GTF2I Repeat Domain Containing 1 (GTF2IRD1) Antibody (FITC)

Por favor contáctenos para obtener información detallada sobre el precio y disponibilidad.
Description
GTF2IRD1 Antibody (FITC) is a Rabbit Polyclonal against GTF2IRD1.
Documents del producto
Product specifications
Category | Primary Antibodies |
Immunogen Target | GTF2I Repeat Domain Containing 1 (GTF2IRD1) |
Host | Rabbit |
Reactivity | Human |
Recommended Dilution | Optimal dilutions/concentrations should be determined by the end user. |
Clonality | Polyclonal |
Conjugation | FITC |
Isotype | IgG |
Purity | > 95% |
Purification | Purified by Protein G. |
Size 1 | 20 µg |
Size 2 | 50 µg |
Size 3 | 100 µg |
Size 4 | 200 µg |
Size 5 | 1 mg |
Form | Liquid |
Buffer | 0.01 M PBS, pH 7.4, 0.03% Proclin-300 and 50% Glycerol. |
Availability | Shipped within 5-10 working days. |
Storage | Aliquot and store at -20°C. Avoid exposure to light. Avoid repeated freeze/thaw cycles. |
Dry Ice | No |
UniProt ID | Q9UHL9 |
Gene ID | 9569 |
Background | Antibody anti-GTF2IRD1 |
Status | RUO |
Descripción
Related Products

GTF2IRD1 antibody
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).
Ver Producto
GTF2I Repeat Domain Containing 1 (GTF2IRD1) Antibody
GTF2IRD1 Antibody is a Rabbit Polyclonal antibody against GTF2IRD1. 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.
Ver Producto
GTF2I Repeat Domain Containing 1 (GTF2IRD1) Antibody
Rabbit polyclonal antibody against GTF2IRD1 protein. Immunogen region is N-terminal.
Ver Producto