Anti-HSP40, Hdj1 Antibody [3B9.E6]

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SKU:
STMA00026
Antibody Type:
Monoclonal
Applications:
WB
Applications:
IHC
Applications:
ICC/IF
Applications:
IP
Applications:
ELISA
Reactivity:
Human
Reactivity:
Mouse
Reactivity:
Rat
Host Species:
Mouse
Isotype:
IgG1
  • Immunocytochemistry/Immunofluorescence analysis using Mouse Anti-Hsp40 Monoclonal Antibody, Clone 3B9.E6 (STMA00026). Tissue: HaCaT cells. Species: Human. Fixation: Cold 100% methanol for 10 minutes at -20°C. Primary Antibody: Mouse Anti-Hsp40 Monoclonal Antibody (STMA00026) at 1:100 for 1 hour at RT. Secondary Antibody: FITC Goat Anti-Mouse (green) at 1:50 for 1 hour at RT.
  • Western Blot analysis of Human Cell lysates showing detection of Hsp40 protein using Mouse Anti-Hsp40 Monoclonal Antibody, Clone 3B9.E6 (STMA00026). Load: 15 µg. Block: 1.5% BSA for 30 minutes at RT. Primary Antibody: Mouse Anti-Hsp40 Monoclonal Antibody (STMA00026) at 1:1000 for 2 hours at RT. Secondary Antibody: Sheep Anti-Mouse IgG: HRP for 1 hour at RT.
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Description

HSP40, Hdj1 Antibody [3B9.E6]

HSP40, Hdj1 Antibody [3B9.E6] is a mouse monoclonal antibody directed against HSP40, Hdj1, offered by Assay Genie for research applications. Reported applications include WB, IHC, ICC/IF, IP and ELISA. Reported reactivity: Human, Mouse and Rat. Supplied as IgG1, purified by Protein G.

HSP40 proteins, also known as DnaJ homologs, form a large and diverse family of molecular co-chaperones defined by the presence of a conserved J-domain, typically located within the first 75 N-terminal amino acids. This domain is separated from the C-terminal region by a glycine/phenylalanine-rich linker and is critical for stimulating the ATPase activity of HSP70, thereby enhancing its ability to refold misfolded or aggregated proteins. Members of the HSP40 family, including the well-characterized Hdj1, are involved in a wide range of cellular processes such as protein folding, translocation, degradation, and the assembly of multi-protein complexes. In the nervous system, these functions are vital for maintaining proteostasis, especially under stress conditions that promote protein misfolding—a hallmark of neurodegenerative diseases like Alzheimer’s, Parkinson’s, and Huntington’s disease. HSP40-HSP70 complexes form the core of a larger chaperone network, interacting with co-factors such as Hip, Hop, HSP90, CHIP, and BAG-1 to direct client proteins toward refolding or degradation pathways. Differences among HSP40 subtypes, such as the presence of a zinc finger domain in HDJ2 and yeast Ydj1, further modulate their folding capabilities and functional specificity. Given their central role in regulating HSP70 activity and managing proteotoxic stress, HSP40 proteins are emerging as critical modulators of neuronal health and promising targets for therapeutic intervention in neurodegenerative disease research. This antibody is also available conjugated to ATTO 390, ATTO 488, ATTO 594, APC, Biotin, FITC, HRP, PerCP and RPE. Supplied in 100 µg. For research use only; not for diagnostic or therapeutic procedures.

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