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  5. TNF-alpha
  6. TNF alpha/TNFSF2 protein, Human (His)

Tumour Necrosis Factor alpha (TNF alpha) is a potent pro-inflammatory cytokine. TNF alpha binds to its receptors, mainly TNFR1 and TNFR2, and then transmits molecular signals for biological functions such as inflammation and cell death. TNF alpha stimulates NF-κB pathway via TNFR2 promotes cancer growth, invasion, and metastasis. Anti-TNF-α MAb significantly suppresses the tumor development in colitis-associated cancer (CAC) mouse. TNF alpha as a proneurogenic factor activates the SAPK/JNK Pathway and can facilitate neuronal replacement and brain repair in response to brain injury. TNF alpha/TNFSF2 protein, Human (His) is a recombinant protein with a N-Terminal His label, It consists of 157 amino acids (V77-L233) and is produced in CHO cells.

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Top Publications Citing Use of Products

    TNF alpha/TNFSF2 protein, Human (His) purchased from MCE. Usage Cited in: J Immunother Cancer. 2025 Nov 28;13(11):e011976.  [Abstract]

    Western blot analysis of CD155 expression in OS cells treated with exogenous TNF-α, showing concentration- and time-dependent upregulation. TNF-α at increasing concentrations (0, 10, 20, 30 ng/mL for 24 hours) and varying time points (0, 6, 12, 24 hours at 10 ng/mL) upregulates CD155 in U2OS and K7M2 cells. GAPDH serves as a loading control.

    TNF alpha/TNFSF2 protein, Human (His) purchased from MCE. Usage Cited in: Int J Mol Med. 2026 Feb;57(2):43.  [Abstract]

    Autophagic flux was measured by transfecting cells with mRFP-GFP-LC3 dual-fluorescence adenovirus (Ad-LC3), allowing differentiation between autophagosomes (mRFP+/GFP+ fluorescence, appearing as yellow puncta) and autolysosomes (mRFP+/GFP-fluorescence, appearing as red puncta). TNF-α (200 ng/ml) induced epithelial cells for 48 h. Representative immunofluorescence images were shown. (Original magnification, ×20). Quantification of LC3 puncta number of representative cells.

    TNF alpha/TNFSF2 protein, Human (His) purchased from MCE. Usage Cited in: Int J Mol Med. 2026 Feb;57(2):43.  [Abstract]

    Relative glucose content and lactate (Lac) production in control vs. TNF-α (200 ng/ml, 24 h) induced epithelial cells.

    TNF alpha/TNFSF2 protein, Human (His) purchased from MCE. Usage Cited in: Int J Mol Med. 2026 Feb;57(2):43.  [Abstract]

    BCECF fluorescent counter-staining in TNF-α (200 ng/ml, 24 h) induced epithelial cells vs. control. Representative immunofluorescence images were shown.

    TNF alpha/TNFSF2 protein, Human (His) purchased from MCE. Usage Cited in: Sci Adv. 2023 Oct 6;9(40):eadi8343.  [Abstract]

    U2OS cells were treated with TNF-α (20 ng/ml) for 24 hours. The protein levels of p300 and LAMP2A were measured using immunoblot analyses.
    • Actividad biológica

    • Technical Parameters

    • Properties

    • Descripciòn

    • Referencias

    Descripciòn

    Tumour Necrosis Factor alpha (TNF alpha) is a potent pro-inflammatory cytokine[1]. TNF alpha binds to its receptors, mainly TNFR1 and TNFR2, and then transmits molecular signals for biological functions such as inflammation and cell death[2]. TNF alpha stimulates NF-κB pathway via TNFR2 promotes cancer growth, invasion, and metastasis. Anti-TNF-α MAb significantly suppresses the tumor development in colitis-associated cancer (CAC) mouse[3]. TNF alpha as a proneurogenic factor activates the SAPK/JNK Pathway and can facilitate neuronal replacement and brain repair in response to brain injury[4]. TNF alpha/TNFSF2 protein, Human (His) is a recombinant protein with a N-Terminal His label, It consists of 157 amino acids (V77-L233) and is produced in CHO cells.

    Background

    TNF alpha is produced by various types of cells including macrophages, monocytes, neutrophils, T cells, and NK-cells[2].
    The amino acid sequence of human TNF alpha protein has low homology between mouse, rat, bovine, cynomolgus TNF alpha protein. While, human TNF alpha shares 94.85% aa sequence identity with cynomolgus TNF alpha protein, mouse TNF alpha shares 94.47% aa sequence identity with rat TNF alpha protein.
    TNF alpha exists in two forms; a type II transmembrane protein (tmTNF-α) and a mature soluble protein (sTNF-α). TNF-α binds to its receptors, mainly TNFR1 and TNFR2, and then transmits molecular signals for biological functions such as inflammation and cell death. Both sTNF-α and tmTNF-α activate TNFR1, and process a death domain (DD) that interacts with the TNFR1-associated death domain (TRADD) adaptor protein. The TNFR2 signaling pathway is mainly activated by tmTNF-α. TNFR1 signaling tends to be pro-inflammatory and apoptotic. TNFR2 results in NF-κB and MAPKs and AKT activation, TNFR2 activation is associated with homeostatic bioactivities such as tissue regeneration, cell proliferation, and cell survival, as well as host defense and inflammation[1].
    TNF-alpha is critical for normal immune response, abnormal secretion TNF alpha activates synovial fibroblasts, keratinocytes, osteoclasts, induces rheumatoid arthritis, inflammatory bowel disease, psoriatic arthritis (PsA), and noninfectious uveitis (NIU)[3]. TNF alpha positively regulates endogenous TNF-α expression levels independently of Pgp efflux activity, induces IHF cells proliferation[4]. TNF alpha in tissues may promote cancer growth, invasion, and metastasis. Besides, TNF alpha stimulates NF-κB pathway via TNFR2 and anti-TNF-α MAb significantly suppresses the tumor development in colitis-associated cancer (CAC) mouse[5]. TNF alpha as a proneurogenic factor activates the SAPK/JNK pathway and can facilitate neuronal replacement and brain repair in response to brain injury[6].

    In Vitro

    TNF alpha (human) (0, 10, 15, 20, 30, 50 ng/mL; 24, 48 h) reduces KB-C1 cells viability at 30 ng/mL after 48 h, reduces pro-caspase-3, cleaved caspase-3 expression in KB-C1 and KB-3-1 cells[4].
    TNF alpha (human) (10, 15 ng/mL; 24 h) significantly increases the mRNA levels of Pgp (ABCB1) in KB-3-1 cells, and promotes expressive reduction on total Pgp protein levels and a slightly decreases in cell surface-Pgp in KB-C1 cells, and stimulates IHF cells proliferation, probably via ERK activation[4].

    In Vivo

    TNF alpha (human) (100 µg; osmium pump in back; daily for 7 days) significantly increases in the number of inflammatory cells and the degree of synovial inflammation is significantly exacerbated in twenty-four SCID-HuRAg mice[7].

    Actividad biológica

    1. Measured in a cytotoxicity assay using L-929 mouse fibroblast cells in the presence of the metabolic inhibitor actinomycin D. The ED50 for this effect is < 0.13 ng/mL.
    2. Loaded Brivekimig (HY-P990907) on AHC2 biosensor, can bind TNF alpha protein, Human (His) with an affinity constant of <1.0E-12 M as determined in BLI assay.

    • Measured in a cytotoxicity assay using L-929 mouse fibroblast cells in the presence of the metabolic inhibitor actinomycin D. The ED50 for this effect is 0.4678 pg/mL, corresponding to a specific activity is 2.137×109 units/mg.
    • Loaded Brivekimig (HY-P990907) on AHC2 biosensor, can bind TNF alpha protein, Human (His) with an affinity constant of <1.0E-12 M as determined in BLI assay.
    Species

    Human

    Source

    E. coli

    Tag

    N-6*His

    Accession

    P01375 (V77-L233)

    Gene ID
    Molecular Construction
    N-term
    6*His
    TNF alpha (V77-L233)
    Accession # P01375
    C-term
    Protein Length

    Full Length of TNF soluble form

    Synonyms
    Tumor Necrosis Factor; Cachectin; TNF-Alpha; Tumor Necrosis Factor Ligand Superfamily Member 2; TNF-a; TNF; TNFA; TNFSF2
    AA Sequence

    VRSSSRTPSDKPVAHVVANPQAEGQLQWLNRRANALLANGVELRDNQLVVPSEGLYLIYSQVLFKGQGCPSTHVLLTHTISRIAVSYQTKVNLLSAIKSPCQRETPEGAEAKPWYEPIYLGGVFQLEKGDRLSAEINRPDYLDFAESGQVYFGIIAL

    Predicted Molecular Mass
    17.4 kDa
    Peso molecular

    Approximately 18 kDa, based on SDS-PAGE under reducing conditions.

    Pureza
    • ≥ 90%, as determined by reducing SDS-PAGE.
    Appearance

    Lyophilized powder

    Formulation

    1.Lyophilized from a 0.22 μm filtered solution of PBS, 300 mM NaCl, pH 7.4.
    2.Lyophilized from a 0.22 μm filtered solution of PBS.
    3.Lyophilized from a 0.22 μm filtered solution of PBS, pH 6.5, 8% trehalose.
    Please refer to the lot-specific COA for specific buffer information.

    Endotoxin Level

    <1 EU/μg, determined by LAL method.

    Reconstitution

    It is not recommended to reconstitute to a concentration less than 100 μg/mL in ddH2O. For long term storage it is recommended to add a carrier protein (0.1% BSA, 5% HSA, 10% FBS or 5% Trehalose).

    Storage & Stability

    Stored at -20°C for 2 years from date of receipt. After reconstitution, it is stable at 4°C for 1 week or -20°C for longer (with carrier protein). It is recommended to freeze aliquots at -20°C or -80°C for extended storage.

    Envío

    Room temperature in continental US; may vary elsewhere.

    Documentación
    Referencias
    Help & FAQs
    • Do most proteins show cross-species activity?

      Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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    The reconstitution calculator equation

    Volume (to add to vial) = Mass (in vial) ÷ Desired Reconstitution Concentration

    Volume (to add to vial) = Mass (in vial) ÷ Desired Reconstitution Concentration
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    The dilution calculator equation

    Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

    This equation is commonly abbreviated as: C1V1 = C2V2

    Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
    × = ×
    C1   V1   C2   V2

    The specific activity calculator equation

    Specific Activity (Unit/mg) = 106 ÷ Biological Activity (ED50)

    Specific Activity (Unit/mg) = 106 ÷ Biological Activity (ED50)
    Unit/mg = 106 ÷ ng/mL

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    Inquiry Information

    Nombre del producto:
    TNF alpha/TNFSF2 protein, Human (His)
    Cat. No.:
    HY-P70426A
    Cantidad:
    MCE Japan Authorized Agent: