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Key Specifications Table
Species Reactivity | Key Applications | Host | Format | Antibody Type |
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H, M | WB | Rb | Purified | Polyclonal Antibody |
Description | |
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Catalogue Number | 06-554 |
Brand Family | Upstate |
Trade Name |
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Description | Anti-STAT5B Antibody |
Product Information | |
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Format | Purified |
Presentation | 0.1M Tris-Glycine, pH 7.4, 0.15M NaCl containing 0.05% sodium azide |
Quality Level | MQ100 |
Applications | |
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Application | Anti-STAT5B Antibody is a Rabbit Polyclonal Antibody for detection of STAT5B also known as signal transducer & activator of transcription 5B & has been tested in WB. |
Key Applications |
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Biological Information | |
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Immunogen | amino acids 774-787 of human STAT5B (CGRPMDSQWIPHAQS) |
Host | Rabbit |
Specificity | STAT5B |
Isotype | IgG |
Species Reactivity |
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Antibody Type | Polyclonal Antibody |
Entrez Gene Number |
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Entrez Gene Summary | The protein encoded by this gene is a member of the STAT family of transcription factors. In response to cytokines and growth factors, STAT family members are phosphorylated by the receptor associated kinases, and then form homo- or heterodimers that translocate to the cell nucleus where they act as transcription activators. This protein mediates the signal transduction triggered by various cell ligands, such as IL2, IL4, CSF1, and different growth hormones. It has been shown to be involved in diverse biological processes, such as TCR signaling, apoptosis, adult mammary gland development, and sexual dimorphism of liver gene expression. This gene was found to fuse to retinoic acid receptor-alpha (RARA) gene in a small subset of acute promyelocytic leukemias (APLL). The dysregulation of the signaling pathways mediated by this protein may be the cause of the APLL. |
Gene Symbol |
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Purification Method | Protein A chromatography |
UniProt Number |
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UniProt Summary | FUNCTION: SwissProt: P51692 # Carries out a dual function: signal transduction and activation of transcription. Binds to the GAS element and activates PRL-induced transcription. SIZE: 787 amino acids; 89866 Da SUBUNIT: Forms a homodimer or a heterodimer with a related family member. Binds NR3C1 (By similarity). Interacts with NCOA1, NMI and SOCS7. SUBCELLULAR LOCATION: Cytoplasm (By similarity). Nucleus (By similarity). Note=Translocated into the nucleus in response to phosphorylation (By similarity). PTM: Tyrosine phosphorylated (By similarity). DISEASE: SwissProt: P51692 # Defects in STAT5B are the cause of Laron type dwarfism II (LTD2) [MIM:245590]; also known as Laron syndrome type II or Laron syndrome due to a post-receptor defect. The phenotypic features are consistent with growth hormone deficiency in the presence of normal to elevated circulating concentrations of growth hormone, and resistance to hexogeneous hormone therapy. SIMILARITY: SwissProt: P51692 ## Belongs to the transcription factor STAT family. & Contains 1 SH2 domain. |
Molecular Weight | 90-92kDa |
Product Usage Statements | |
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Quality Assurance | routinely evaluated by immunoblot on mouse 3T3/A31 or human A431 cell lysates |
Usage Statement |
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Storage and Shipping Information | |
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Storage Conditions | 2 years at -20°C |
Packaging Information | |
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Material Size | 200 µg |