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Rat Anti-KLRB1 Recombinant Antibody (A1366) (CBMAB-AP5095LY)

The product is antibody recognizes NKRP1A. The antibody A1366 immunoassay techniques such as: FC.
See all KLRB1 antibodies

Summary

Host Animal
Rat
Specificity
Mouse
Clone
A1366
Antibody Isotype
IgG2a
Application
FC

Basic Information

Specificity
Mouse
Antibody Isotype
IgG2a
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

Formulations & Storage [For reference only, actual COA shall prevail!]

Format
Liquid
Purity
Affinity purity
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freezethaw cycles.

Target

Full Name
Killer Cell Lectin Like Receptor B1
Entrez Gene ID
UniProt ID
Alternative Names
Killer Cell Lectin Like Receptor B1, Natural Killer Cell Surface Protein P1A, C-Type Lectin Domain Family 5 Member B, HNKR-P1A, CLEC5B, NKRP1A, CD161 Antigen, NKR
Function
Plays an inhibitory role on natural killer (NK) cells cytotoxicity. Activation results in specific acid sphingomyelinase/SMPD1 stimulation with subsequent marked elevation of intracellular ceramide. Activation also leads to AKT1/PKB and RPS6KA1/RSK1 kinases stimulation as well as markedly enhanced T-cell proliferation induced by anti-CD3. Acts as a lectin that binds to the terminal carbohydrate Gal-alpha(1,3)Gal epitope as well as to the N-acetyllactosamine epitope. Binds also to CLEC2D/LLT1 as a ligand and inhibits NK cell-mediated cytotoxicity as well as interferon-gamma secretion in target cells.
Biological Process
Cell surface receptor signaling pathwayManual Assertion Based On ExperimentTAS:ProtInc
Cellular Location
Membrane
Topology
Cytoplasmic: 1-44
Helical: 45-66
Extracellular: 67-225
PTM
N-glycosylated. Contains sialic acid residues.

Xu, N., Meng, X., Chu, H., Yang, Z., Jiao, Y., & Li, Y. (2023). The prognostic significance of KLRB1 and its further association with immune cells in breast cancer. PeerJ, 11, e15654.

Huang, G., Xiao, S., Jiang, Z., Zhou, X., Chen, L., Long, L., ... & Jiang, B. (2023). Machine learning immune-related gene based on KLRB1 model for predicting the prognosis and immune cell infiltration of breast cancer. Frontiers in Endocrinology, 14, 1185799.

Cheng, X., Cao, Y., Wang, X., Cheng, L., Liu, Y., Lei, J., ... & Shi, D. (2022). Systematic pan-cancer analysis of KLRB1 with prognostic value and immunological activity across human tumors. Journal of immunology research, 2022.

Di, W., Fan, W., Wu, F., Shi, Z., Wang, Z., Yu, M., ... & Zhang, W. (2022). Clinical characterization and immunosuppressive regulation of CD161 (KLRB1) in glioma through 916 samples. Cancer Science, 113(2), 756-769.

Hachim, M., Hachim, I., & Hannawi, S. (2022). Killer cell lectin-like receptor subfamily B member 1 (KLRB1), lymphocyte function-associated antigen 3 (CD58), and Niban1 (FAM129A) are unique markers for developed (central and effector) memory T cells in rheumatoid arthritis. Saudi Medical Journal, 43(6).

Lu, J., Bi, Y., Zhu, Y., Huipeng, S., Duan, W., & Zhou, J. (2021). CD3D, GZMK, and KLRB1 are potential markers for early diagnosis of rheumatoid arthritis, especially in anti-citrullinated protein antibody-negative patients. Frontiers in Pharmacology, 12, 726529.

Zhang, G., Liu, Y., Dong, F., & Liu, X. (2020). Transcription/expression of KLRB1 gene as a prognostic indicator in human esophageal squamous cell carcinoma. Combinatorial Chemistry & High Throughput Screening, 23(7), 667-674.

Thude, H., Rother, S., Sterneck, M., Klempnauer, J., Nashan, B., Schwinzer, R., & Koch, M. (2018). The killer cell lectin‐like receptor B1 (KLRB1) 503T> C polymorphism (rs1135816) and acute rejection after liver transplantation. Hla, 91(1), 52-55.

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For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

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