Recombinant hCD154-muCD8

SKU:BHP14700005
Research Validated
Overview
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Recombinant human Murine CD8α Fusion (muCD8) expressed in CHO Cells cells. Validated for ELISA and Flow Cytometry. Human origin. Available unconjugated and conjugated (Biotin, FITC, PE).
Expression System CHO Cells
Fusion Format Murine CD8α Fusion
Molecular Weight 19kD
Species Reactivity Human
Storage 2–5°C
Validated Applications ELISA, Flow Cytometry, Western Blot
Options selector
Catalog no. Form Size
505-020 Purified (with Antibiotic)
505-820 Purified (Preservative-free)
505-030 Biotin conjugate
Available Options

Select the variant that best fits your experiment. Availability and lead time may vary by option.

  • Options: Form (3) – Purified (with Antibiotic), Purified (Preservative-free), Biotin conjugate | Size: 25 µg
  • Lead time: options listed in "Availability Content"; other statuses may take longer.
  • Storage: Store at 2 - 5°C. Freeze/Thawing is not recommended.
  • Shipping: cold-chain shipment (typically with ice packs).
  • Upon receipt: refrigerate upon receipt.
  • Sales terms and conditions: Please review prior to ordering.
Field Specification
Mfr No 505
Alternative Names CD40L, CD40 Ligand, gp39
Conjugate
  • Biotin
  • Unconjugated
Formulation 50 mM Sodium Phosphate pH 7.5, 100 mM Potassium Chloride, 150mM NaCl, 0.5% Gentamicin sulfate
Host CHO cells
Product Type
  • Recombinant Protein
Shipping Shipped on blue ice
Storage Store at 2 - 5°C. Freeze/Thawing is not recommended.

Scientific Background

Human CD154 (CD40 Ligand) is a member of the tumor necrosis factor (TNF) family and is expressed on the surface of activated T cells. It can undergo proteolytic cleavage into a 19kD immunologically active soluble form. Interaction of CD154 and CD40 is essential for isotype switching in B cells. Known genetic defects that alter this interaction lead to impaired immune system function (1). Increased levels of CD154 has been associated with autoimmune disorders including SLE, CLL and eosinophilic fasciitis (5,9,10,11). CD154 has been reported to be expressed on vascular endothelial cells, smooth muscle cells, macrophages and activated platelets indicating a role for the CD40-CD154 immunoregulatory signaling in arthrosclerosis and cardiovascular disorders (7,12,13).

Product Description

CHO Cells

Recombinant hCD154-muCD8 is a recombinant human fusion protein produced in CHO Cells cells. Molecular Structure: A soluble molecule consisting of the extracellular domain (213aa) of human CD154 fused to the extracellular domain (167aa) of murine CD8 alpha, with a predicted monomeric molecular weight of 42.6 kd. A similar construct described in reference (9).

Alternative names: CD40L, CD40 Ligand, gp39

Protein Specifications

Fusion Format Murine CD8α Fusion (muCD8)
Expression System CHO Cells
Molecular Weight 19kD
Formulation 50 mM Sodium Phosphate pH 7.5, 100 mM Potassium Chloride, 150mM NaCl, 0.5% Gentamicin sulfate
Storage Store at 2 - 5°C. Freeze/Thawing is not recommended.
Species Reactivity Human, Pig, Dog, Mouse
Validated Applications ELISA, Flow Cytometry, Western Blot
Available Conjugates Biotin, Unconjugated

✔ Research Use Only (RUO)

Functional Activity

Human CD154-muCD8 binds to cell surface expressed human CD40 and this binding is blocked by anti-human CD154 monoclonal antibody. Recombinant CD154-muCD8 has been shown to induce phosphorylation of ERK, JNK and p38 molecules and subsequent activation of NFkB pathway (14, 15, 16) and to stimulate B cell proliferative response (19, 21). It crossreacts with CD40 in other species including pig (17)and dog(18).

Safety & Handling

Research Use Only. Not intended for diagnostic, therapeutic, or clinical use. Handle according to good laboratory practice (GLP). Consult the Safety Data Sheet (SDS) prior to use.

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What expression system was used to produce Recombinant hCD154-muCD8?

This protein was expressed in CHO Cells cells. Mammalian expression is critical for this Fc fusion protein because it ensures proper glycosylation and tertiary folding of the extracellular immunoglobulin-like domains, preserving native receptor-binding activity.

Which applications has this product been validated for?

Recombinant hCD154-muCD8 has been validated for: ELISA, Flow Cytometry, Western Blot. It is produced as a Murine CD8α Fusion (muCD8), making it suitable as a blocking reagent, binding standard, or functional stimulant/inhibitor in immunology assays.

How should I store this product?

Recommended storage: Store at 2 - 5°C. Freeze/Thawing is not recommended.. Formulation: 50 mM Sodium Phosphate pH 7.5, 100 mM Potassium Chloride, 150mM NaCl, 0.5% Gentamicin sulfate. Avoid repeated freeze-thaw cycles. If long-term storage is needed, aliquot upon first use.

What species does this fusion protein cross-react with?

Species reactivity includes: human, pig, dog, mouse. Cross-reactivity was confirmed by functional binding assays (e.g., ELISA and/or FACS) against cells or recombinant proteins from the indicated species.

What conjugate formats are available for this product?

Available formats include: Biotin, Unconjugated. Conjugated forms are ready-to-use without secondary detection reagents for flow cytometry. Unconjugated (purified) forms can be used with anti-Fc secondary antibodies in ELISA.

Can't Find What You're Looking For? We can help you source the best match or customize a recombinant protein solution for your study. Options may include species (human/mouse/rat), protein region/domain (full-length vs fragment), tag or label (His/GST/FLAG/biotin/fluorescent), expression system (E. coli/HEK293/insect), purity grade, formulation (buffer, carrier-free, glycerol-free), activity/functional validation (binding or enzymatic assays), endotoxin level (low-endotoxin for cell-based work), mutants/variants (point mutations, isoforms), and bulk or custom packaging. Click Talk to a Scientist to submit a request form, email us at support@biohippo.com, or explore our Research Services for additional support. Our team will be in contact with you shortly.

  1. D. Gray, et al, (1994) Seminars in Immunol 6: 303-310.
  2. A.C. Grammer, et al, (1995) J Immunol 154: 4996-5010.
  3. F. Pietravalle, et al, (1996) J Biol Chemistry 271: 5965-5967.
  4. R.J. Noelle, (1996) Immunity 4: 415-419.
  5. A. Desai-Mehta, et al, (1996) J Clin Invest 97: 2063-2073.
  6. I.S. Grewal and R.A. Flavell, (1996) Immunol Today 17: 410-414.
  7. F. Mach, et al, (1997) Proc Natl Acad Sci USA 94:1931-1936.
  8. A.C. Grammer, et al, (1999) J Immunol 163: 4150-4159.
  9. D. Hollenbaugh, (1992) EMBO 11: 4314-4321.
  10. R.K. Vakkalanka, et al, (1999) Arthritis Rhem 42:871-81.
  11. M. Jinnin, et al.(2003) Ann Rhem Dis 62: 190-191.
  12. U. Schonbeck, et al, (2000) PNAS USA 97: 7458-7463.
  13. U. Schonbeck, et al, (2001) Circulation 104: 2266-2268.
  14. AC Grammer, PF Lipsky, et al (2000) Advances in Immunology 76: 61-178.
  15. AC Grammer, PF Lipsky, et al (2004) Arthristis Research and Therapy 6: 28-38.
  16. Melter M, D M Briscoe, et al (2000) Blood 96:3801-3808.
  17. Takamatsu H, RME Parkhouse, et al. (1999) Immunology 97(2):211-213.
  18. Daisuke I, J F Modiano, et al. (2012) Leukemia and Lymphoma 53(7): 1390-1398
  19. Brodeur SR, RS Geha, et al. (2003) Immunity 18(6): 837-848
  20. KC Bankert, GA Bishop, et al.(2015) J Immunol 194(9): 4319-4327. PMID: 25795759.ID:
  21. CR Smulski, S Fournel, et al. (2017) Cell Death and Disease 8(2):e2601. doi: 10.1038/cddis.2017.22. PMID: 28182009
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