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TNFRSF13B

Anti-TNFRSF13B Products
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- Type: Mouse IgG1
- Application: ELISA, FC
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- Type: Mouse IgG1
- Application: ELISA, FC
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- Type: Mouse IgG1
- Application: ELISA, IHC, FC
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- Species Reactivity: Human
- Type: Mouse IgG2a
- Application: FC, FuncS
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- Species Reactivity: Human
- Application: IHC-Fr, Neut, WB
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- Derivation: Mouse
- Species Reactivity: Human
- Type: Mouse IgG2b
- Application: WB, ELISA, FC
- Mouse Anti-TNFRSF13B Recombinant Antibody (clone 9D22) (NEUT-2120CQ)
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- Species Reactivity: Human
- Type: Mouse IgG1
- Application: IHC, Neut, WB
- Mouse Anti-TNFRSF13B Recombinant Antibody (clone CBL172) (NEUT-2123CQ)
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- Species Reactivity: Human
- Type: Mouse IgG1
- Application: IHC, Neut, WB
- Mouse Anti-TNFRSF13B Recombinant Antibody (clone CBL339) (NEUT-2122CQ)
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- Species Reactivity: Human
- Type: Mouse IgG1
- Application: Block, WB, IHC
- Mouse Anti-TNFRSF13B Recombinant Antibody (clone CBL338) (NEUT-2121CQ)
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- Species Reactivity: Human
- Type: Mouse IgG1
- Application: Block, CyTOF, FC
- PE-B7/Human TNFRSF13B (SPALPGLKL) MHC Tetramer (MHC-LC1968)
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- Class: Class I
- Antigen: TNFRSF13B
- Antigen Species: Human
- Peptide: SPALPGLKL
- Conjugate: PE
- Anti-Mouse TNFRSF13B Immunohistochemistry Kit (VS-0525-XY7373)
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- Species Reactivity: Mouse
- Target: TNFRSF13B
- Application: IHC
- Anti-TNFRSF13B Immunohistochemistry Kit (VS-0525-XY7372)
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- Species Reactivity: Human
- Target: TNFRSF13B
- Application: IHC
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- Species Reactivity: Human
- Type: Rabbit IgG
- Application: FC, ELISA
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- Species Reactivity: Mouse
- Type: Rat IgG2a, kappa
- Application: FC
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- Species Reactivity: Human
- Type: Rabbit IgG
- Application: ELISA
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For Research Use Only. Not For Clinical Use.
The protein encoded by this gene is a lymphocyte-specific member of the tumor necrosis factor (TNF) receptor superfamily. It interacts with calcium-modulator and cyclophilin ligand (CAML). The protein induces activation of the transcription factors NFAT, AP1, and NF-kappa-B and plays a crucial role in humoral immunity by interacting with a TNF ligand. This gene is located within the Smith-Magenis syndrome region on chromosome 17.