KLHDC7B, also known as Kelch Domain Containing 7B, is a protein encoded by the KLHDC7B gene in humans. The protein belongs to the Kelch repeat superfamily, which is characterized by a sequence motif known as the Kelch repeat. These repeats form a β-propeller structure that is often involved in protein-protein interactions. Kelch domain-containing proteins play diverse roles in cellular functions, such as cytoskeleton organization, cellular morphology, and signal transduction.The specific function of KLHDC7B remains relatively uncharacterized compared to other well-studied members of the Kelch family. However, its structural features suggest that it may be involved in similar biological processes or pathways. The β-propeller structure of the Kelch domain is known to mediate interactions with various cellular components, implicating a potential role for KLHDC7B in assembling protein complexes or facilitating communication within the cell.
Research into KLHDC7B and other Kelch proteins often involves studying their expression patterns across different tissues and developmental stages, identifying the proteins they interact with, and elucidating their roles in the context of cellular signaling pathways. Advanced techniques, such as yeast two-hybrid screening, co-immunoprecipitation, and mass spectrometry, are commonly employed to uncover the molecular partners and biological functions of Kelch proteins.Understanding the role of KLHDC7B could provide insights into the regulation of the cytoskeleton, cell adhesion, and other cellular processes that rely on protein scaffolding and signaling.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Chloroquine | 54-05-7 | sc-507304 | 250 mg | $68.00 | 2 | |
Autophagy inhibitor, potentially affecting cellular pathways linked to KLHDC7B. | ||||||
Nocodazole | 31430-18-9 | sc-3518B sc-3518 sc-3518C sc-3518A | 5 mg 10 mg 25 mg 50 mg | $58.00 $83.00 $140.00 $242.00 | 38 | |
Disrupts microtubule polymerization, affecting cell cycle and potentially KLHDC7B-related pathways. | ||||||