Recombinant Mouse T-lymphocyte activation antigen CD86 (Cd86), partial

Code CSB-YP004965MO1
MSDS
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Source Yeast
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Code CSB-EP004965MO1
MSDS
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Source E.coli
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Code CSB-EP004965MO1-B
MSDS
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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.
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Code CSB-BP004965MO1
MSDS
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Source Baculovirus
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Code CSB-MP004965MO1
MSDS
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Source Mammalian cell
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Product Details

Purity
>85% (SDS-PAGE)
Target Names
Cd86
Uniprot No.
Alternative Names
Cd86; T-lymphocyte activation antigen CD86; Activation B7-2 antigen; Early T-cell costimulatory molecule 1; ETC-1; CD antigen CD86
Species
Mus musculus (Mouse)
Protein Length
Partial
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.
Form
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
Reconstitution
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.
Notes
Repeated freezing and thawing is not recommended. Store working aliquots at 4°C for up to one week.
Datasheet
Please contact us to get it.

Customer Reviews and Q&A

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Target Background

Function
Receptor involved in the costimulatory signal essential for T-lymphocyte proliferation and interleukin-2 production, by binding CD28 or CTLA-4. May play a critical role in the early events of T-cell activation and costimulation of naive T-cells, such as deciding between immunity and anergy that is made by T-cells within 24 hours after activation. Also involved in the regulation of B cells function, plays a role in regulating the level of IgG(1) produced. Upon CD40 engagement, activates NF-kappa-B signaling pathway via phospholipase C and protein kinase C activation.
Gene References into Functions
  1. Our results reveal a role for B7-2 as obligatory receptor for superantigens. B7-2 homodimer interface mimotopes prevent superantigen lethality by blocking the superantigen-host costimulatory receptor interaction. PMID: 27708164
  2. results suggest that the TLR2-p38-CD86 signaling pathway plays a vital role in inflammation associated with burn injury PMID: 28460187
  3. role with CD40 in primary germinal center generation of distinct antigen-presenting cells PMID: 28768709
  4. B7.2 expressed on skin CD8(+) T cells supports the survival of Tregs, likely through interaction with its receptor CTLA-4, which is highly expressed on skin Tregs. PMID: 27183612
  5. Low CD86 expression is associated with B16 melanoma. PMID: 26485753
  6. Local administration of CD86 siRNA during the effector phase ameliorates asthma phenotypes. PMID: 25344652
  7. Meningococcal capsular polysaccharide-loaded vaccine nanoparticles induce expression of CD86. PMID: 24981893
  8. novel function of CTLA4Ig in tumor immunity and suggest that CD86 on NK cells is an activating receptor and closely involved in the CTLA4Ig-mediated anti-tumor response. PMID: 24349559
  9. CD4(+) NKG2D(+) T cells induce NKG2D down-regulation in natural killer cells in CD86-RAE-1epsilon transgenic mice. PMID: 24708417
  10. CD86 expression has functional consequences for the magnitude of CD4 T cell responses both in vitro and in vivo. These data pinpoint CD86 upregulation as an additional mechanism by which IL-21 can elicit immunomodulatory effects. PMID: 24470500
  11. the results presented here demonstrate that recruitment and expression of MHC-II, CD80, CD86, PDL1, and PD-L2 in M of peritoneal cavity in T. crassiceps early at infection is associated to the sex of the host. PMID: 23533995
  12. Combinatorial signaling through TLR-2 and CD86 augments B-cell receptor-free activation and differentiation of resting B cells. PMID: 23365665
  13. Phb1/2 and the CD86 cytoplasmic domain cooperate to mediate CD86 signaling in a B cell through differential phosphorylation of distal signaling intermediates required to increase IgG1. PMID: 23241883
  14. In response to Pseudomonas infection, mobilized neutrophils upregulate and provide B7 trans-costimulatory signals to T cells, preventing established lung allograft tolerance. PMID: 23018463
  15. Data indicate that most toll-like receptor (TLR) ligands induced comparable upregulation of co-stimulatory molecules CD40, CD86 and B7H1 on young and aged conventional dendritic cells (cDC). PMID: 22231652
  16. Interaction between CD28 and B7 molecules is required for regulation of splenic and bone marrow plasma cells. PMID: 22908331
  17. B7 and CD28 interactions promote the proliferation and survival of murine gammadelta T cells following Plasmodium infection. PMID: 22732586
  18. Yeast-derived beta-glucan lacks cytotoxic effects towards B-lymphoma cells but up-regulation of CD86 suggests maturation of the cells via dectin-1 by the carbohydrate PMID: 22199280
  19. Ubiquitin-mediated regulation of CD86 protein expression by the ubiquitin ligase membrane-associated RING-CH-1 (MARCH1). PMID: 21896490
  20. Parasite-induced B7-2 is dependent on Jun N-terminal protein kinase (JNK) but not extracellular signal-regulated kinase or p38 signaling; its expression on human peripheral blood monocytes is dependent on JNK signaling. PMID: 21911468
  21. These studies suggest that ubiquitination serves as an important mechanism by which dendritic cells control CD86 expression PMID: 21849678
  22. T-cell costimulation via B7 ligands (CD80 and CD86) is essential for development of experimental hypertension; inhibition of this process could have therapeutic benefit in the treatment of this disease. PMID: 21126972
  23. CD86 is critical for naive CD4+ T cell activation in vivo and differentiation into either a Th1 or Th2 phenotype. PMID: 11937530
  24. B7-2 in deleting pathogenic autoreactive T cells in the thymus. PMID: 11956287
  25. B cell-associated B7-2 expression is regulated by stimulation of the B cell receptor and/or the beta 2-adrenergic receptor in vivo and in vitro. PMID: 12055247
  26. Activation-induced up-regulation of B7-2 on antigen presenting cells leads to increased CD28 signaling and a commitment to cross-priming of CD4-dependent cytotoxic T lymphocytes. PMID: 12370335
  27. Role of CD86 in enhancing cell-cycle progression and survival of CD4(+) T lymphocytes after activation. PMID: 12429713
  28. fate of LACK-specific CD4+ T cells in Leishmania-infected BALB/c mice which have been treated or not with anti-CD86 mAb PMID: 12516542
  29. Although CD86 plays a critical role in T-dependent IgG and IgE responses of B cells to in vivo antigenic challenge, direct CD86 signaling of a B cell is not essential for its efficient activation. PMID: 12517941
  30. Stimulation by CD86, either alone or together with beta 2-AR on a CD40ligand/IL-4 activated B cell, increases both the level and the rate of mature IgG1 transcription without affecting transcript stability or class switching to IgG1. PMID: 12734361
  31. B7-2 and B7-1 have overlapping functions in the endogenous superantigen-mediated deletion of TCR V beta 11- or V beta 12-bearing thymocytes. PMID: 12759417
  32. B7-2 overexpressed on transgenic donor T cells mediates reduced alloresponsiveness and mortality in graft-vs-host disease compared with wild-type T cells. PMID: 14688306
  33. stimulation of matured bone marrow dendritic cells with anti-CD80 monoclonal antibody up-regulated CD86 levels on the cell surface Coculture of these cells with naive, allogeneic T cells downregulated Th1 responses and upregulated suppressor responses PMID: 14966193
  34. T cells activated in the presence of parenchymal cells from the eye express B7-2 in a manner that equips them to suppress bystander T cells. Thus, B7-2 expression on T cells participates in their eventual ability to function as regulators in vitro. PMID: 15034031
  35. increased surface expression on Mycobacterium tuberculosis secretory antigen (MTSA)activated dendritic cells after stimulation with M. tuberculosis cell extract downregulates the Th1 cells response to Mycobacterial antigens PMID: 15116295
  36. B7-2 plays a critical role in priming pancreatic islet-reactive CD4 T cells: B7-2 deficiency causes a profound diminishment in the generation of spontaneously activated CD4 T cells and islet-specific CD4 T cell expansion. PMID: 15356107
  37. Increased B7-2 expression on islet-infiltrated nonobese diabetic (NOD) mouse B cells is associated with increased T cell costimulation and the development of inflammatory insulitis in NOD mice. PMID: 15634886
  38. CD86 plays a critical role in induction of anterior chamber-associated immune deviation. PMID: 15778288
  39. Could not be expressed on keratinocyte stem cells. PMID: 15808622
  40. upregulated in SV5 infection of dendritic cells in both BALB/c and C57BL/6 mice strains PMID: 15919909
  41. Tolerance may be induced by B7-driven negative regulatory signaling, but tolerance is maintained by a lack of signal 2 (B7.2), because expression of B7 is eventually lost in vivo. PMID: 16002674
  42. CD86 is protective in glomerulonephritis by enhancing Th2 and attenuating Th1 responses PMID: 16014035
  43. CD86 is not required for oral tolerization. PMID: 16439314
  44. CD86 induces a previously unknown signal transduction pathway that regulates the level of B cell gene expression and activity proximal to NF-kappa B activation. PMID: 16709832
  45. B7-1 and B7-2 differently contribute to the development of T cell-mediated experimental allergic conjunctivitis during the induction and effector phases PMID: 17109973
  46. Data indicate that anti-B7-2 monoclonal antibody B7 molecules can trigger innate-effector responses in macrophages by activating NF-kappaB, and are not only essential for induction of adaptive immune responses but also play roles in innate immunity. PMID: 17314080
  47. B7-2 promotes the generation of a mature antigen-presenting cell (APC) repertoire and promotes APC function and survival. PMID: 17475851
  48. Either CD80- or CD86-costimulation is indispensable for induction of oral sensitization and IgE-mediated hypersensitivity to peanut, with CD86 being the most important ligand in inducing peanut extract-specific IgE responses. PMID: 17513738
  49. CD86 plays a key role in regulating the level of B-cell IgG1 produced in vitro and in vivo. PMID: 17641017
  50. while CD86 does not stimulate an initial response as strongly as CD80, there is greater sustained activity that is seen even in the absence of continued costimulation PMID: 17947667

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Subcellular Location
Cell membrane; Single-pass type I membrane protein.
Tissue Specificity
Expressed on activated B-cells.
Database Links
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