ARG66618
anti-GTF2IRD1 antibody
anti-GTF2IRD1 antibody for IHC-Formalin-fixed paraffin-embedded sections,Western blot and Human
Overview
Product Description | Rabbit Polyclonal antibody recognizes GTF2IRD1 |
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Tested Reactivity | Hu |
Tested Application | IHC-P, WB |
Host | Rabbit |
Clonality | Polyclonal |
Isotype | IgG |
Target Name | GTF2IRD1 |
Antigen Species | Human |
Immunogen | KLH-conjugated synthetic peptide around the N-terminal region of Human GTF2IRD1. |
Conjugation | Un-conjugated |
Alternate Names | WBSCR11; RBAP2; WBSCR12; BEN; WBS; Williams-Beuren syndrome chromosomal region 11 protein; Williams-Beuren syndrome chromosomal region 12 protein; GTF2I repeat domain-containing protein 1; Slow-muscle-fiber enhancer-binding protein; MUSTRD1; USE B1-binding protein; General transcription factor II-I repeat domain-containing protein 1; GTF3; CREAM1; MusTRD1/BEN; hMusTRD1alpha1; General transcription factor III; Muscle TFII-I repeat domain-containing protein 1 |
Application Instructions
Application Suggestion |
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Application Note | IHC-P: Antigen Retrieval: Heat mediation was performed in Sodium citrate buffer (pH 6.0). * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist. |
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Observed Size | ~ 110 kDa |
Properties
Form | Liquid |
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Purification | Affinity purified. |
Buffer | PBS (pH 7.3), 0.02% Sodium azide and 0.2% BSA. |
Preservative | 0.02% Sodium azide |
Stabilizer | 0.2% BSA |
Storage Instruction | For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use. |
Note | For laboratory research only, not for drug, diagnostic or other use. |
Bioinformation
Database Links |
Swiss-port # Q9UHL9 Human General transcription factor II-I repeat domain-containing protein 1 |
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Gene Symbol | GTF2IRD1 |
Gene Full Name | GTF2I repeat domain containing 1 |
Background | The protein encoded by this gene contains five GTF2I-like repeats and each repeat possesses a potential helix-loop-helix (HLH) motif. It may have the ability to interact with other HLH-proteins and function as a transcription factor or as a positive transcriptional regulator under the control of Retinoblastoma protein. This gene plays a role in craniofacial and cognitive development and mutations have been associated with Williams-Beuren syndrome, a multisystem developmental disorder caused by deletion of multiple genes at 7q11.23. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2010] |
Function | May be a transcription regulator involved in cell-cycle progression and skeletal muscle differentiation. May repress GTF2I transcriptional functions, by preventing its nuclear residency, or by inhibiting its transcriptional activation. May contribute to slow-twitch fiber type specificity during myogenesis and in regenerating muscles. Binds troponin I slow-muscle fiber enhancer (USE B1). Binds specifically and with high affinity to the EFG sequences derived from the early enhancer of HOXC8 (By similarity). [UniProt] |
Cellular Localization | Nucleus. [UniProt] |
Calculated MW | 106 kDa |