TBLR1 (TBL1XR1) (NM_024665) Human Recombinant Protein
CAT#: TP760864
Purified recombinant protein of Human transducin (beta)-like 1 X-linked receptor 1 (TBL1XR1), full length, with N-terminal HIS tag, expressed in E. coli, 50ug
Other products for "TBL1XR1"
Specifications
Product Data | |
Species | Human |
Expression Host | E. coli |
Expression cDNA Clone or AA Sequence |
A DNA sequence encoding human full-length TBL1XR1
|
Tag | N-His |
Predicted MW | 55.4 kDa |
Concentration | >50 ug/mL as determined by microplate BCA method |
Purity | > 80% as determined by SDS-PAGE and Coomassie blue staining |
Buffer | 25mM Tris, pH8.0, 150mM NaCl, 10% glycerol, 1 % Sarkosyl. |
Storage | Store at -80°C. |
Stability | Stable for 12 months from the date of receipt of the product under proper storage and handling conditions. Avoid repeated freeze-thaw cycles. |
Reference Data | |
RefSeq | NP_078941 |
Locus ID | 79718 |
UniProt ID | Q9BZK7 |
Cytogenetics | 3q26.32 |
Refseq Size | 6550 |
Refseq ORF | 1542 |
Synonyms | C21; DC42; IRA1; MRD41; TBLR1 |
Summary | This gene is a member of the WD40 repeat-containing gene family and shares sequence similarity with transducin (beta)-like 1X-linked (TBL1X). The protein encoded by this gene is thought to be a component of both nuclear receptor corepressor (N-CoR) and histone deacetylase 3 (HDAC 3) complexes, and is required for transcriptional activation by a variety of transcription factors. Mutations in these gene have been associated with some autism spectrum disorders, and one finding suggests that haploinsufficiency of this gene may be a cause of intellectual disability with dysmorphism. Mutations in this gene as well as recurrent translocations involving this gene have also been observed in some tumors. [provided by RefSeq, Mar 2016] |
Protein Families | Druggable Genome, Transcription Factors |
Protein Pathways | Wnt signaling pathway |
Documents
FAQs |
Resources
Recombinant Protein Resources |
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