Tripartite Motif-Containing Protein 29 (TRIM29) Antibody
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Description
Tripartite Motif-Containing Protein 29 (TRIM29) Antibody is a Rabbit polyclonal antibody for the detection of Human Tripartite Motif-Containing Protein 29 (TRIM29).
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Product specifications
| Category | Primary Antibodies |
| Immunogen Target | Tripartite Motif-Containing Protein 29 (TRIM29) |
| Host | Rabbit |
| Reactivity | Human |
| Recommended Dilution | Optimal dilutions/concentrations should be determined by the end user. |
| Clonality | Polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Size 1 | 50 µg |
| Size 2 | 100 µg |
| Form | Liquid |
| Tested Applications | ELISA, WB, IHC |
| Buffer | 0.01 M PBS, pH 7.4, 50% glycerol, 0.05% Proclin-300. |
| Availability | Shipped within 5-12 working days. |
| Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. |
| Dry Ice | No |
| UniProt ID | Q14134 |
| Gene ID | 23650 |
| NCBI Accession | NP_036233.2 |
| Background | Antibody anti-TRIM29 |
| Status | RUO |
Descripción
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Human TRIM29 (Tripartite motif-containing protein 29) ELISA Kit
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TRIM29 antibody
The protein encoded by this gene belongs to the TRIM protein family. It has multiple zinc finger motifs and a leucine zipper motif. It has been proposed to form homo- or heterodimers which are involved in nucleic acid binding. Thus, it may act as a transcriptional regulatory factor involved in carcinogenesis and/or differentiation. It may also function in the suppression of radiosensitivity since it is associated with ataxia telangiectasia phenotype.
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Tripartite Motif-Containing Protein 29 (TRIM29) Antibody
TRIM29 Antibody is a Rabbit Polyclonal antibody against TRIM29. The protein encoded by this gene belongs to the TRIM protein family. It has multiple zinc finger motifs and a leucine zipper motif. It has been proposed to form homo- or heterodimers which are involved in nucleic acid binding. Thus, it may act as a transcriptional regulatory factor involved in carcinogenesis and/or differentiation. It may also function in the suppression of radiosensitivity since it is associated with ataxia telangiectasia phenotype.
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