SKU: WR5345 Categories: ,

U-Blot® TIMP-3 Rabbit mAb

Price range: $268.00 through $328.00

SKU: WR5345-50
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Product details

Background:This gene belongs to the TIMP gene family. The proteins encoded by this gene family are inhibitors of the matrix metalloproteinases, a group of peptidases involved in degradation of the extracellular matrix (ECM). Expression of this gene is induced in response to mitogenic stimulation and this netrin domain-containing protein is localized to the ECM. Mutations in this gene have been associated with the autosomal dominant disorder Sorsby's fundus dystrophy. [provided by RefSeq, Jul 2008],

Specifications

Size50μL/100μL
TargetTIMP-3
ReactivityHuman, Mouse, Rat
ApplicationsWB, IHC, IF, ELISA
MW(Calculated)24kD
MW(Observed)20kD
Host SpeciesRabbit
IsotypeIgG,Kappa
Conjugate/ModificationUnmodified
Recommended Dilution RatioIHC 1:200-1:1000; WB 1:500-1:2000; IF 1:200-1:1000; ELISA 1:5000-1:20000; / Note: For IHC, we suggest antigen retrieval with TE buffer pH 9.0 (Cat#WT1004)
FormulationPBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
PurificationRecombinant Antibody expressed in animal component-free (ACF) media, purified via Protein A affinity chromatography.
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration
ClonalityMonoclonal
Clone NumberRM1580R
ImmunogenThe specific immunogen used to produce this antibody is proprietary information.
SpecificityEndogenous
Gene NameTIMP3
Protein NameMetalloproteinase inhibitor 3
Other NameTIMP3; / Metalloproteinase inhibitor 3; / Protein MIG-5; / Tissue inhibitor of metalloproteinases 3; / TIMP-3
SpeciesHuman
Gene ID7078
UniprotP35625,
Species.1Mouse
Gene ID.121859
Uniprot.1P39876,
Species.2Rat
Gene ID.2
Uniprot.2P48032
Cellular LocalizationSecreted, extracellular space, extracellular matrix.
Tissue ExpressionKidney,Mammary carcinoma,Pancreas,Placenta,Retina,Uterus,
Signaling_pathwayHuman Diseases >> Cancer: overview >> MicroRNAs in cancer
Research Areas>>Proteoglycans in cancer; / >>MicroRNAs in cancer
FunctionDisease: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.,Function:Complexes with metalloproteinases (such as collagenases) and irreversibly inactivates them. 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.,online information:Retina International's Scientific Newsletter,similarity:Belongs to the protease inhibitor I35 (TIMP) family.,similarity:Contains 1 NTR domain.,
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