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. [provided by RefSeq, Jul 2008]
SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
TNFRSF13B-20-RE | 20 (40 μL) | 200 μL | Request Pricing | |
TNFRSF13B-20-OR | 20 (40 μL) | 200 μL | Request Pricing | |
TNFRSF13B-20-GO | 20 (40 μL) | 200 μL | Request Pricing | |
TNFRSF13B-20-GR | 20 (40 μL) | 200 μL | Request Pricing | |
TNFRSF13B-20-AQ | 20 (40 μL) | 200 μL | Request Pricing |
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. [provided by RefSeq, Jul 2008]
Gene Symbol : TNFRSF13B
Gene Name : TNF receptor superfamily member 13B
Chromosome : CHR 17: 169,720,87-169,390,83
Locus : 17p11.2
Alt. Genes : ATP6AP2
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