IL1RAPL1 antibody [3R16]

Cannot supply to this region.

SKU:: GTX52806
Additional Names:: IL1R8 , IL1RAPL , IL1RAPL1 , MRX10 , MRX21 , MRX34 , OPHN4 , TIGIRR2 , interleukin 1 receptor accessory protein like 1
Application:: WB
Concentration:: 500 ug/ml
Physical State:: Liquid
Species Reactivity:: Human
Purification:: Protein G Purified
Storage Conditions:: -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
Supplier:: Genetex
Host:: Mouse
Reactivities:: Human
Buffer:: PBS, no preservatives.
Immunogen:: Human recombinant IL1-R8 EC domain
Clone:: 3R16
Uniprot:: Q9NZN1
Synonyms:: IL-1-RAPL-1;IL-1RAPL-1;IL1R8;IL1RAPL;IL1RAPL-1;interleukin 1 receptor-8;interleukin-1 receptor accessory protein-like 1;mental retardation, X-linked 10;MRX10;MRX21;MRX34;oligophrenin-4;OPHN4;three immunoglobulin domain-containing IL-1 receptor-related 2;TIGIRR-2;X-linked interleukin-1 receptor accessory protein-like 1
Extra Details:: The protein encoded by this gene is a member of the interleukin 1 receptor family and is similar to the interleukin 1 accessory proteins. This protein has an N-terminal signal peptide, three extracellular immunoglobulin Ig-like domains, a transmembrane domain, an intracellular Toll/IL-1R domain, and a long C-terminal tail which interacts with multiple signalling molecules. This gene is located at a region on chromosome X that is associated with a non-syndromic form of X-linked intellectual disability. Deletions and mutations in this gene were found in patients with intellectual disability. This gene is expressed at a high level in post-natal brain structures involved in the hippocampal memory system, which suggests a specialized role in the physiological processes underlying memory and learning abilities, and plays a role in synapse formation and stabilization. [provided by RefSeq, Jul 2017]

Shipping Conditions:: Blue Ice