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ATG5 HumanDescription:
Autophagy Related 5 Human Recombinant
Autophagy protein 5, APG5-like, Apoptosis-specific protein, ATG5, ASP, APG5, APG5L, hAPG5.
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PRO-454Price :
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Shipped with Ice Packs
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ATG4B HumanDescription:
ATG4 Autophagy Related 4 Homolog B Human Recombinant
Cysteine protease ATG4B, AUT-like 1 cysteine endopeptidasem, Autophagin-1, Autophagy-related cysteine endopeptidase 1, Autophagy-related protein 4 homolog B, hAPG4B, ATG4B, APG4B, AUTL1, KIAA0943.
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PRO-1048Price :
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ATG3 HumanDescription:
Autophagy Related 3 Human Recombinant
APG3, APG3-LIKE, APG3L, PC3-96, Ubiquitin-like-conjugating enzyme ATG3, Autophagy-related protein 3, hApg3, PC3-96, ATG3.
Product # :
PRO-1987Price :
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ATG10 HumanDescription:
Autophagy Related 10 Human Recombinant
Autophagy Related Protein 10, ATG10 Autophagy Related 10 Homolog (S. Cerevisiae), Ubiquitin-Like-Conjugating Enzyme ATG10, APG10 Autophagy 10-Like (S. Cerevisiae), APG10-Like, APG10L, Pp12616, DKFZP586I0418, FLJ13954, EC 6.3.2.-.
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PRO-1234Price :
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About ATG / Autophagy Related:
Autophagy related protein, otherwise known as ATG, is involved in the regulation of dsDNA-induced innate immune responses, and is therefore a very important aspect to physiological immunity and wellbeing in all forms of life.
ATG Function & Structure
It has been shown that atg9a regulates membrane trafficking involved in the movement of STING and dsDNA-induced production of type I IFNs. In general, these autophagosomes target and subsequently take over bacteria-containing vacuoles in a manner which is recognized as STING-dependent. As such, they also mediate the auto lysosomal degradation of invading bacteria.
Similarly, these autophagosomes also target and engulf ubiquitinated ASC, which in turn allows them to mediate auto lysosomal degradation of the AIM2-inflammasome, which is a key way to suppress the dsDNA-induced production of any inflammatory cytokines. As you might imagine, it is therefore an important part of fighting for immunity in many physiological systems.
Autophagy Related Uses
When we look at how these might be used therapeutically, the potential looks very strong. One good example is with DNA vaccination, a method for protecting a given organism against microbial infection and a range of cancers, using the genetic injection of dsDNA encoding, a protein antigen can then effectively stimulate the humoral and cellular immune responses. At the same time, such DNA vaccination of this kind causes an activation of the STING–TBK1 signaling axis, which in turn induces acquired immune responses. The result is the generation of antigen-specific T cells and the further production of antigen-specific antibodies.