologically active

No

Animal free

No

Carrier free

No

Reconstitution

Reconstitute in PBS

Storage buffer

Constituents: 0.1% Glycerol (glycerin, glycerine)

storage-buffer

Reactivity data

{ "title": "Reactivity Data", "filters": { "stats": ["", "Reactivity", "Dilution Info", "Notes"] }, "values": { "SDS-PAGE": { "reactivity":"TESTED_AND_REACTS", "dilution-info":"", "notes":"<p></p>" }, "WB": { "reactivity":"TESTED_AND_REACTS", "dilution-info":"", "notes":"<p></p>" }, "BL": { "reactivity":"TESTED_AND_REACTS", "dilution-info":"", "notes":"<p></p>" } } }

Product details

Ensure the validity of your result using our recombinant HIV1 tat protein ab83353 as a positive control in western blot and SDS-PAGE. The HIV-1 TAT protein Clade C is a molecule of 101 amino acids encoded by two exons. ab83353 reacts with anti-Tat antibodies from human, monkey, rabbit and mouse serum.

This is a biologically non-active protein estimated by Up-Take and Rescue assays (positive to uptake assay but negative to rescue assay).


Check out our protein gel staining guide for SDS-PAGE here

Check out of western blot protocol for more information here

Sequence info

[{"sequence":"","proteinLength":"Full Length","predictedMolecularWeight":null,"actualMolecularWeight":null,"aminoAcidEnd":101,"aminoAcidStart":1,"nature":"Recombinant","expressionSystem":"Escherichia coli","accessionNumber":null,"tags":[]}]

Properties and storage information

Shipped at conditions
Ambient - Cannot Ship with Ice
Appropriate short-term storage conditions
-20°C
Appropriate long-term storage conditions
-20°C
Storage information
Avoid freeze / thaw cycle
False

Supplementary information

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

The HIV-1 Tat protein also known as HIV Tat or simply Tat is an important regulatory protein of the Human Immunodeficiency Virus type 1 (HIV-1). It has a mass of approximately 14 to 16 kDa and is important for viral replication. This protein is expressed early in the HIV-1 infection cycle and is localized mainly in the nucleus of infected T-cells. HIV-1 Tat is known for its ability to transactivate the HIV-1 long terminal repeat (LTR) promoter which significantly enhances the production of viral RNA.
Biological function summary

The HIV-1 Tat protein plays an important role in the replication and transcription processes of the HIV-1 virus. It is part of a complex that interacts with other host cellular factors to improve the efficiency of the HIV-1 transcription from the provirus. This interaction is essential for the elongation phase of transcription which results in increased viral gene expression and successful replication of the virus inside host cells.

Pathways

The involvement of the HIV-1 Tat protein extends to interfering with several important biological pathways. It influences the NF-kB pathway which is critical for immune response regulation and interacts with the Cyclin T1 as part of the P-TEFb complex. This interaction is important for the transcriptional activation of the HIV LTR. By affecting the NF-kB pathway Tat protein indirectly modulates inflammatory responses which can lead to altered immune system functions.

HIV-1 Tat protein's primary significance lies in the progression and pathology of HIV/AIDS. Its interactions with host cellular proteins such as CDK9 (a component of P-TEFb) are critical for viral persistence and pathogenesis. Additionally Tat has been implicated in neurological disorders associated with HIV-1 infection often referred to as HIV-associated neurocognitive disorders (HAND). Its influence on the central nervous system arises from its ability to exit infected cells and exert neurotoxic effects in neighboring uninfected neural cells.

Specifications

Form

Lyophilized

General info

Product protocols

Publications (4)

Recent publications for all applications. Explore the full list and refine your search

International journal of molecular sciences 24: PubMed36613717

2022

HIV-Tat Exacerbates the Actions of Atazanavir, Efavirenz, and Ritonavir on Cardiac Ryanodine Receptor (RyR2).

Applications

Unspecified application

Species

Unspecified reactive species

Fadhel A Alomar,Chengju Tian,Sean R Bidasee,Zachary L Venn,Evan Schroder,Nicholas Y Palermo,Mohammad AlShabeeb,Benson J Edagwa,Jason J Payne,Keshore R Bidasee

Science advances 7:eabi5751 PubMed34890234

2021

The nuclear transcription factor, TAF7, is a cytoplasmic regulator of protein synthesis.

Applications

Unspecified application

Species

Unspecified reactive species

Dan Cheng,Kevin Semmens,Elizabeth McManus,Qingrong Chen,Daoud Meerzaman,Xiantao Wang,Markus Hafner,Brian A Lewis,Hidehisa Takahashi,Ballachanda N Devaiah,Anne Gegonne,Dinah S Singer

Journal of neuroinflammation 16:71 PubMed30947729

2019

HIV-1 Tat enhances purinergic P2Y4 receptor signaling to mediate inflammatory cytokine production and neuronal damage via PI3K/Akt and ERK MAPK pathways.

Applications

Unspecified application

Species

Unspecified reactive species

Feng Zhou,Xiaomei Liu,Lin Gao,Xinxin Zhou,Qianwen Cao,Liping Niu,Jing Wang,Dongjiao Zuo,Xiangyang Li,Ying Yang,Minmin Hu,Yinghua Yu,Renxian Tang,Bong Ho Lee,Byoung Wook Choi,Yugang Wang,Yoshihiro Izumiya,Min Xue,Kuiyang Zheng,Dianshuai Gao

BMC immunology 13:15 PubMed22471703

2012

The Tat protein of human immunodeficiency virus-1 enhances hepatitis C virus replication through interferon gamma-inducible protein-10.

Applications

Unspecified application

Species

Unspecified reactive species

Jing Qu,Qi Zhang,Youxing Li,Weiyong Liu,Lvxiao Chen,Ying Zhu,Jianguo Wu
View all publications

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