Src-associated in mitosis 68 kDa protein (Sam68/KHDR1) or K homology (KH) domain-containing, RNA binding, signal transduction associated 1 (KHDRBS1) is a member of the signal transducer and activator of RNA (STAR) family of RNA-binding proteins. This protein contains a KH (hnRNP K homology) RNA-binding domain located within a larger domain of 200 amino acids with RNA binding activity named GSG (GRP33/Sam68/GLD-1) domain. The Sam68 gene is mapped to human chromosome 1p35.
Specificity
Anti-Sam68 (N-terminal) recognizes human Sam68.
Application
Anti-Sam68 (N-terminal) antibody produced in rabbit may be used in immunoblotting.
Biochem/physiol Actions
Src-associated in mitosis 68 kDa protein (Sam68/KHDR1/KHDRBS1) participates in signal transduction, RNA metabolism, apoptosis, transcription, cell cycle, and regulation. Besides binding to RNA and its modulator proteins, Sam68 contains proline-rich motifs and multiple potential tyrosine phosphorylation sites that are involved in the binding to proteins with Src homology 3 (SH3) and SH2 domains. It controls the activation of nuclear transcription factor kappa B (NF-κB).
Physical form
Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.
Storage and Stability
Store at –20 °C. For continuous use, the product may be stored at 2–8 °C for up to one month. For extended storage, freeze in working aliquots at –20 °C. Repeated freezing and thawing is not recommended. Storage in “frost-free” freezers is also not recommended. If slight turbidity occurs upon prolonged storage, clarify the solution by centrifugation before use. Working dilutions should be discarded if not used within 12 hours.
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Molecular medicine reports, 20(4), 3728-3734 (2019-09-06)
Hyperglycemia promotes podocyte apoptosis and contributes to the pathogenesis of diabetic nephropathy (DN). However, the mechanisms of hyperglycemia‑induced podocyte apoptosis remain unknown. Recent studies have implicated Src‑associated substrate during mitosis of 68 kDa (Sam68) in various cellular processes including RNA metabolism
Human molecular genetics, 23(10), 2618-2628 (2014-01-10)
A significant proportion (up to 62%) of oral squamous cell carcinomas (OSCCs) may arise from oral potential malignant lesions (OPMLs), such as leukoplakia. Patient outcomes may thus be improved through detection of lesions at a risk for malignant transformation, by
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