CTSD Antibody
Mouse Monoclonal Antibody (Mab)
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Application ![]()
| WB, IHC-P, E |
---|---|
Primary Accession | P07339 |
Reactivity | Human |
Host | Mouse |
Clonality | Monoclonal |
Isotype | IgG1 |
Clone Names | 892CT11.1.1 |
Calculated MW | 44552 Da |
Gene ID | 1509 |
---|---|
Other Names | Cathepsin D, Cathepsin D light chain, Cathepsin D heavy chain, CTSD, CPSD |
Target/Specificity | Purified His-tagged CTSD protein was used to produced this monoclonal antibody. |
Dilution | WB~~1:2000 IHC-P~~1:100~500 E~~Use at an assay dependent concentration. |
Format | Purified monoclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein G column, followed by dialysis against PBS. |
Storage | Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. |
Precautions | CTSD Antibody is for research use only and not for use in diagnostic or therapeutic procedures. |
Name | CTSD |
---|---|
Synonyms | CPSD |
Function | Acid protease active in intracellular protein breakdown. Plays a role in APP processing following cleavage and activation by ADAM30 which leads to APP degradation (PubMed:27333034). Involved in the pathogenesis of several diseases such as breast cancer and possibly Alzheimer disease. |
Cellular Location | Lysosome. Melanosome. Secreted, extracellular space. Note=Identified by mass spectrometry in melanosome fractions from stage I to stage IV. In aortic samples, detected as an extracellular protein loosely bound to the matrix (PubMed:20551380) |
Tissue Location | Expressed in the aorta extracellular space (at protein level) (PubMed:20551380). Expressed in liver (at protein level) (PubMed:1426530). |
For Research Use Only. Not For Use In Diagnostic Procedures.

Provided below are standard protocols that you may find useful for product applications.
BACKGROUND
Acid protease active in intracellular protein breakdown. Involved in the pathogenesis of several diseases such as breast cancer and possibly Alzheimer disease.
REFERENCES
Burkard T.R., et al. BMC Syst. Biol. 5:17-17(2011).
Faust P.L., et al. Proc. Natl. Acad. Sci. U.S.A. 82:4910-4914(1985).
Westley B.R., et al. Nucleic Acids Res. 15:3773-3786(1987).
Redecker B., et al. DNA Cell Biol. 10:423-431(1991).
Ebert L., et al. Submitted (JUN-2004) to the EMBL/GenBank/DDBJ databases.

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