Overview
- Product nameAnti-Cathepsin B antibodySee all Cathepsin B primary antibodies ...
- DescriptionRabbit polyclonal to Cathepsin B
- Tested applicationsICC/IF, WB more details
- Species reactivityReacts with: Human
Predicted to work with: Orangutan - Immunogen
Synthetic peptide derived from within residues 200 - 300 of Human Cathepsin B.
Synthetic peptide of Human Cathepsin B.
- Positive controlThis antibody gave a positive signal in the following lysates: Human Liver Tissue; Human Kidney Tissue; Human Brain Tissue; Human Placenta Tissue; HepG2 Whole Cell; HEK293 Whole Cell Lysate.
Properties
- FormLiquid
- Storage instructionsStore at +4°C short term (1-2 weeks). Aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
- Storage bufferPreservative: 0.02% Sodium Azide
Constituents: 1% BSA, PBS, pH 7.4 -
Concentration information loading... - PurityImmunogen affinity purified
- Clonality Polyclonal
- IsotypeIgG
- Research Areas
Applications
Our Abpromise guarantee covers the use of ab92955 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
| Application | Notes |
|---|---|
| ICC/IF | ICC/IF: Use a concentration of 1 µg/ml. |
| WB | WB: Use a concentration of 1 µg/ml. Detects a band of approximately 30, 25 kDa (predicted molecular weight: 38 kDa). |
Target
- FunctionThiol protease which is believed to participate in intracellular degradation and turnover of proteins. Has also been implicated in tumor invasion and metastasis.
- Sequence similaritiesBelongs to the peptidase C1 family.
- Cellular localizationLysosome. Melanosome. Identified by mass spectrometry in melanosome fractions from stage I to stage IV.
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Database links
- Entrez Gene: 1508 Human
- Omim: 116810 Human
- SwissProt: P07858 Human
- Unigene: 520898 Human
Target information above from: UniProt accession
P07858
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010)
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Alternative names
- Amyloid precursor protein secretase antibodyAPP secretase antibodyAPPS antibody
- CATB_HUMAN antibodyCathepsin B heavy chain antibodyCathepsin B1 antibodyCathepsinB antibodyCPSB antibodyCTSB antibodycysteine protease antibodyOTTHUMP00000116009 antibodyOTTHUMP00000229510 antibodyOTTHUMP00000229511 antibodyOTTHUMP00000229512 antibodyOTTHUMP00000229514 antibodyOTTHUMP00000229515 antibodyOTTHUMP00000229516 antibodyPreprocathepsin B antibody
see all
Anti-Cathepsin B antibody images
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All lanes : Anti-Cathepsin B antibody (ab92955) at 1 µg/ml
Lane 1 :Liver (Human) Tissue Lysate - adult normal tissue (ab29889)
Lane 2 :Kidney (Human) Tissue Lysate - adult normal tissue (ab30203)
Lane 3 :Brain (Human) Tissue Lysate - adult normal tissue (ab29466)
Lane 4 :Placenta (Human) Tissue Lysate - adult normal tissue (ab29745)
Lane 5 : HepG2 (Human hepatocellular liver carcinoma cell line) Whole Cell Lysate
Lane 6 : HEK293 (Human embryonic kidney cell line) Whole Cell Lysate
Lysates/proteins at 10 µg per lane.
Secondary
Goat polyclonal Secondary Antibody to Rabbit IgG - H&L (HRP), pre-adsorbed (ab97080) at 1/5000 dilution
developed using the ECL technique
Performed under reducing conditions.
Predicted band size : 38 kDa
Observed band size : 25,30 kDa (why is the actual band size different from the predicted?)
Exposure time : 30 seconds -
ICC/IF image of ab92955 stained HepG2 cells. The cells were 100% methanol fixed (5 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody ab92955 at 1µg/ml overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti- rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
References for Anti-Cathepsin B antibody (ab92955)
ab92955 has not yet been referenced specifically in any publications.

