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Anti-TIMP3 antibody [136-13H4]
See all TIMP3 products (11) ...
Mouse monoclonal [136-13H4] to TIMP3
Recognizes the ~27 kDa glycosylated and the ~24 kDa non-glycosylated forms of TIMP3. Does not cross-react with TIMP1 or TIMP2.
IHC-P, WB, IHC-Frmore details
Reacts with
Rabbit, Human, Baboon
Predicted to work with
Mouse, Horse, Xenopus laevis, Cynomolgus Monkey, Macaque Monkey
Does not react with
Rat, Chicken, Cow, Pig
Synthetic peptide: SNFGYPGYQSKHYACIRQK, corresponding to amino acids 170-188 of Human TIMP3
SNFGYPGYQS KHYACIRQK
293 or Caco-2 cells Unfixed eye tissue
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
Preservative: 0.1% Sodium Azide
Constituents: 0.1% BSA, 100mM Sodium phosphate buffer, pH 7.0
Concentration information loading...
Monoclonal
136-13H4
NS1
IgG1
Cell Biology >> Proteolysis / Ubiquitin >> Protease inhibitors >> Metalloprotease inhibitors >> TIMPs
Cancer >> Invasion/microenvironment >> ECM >> Extracellular matrix >> TIMPs
Cancer >> Invasion/microenvironment >> Angiogenesis >> ECM enzymes >> TIMPs
Neuroscience >> Sensory System >> Visual system
Signal Transduction >> Cytoskeleton / ECM >> Extracellular Matrix >> ECM Enzymes >> MMP Inhibitors
Cardiovascular >> Angiogenesis >> Adhesion / ECM >> Matrix Metalloproteinases >> TIMP
Cell Biology >> Apoptosis >> Extracellular Signals >> Granzymes
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)-TIMP3 antibody [136-13H4](ab58804)
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Our Abpromise guarantee covers the use of ab58804 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
IHC-P: 1/10Perform heat mediated antigen retrieval before commencing with IHC staining protocol.
WB: Use a concentration of 5 µg/mlPredicted molecular weight: 24 kDa.
IHC-Fr: Use a concentration of 2 - 10 µg/ml.
Is unsuitable for ,ICC/IF or IP.
Complexes with metalloproteinases (such as collagenases) and irreversibly inactivates them by binding to their catalytic zinc cofactor. May form part of a tissue-specific acute response to remodeling stimuli. Known to act on MMP-1, MMP-2, MMP-3, MMP-7, MMP-9, MMP-13, MMP-14 and MMP-15.
Defects in TIMP3 are the cause of Sorsby fundus dystrophy (SFD) [MIM:136900]. SFD is a rare autosomal dominant macular disorder with an age of onset in the fourth decade. It is characterized by loss of central vision from subretinal neovascularization and atrophy of the ocular tissues. Generally, macular disciform degeneration develops in the patients eye within 6 months to 6 years.
Belongs to the protease inhibitor I35 (TIMP) family.
Contains 1 NTR domain.
Secreted > extracellular space > extracellular matrix.
Target information above from: UniProt accessionP35625
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)-TIMP3 antibody [136-13H4](ab58804)
](/ps/datasheet/images/58/ab58804/TIMP3-Primary-antibodies-ab58804-1.jpg)
ab58804 (1µg/ml) staining TIMP3 in human placenta using an automated system (DAKO Autostainer Plus). Using this protocol there is cytoplasmic/secreted staining of syncytiotrophoblasts.
Sections were rehydrated and antigen retrieved with the Dako 3 in 1 AR buffer EDTA pH 9.0 in a DAKO PT link. Slides were peroxidase blocked in 3% H2O2 in methanol for 10 mins. They were then blocked with Dako Protein block for 10 minutes (containing casein 0.25% in PBS) then incubated with primary antibody for 20 min and detected with Dako Envision Flex amplification kit for 30 minutes. Colorimetric detection was completed with Diaminobenzidine for 5 minutes. Slides were counterstained with Haematoxylin and coverslipped under DePeX. Please note that, for manual staining, optimization of primary antibody concentration and incubation time is recommended. Signal amplification may be required.
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](/ps/datasheet/images/58/ab58804/TIMP3-Primary-antibodies-ab58804-1.jpg)
ab58804 (1µg/ml) staining TIMP3 in human placenta using an automated system (DAKO Autostainer Plus). Using this protocol there is cytoplasmic/secreted staining of syncytiotrophoblasts.
Sections were rehydrated and antigen retrieved with the Dako 3 in 1 AR buffer EDTA pH 9.0 in a DAKO PT link. Slides were peroxidase blocked in 3% H2O2 in methanol for 10 mins. They were then blocked with Dako Protein block for 10 minutes (containing casein 0.25% in PBS) then incubated with primary antibody for 20 min and detected with Dako Envision Flex amplification kit for 30 minutes. Colorimetric detection was completed with Diaminobenzidine for 5 minutes. Slides were counterstained with Haematoxylin and coverslipped under DePeX. Please note that, for manual staining, optimization of primary antibody concentration and incubation time is recommended. Signal amplification may be required.
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