蛋白
抗体
检测试剂盒
蛋白MARKER
分子生物学
规格：
查看说明书TBLR1 Rabbit pAb
Cat#:DPA04208应用：WB,IHC,ICC/IF
| Product Name: | TBLR1 Rabbit pAb |
| Cat No.: | DPA04208 |
| Clonality: | Polyclonal |
| Species Reactivity: | Human, Mouse, Rat |
| Tested Applications: | WB,IHC,ICC/IF |
| Recommended Dilution: | WB: 1:2000 IHC: 1:20 ICC/IF: 1:50 |
| Size: | 30ul 50ul 100uL |
| Format: | Liquid |
| Source: | Rabbit |
| Purification Method: | Affinity Purification |
| Isotype: | IgG |
| Conjugate: | Un-conjugated |
| Storage: | Store at -20°C. Supplied in 50nM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide a |
| Immunogen: | A synthetic peptide of human TBLR1 |
| Calculated Molecular Weight: | 56 kDa |
| Observed Molecular Weight: | 56 kDa |
| GenBank Accession Number: | Q9BZK7 |
| Gene ID (NCBI): | 79718 |
| Synonyms: | C21; DC42; IRA1; MRD41; TBLR1 |
| Background: | 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] |
| Category: | Primary Ab |
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