Recombinant Mouse Protein FADD (Fadd)

Code CSB-YP730727MO
Size Pls inquire
Source Yeast
Have Questions? Leave a Message or Start an on-line Chat
Code CSB-EP730727MO
Size Pls inquire
Source E.coli
Have Questions? Leave a Message or Start an on-line Chat
Code CSB-EP730727MO-B
Size Pls inquire
Source E.coli
Conjugate Avi-tag Biotinylated
E. coli biotin ligase (BirA) is highly specific in covalently attaching biotin to the 15 amino acid AviTag peptide. This recombinant protein was biotinylated in vivo by AviTag-BirA technology, which method is BriA catalyzes amide linkage between the biotin and the specific lysine of the AviTag.
Have Questions? Leave a Message or Start an on-line Chat
Code CSB-BP730727MO
Size Pls inquire
Source Baculovirus
Have Questions? Leave a Message or Start an on-line Chat
Code CSB-MP730727MO
Size Pls inquire
Source Mammalian cell
Have Questions? Leave a Message or Start an on-line Chat

Product Details

>85% (SDS-PAGE)
Target Names
Uniprot No.
Alternative Names
Fadd; Mort1FAS-associated death domain protein; FAS-associating death domain-containing protein; Mediator of receptor induced toxicity; Protein FADD
Mus musculus (Mouse)
Expression Region
Target Protein Sequence
Protein Length
full length protein
Tag Info
Tag type will be determined during the manufacturing process.
The tag type will be determined during production process. If you have specified tag type, please tell us and we will develop the specified tag preferentially.
Lyophilized powder
Note: We will preferentially ship the format that we have in stock, however, if you have any special requirement for the format, please remark your requirement when placing the order, we will prepare according to your demand.
Buffer before Lyophilization
Tris/PBS-based buffer, 6% Trehalose, pH 8.0
We recommend that this vial be briefly centrifuged prior to opening to bring the contents to the bottom. Please reconstitute protein in deionized sterile water to a concentration of 0.1-1.0 mg/mL.We recommend to add 5-50% of glycerol (final concentration) and aliquot for long-term storage at -20℃/-80℃. Our default final concentration of glycerol is 50%. Customers could use it as reference.
Troubleshooting and FAQs
Storage Condition
Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. Avoid repeated freeze-thaw cycles.
Shelf Life
The shelf life is related to many factors, storage state, buffer ingredients, storage temperature and the stability of the protein itself.
Generally, the shelf life of liquid form is 6 months at -20°C/-80°C. The shelf life of lyophilized form is 12 months at -20°C/-80°C.
Lead Time
Delivery time may differ from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
Note: All of our proteins are default shipped with normal blue ice packs, if you request to ship with dry ice, please communicate with us in advance and extra fees will be charged.
Repeated freezing and thawing is not recommended. Store working aliquots at 4°C for up to one week.
Please contact us to get it.

Customer Reviews and Q&A

 Customer Reviews

There are currently no reviews for this product.

Submit a Review here

Target Background

Apoptotic adaptor molecule that recruits caspase-8 or caspase-10 to the activated Fas (CD95) or TNFR-1 receptors. The resulting aggregate called the death-inducing signaling complex (DISC) performs caspase-8 proteolytic activation. Active caspase-8 initiates the subsequent cascade of caspases mediating apoptosis. Involved in interferon-mediated antiviral immune response, playing a role in the positive regulation of interferon signaling.
Gene References into Functions
  1. results show that N-FADD is a more potent apoptotic inducer and VNP20009-mediated targeted expression of N-FADD provides a possible cancer gene therapeutic approach for the treatment of melanoma. PMID: 27767039
  2. these results demonstrated that RIPK3-mediated signaling in Tie-2 expressing cells was responsible for the embryonic lethality of Fadd-/- with cardiac failure. PMID: 27584790
  3. The study provides genetic evidence that different RIP1 kinase inactive mutations have distinct impacts on the embryogenesis of Fadd-deficient mice. PMID: 28574501
  4. Our findings reveal that MLKL and FADD play critical roles in preventing lymphoproliferative disease and activating the NLRP3 inflammasome PMID: 27498868
  5. miR-7a was a necessary mediator in FADD-regulated FAK expression. In contrast to its classical apoptotic role, FADD interference could reduce the rate of cell migration, which could be rescued by inhibiting miR-7a expression. PMID: 27286445
  6. In macrophages, ultraviolet radiation induced association of MyD88 with FADD and migration of FADD to the cell membrane PMID: 27676214
  7. The authors conclude that FADD is a master regulator of glucose and fat metabolism. PMID: 27357657
  8. Mice deficient in RIPK3 or doubly deficient in MLKL and FADD, but not MLKL alone, are more susceptible to influenza A virus than their wild-type counterparts, revealing an important role for RIPK3-mediated apoptosis in antiviral immunity. PMID: 27321907
  9. Wild-type cells can execute apoptosis via both, the mitochondrial and the receptor-mediated pathway whereas FADD-deficient cells can only activate the intrinsic pathway. There is a difference in UVC radiation response between two cell lines indicating the role of FADD in the selection of cell death modality. PMID: 27258329
  10. This study reveals an essential role of SUMOylated FADD in Drp1- and caspase-10-dependent necrosis. PMID: 27799292
  11. Deletion of FADD in macrophages and granulocytes results in RIP3- and MyD88-dependent systemic inflammation. PMID: 25874713
  12. A constitutively phosphoryl-mimicking mutation of Fas-associated death domain (FADD-D) enhances Notch-1 signaling and compromises Wnt signaling in both cultured myoblasts and regenerating muscles. PMID: 26303234
  13. Beta amyloid-induced upregulation of death receptor 6 accelerates the toxic effect of N-terminal fragment of amyloid precursor protein PMID: 25150572
  14. Phosphorylation of FADD by the kinase CK1alpha promotes KRASG12D-induced lung cancer. PMID: 25628462
  15. This study evaluated the role of FADD in pancreatic islets and insulin secretion. PMID: 25641109
  16. depletion of alphaNAC in multiple types of cancer cells induce typical apoptotic cell death. This anti-apoptotic function is mediated by the FADD/c-Jun N-terminal kinase pathway. PMID: 24901053
  17. These data suggest that as a death receptor, FADD is also required for cell survival in beta-selection as a regulator of Notch1 expression. PMID: 24901044
  18. using T-cell specific deletion mice, we observed that FADD deficiency in thymocytes led to increased apoptosis and reduced cell numbers, which may be attributed to the reduction of Glut1 expression and correspondingly decreased glucose uptake PMID: 25078620
  19. FADD deficiency protects against myocardial ischemia/reperfusion injury in a heart failure mouse model. PMID: 24058479
  20. glycogen synthesis, glycolysis, and gluconeogenesis were dysregulated because of FADD phosphorylation, both in MEFs and liver tissue of the mice bearing phosphorylation-mimicking mutation form of FADD. PMID: 23828893
  21. FADD regulates the fate determination of cycling satellite cells. PMID: 24375410
  22. p45 forms a complex with FADD and diminishes Fas-FADD mediated death signaling. PMID: 23935974
  23. Used proteomics and bioinformatic analysis to study proteins differentially expressed in three cell lines containing FADD and its mutant, FADD-A and FADD-D. PMID: 23744592
  24. Impaired mitochondrial function and proteolysis may play pivotal roles in the dysfunction associated with FADD deficiency-induced disorders, probably including embryonic lethality. PMID: 23689606
  25. FADD Protects Cells from IFN-gamma-Activated Necrosis by Preventing Formation of the RIP1-RIP3 Necrosome. PMID: 23898178
  26. Fas (TNF receptor superfamily member CD95) activates interleukin (IL)-1beta and IL-18 in a caspase-8- and Fas-associated death domain (FADD) protein-dependent and receptor-interacting protein (Rip)3-independent pathway. PMID: 23144495
  27. show that epidermal keratinocyte-restricted deficiency of the adaptor protein FADD (FADD(E-KO)) induced severe inflammatory skin lesions in mice PMID: 22000287
  28. RIPK3 and FADD have opposing and complementary roles in promoting T-cell clonal expansion and homeostasis. PMID: 21876153
  29. tumor necrosis factor alpha-induced necroptosis requires the adaptor proteins FADD and NEMO. PMID: 21746883
  30. mechanisms preventing RIP3-mediated epithelial cell death are critical for maintenance of intestinal homeostasis and indicate that programmed necrosis of intestinal epithelial cells might be implicated in the pathogenesis of inflammatory bowel disease PMID: 21804564
  31. data demonstrate an unexpected cell-type-specific interplay between FADD and RIP1, which is critical for the regulation of apoptosis and necrosis during embryogenesis and lymphocyte function PMID: 21368761
  32. specific polymorphisms at Fas, FasL and Fadd genes that differentiate mouse strains exhibiting extreme differences in susceptibility to gamma radiation-induced T-cell lymphomas. PMID: 20889682
  33. FADD is critical for ODC apoptosis and the development of autoimmune demyelinating disease. PMID: 21068410
  34. molecular studies led to the discovery of a previously unappreciated HIF-1 binding site in the FADD promoter, which controls repression of FADD during hypoxia. PMID: 20943999
  35. FADD constitutes a mechanism to keep TCR-induced programmed necrotic signaling in check during early phases of T-cell clonal expansion. PMID: 20615958
  36. Importance in signaling in serum deprivation and hypoxia-induced cardiomyocyte apoptosis PMID: 12063258
  37. inhibition of FADD function blocks proliferation but not MAP kinase-activation and interleukin-2-production during primary stimulation of T cells PMID: 12115619
  38. MORT1/FADD is indispensable for Fas and TNF-mediated hepatic injury PMID: 12500197
  39. FADD acquired a domain during evolution, rendering it a "proliferation-apoptosis coupler" that balances cell proliferation and apoptosis. PMID: 12705854
  40. Loss of this protein's expression results in a biased Fas-signaling pathway and correlates with the development of tumoral status in thyroid follicular cells. PMID: 12743602
  41. In a highly regulated fashion, FADD can transduce either a signal for survival or one that leads directly to apoptosis; the balance between these opposing outcomes is crucial to adaptive immunity. PMID: 12817005
  42. RIP, TRAF2, and FADD are crucial in mediating ROS accumulation in TNF-induced necrotic cell death PMID: 14701813
  43. Modifications and intracellular trafficking of Mort1 after T-lymphocyte activation was studied. PMID: 15017386
  44. binding of Fas-associated death domain (FADD) to the tumor necrosis factor-related apoptosis-inducing ligand receptor DR5 is regulated by the death effector domain of FADD PMID: 15173180
  45. FasL induces NF-kappaB activation and IL-8 production by a novel mechanism, distinct from that of TNF-alpha and FADD had a dominant-negative effect on the FasL-induced NF-{kappa}B activation. PMID: 15337758
  46. Data suggest that the loss of FADD/caspase-8 function during development and/or in mature T cells selectively impacts on some but not other pathways of T-cell activation and maturation. PMID: 15376191
  47. mammalian cells lacking the death-domain-containing protein FADD are defective in intracellular dsRNA-activated gene expression, including production of type I (alpha/beta) interferons, and are thus very susceptible to viral infection PMID: 15549108
  48. A site is identified in the death domain of FADD that is essential for signal-specific binding to Fas and TRADD and for mediating apoptosis. PMID: 16009710
  49. Casein kinase Ialpha (CKIalpha) phosphorylates FADD at Ser194 both in vitro and in vivo. Phosphorylation of FADD by CKI is a crucial event during mitosis. PMID: 16061179
  50. FADD plays a dispensable role during thymocyte development, but is essential in maintaining peripheral T cell homeostasis. and regulating both apoptotic and proliferation signals. PMID: 16116191

Show More

Hide All

Database Links
icon of phone
Call us
301-363-4651 (Available 9 a.m. to 5 p.m. CST from Monday to Friday)
icon of address
7505 Fannin St., Ste 610, Room 322 (CUBIO Innovation Center), Houston, TX 77054, USA
icon of social media
Join us with

Subscribe newsletter

Leave a message

* To protect against spam, please pass the CAPTCHA test below.
CAPTCHA verification
© 2007-2024 CUSABIO TECHNOLOGY LLC All rights reserved. 鄂ICP备15011166号-1