Skip to content Skip to footer
0 items - $0.00 0

MMP13 (Cleaved-Tyr104) rabbit pAb

MMP13 (Cleaved-Tyr104) rabbit pAb

ENT-A15552

Description

 

 

 

REF ENT-A15552
Category Antibody Polyclonal
Description MMP13 (Cleaved-Tyr104) rabbit pAb
Source Rabbit
Applications WB;ELISA;IHC
Reactivity Human;Rat;Mouse;
Reactivity Human;Rat;Mouse;
Dilution WB 1:500-2000;IHC-p 1:50-300; ELISA 2000-20000
Immunogen Synthesized peptide derived from human MMP13 (Cleaved-Tyr104)
Storage Stability -20°C/1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Observed Band KD 42 53kD
Human Gene ID 4322
Human Swiss Prot Nº P45452
Subcellular Location Secreted, extracellular space, extracellular matrix . Secreted .

Other Name: Collagenase 3 (EC 3.4.24.-;Matrix metalloproteinase-13;MMP-13)

Background: cofactor:Binds 2 zinc ions per subunit.,cofactor:Binds 4 calcium ions per subunit.,disease:Defects in MMP13 are the cause of spondyloepimetaphyseal dysplasia type 2 (SEMD2) [MIM:602111]; also known as spondyloepimetaphyseal dysplasia type Missouri. SEMDs are a heterogeneous group of skeletal disorders characterized by defective growth and modeling of the spine and long bones. The SEMDs are distinguished from the spondylometaphyseal dysplasias and the spondyloepiphyseal dysplasias by the combined involvement of the epiphyses and metaphyses. The 3 disorders have malformations of the vertebrae in common.,domain:The conserved cysteine present in the cysteine-switch motif binds the catalytic zinc ion, thus inhibiting the enzyme. The dissociation of the cysteine from the zinc ion upon the activation-peptide release activates the enzyme.,function:Degrades collagen type I. Does not act on gelatin or casein. Could have a role in tumoral process.,similarity:Belongs to the peptidase M10A family.,similarity:Contains 4 hemopexin-like domains.,tissue specificity:Seems to be specific to breast carcinomas.,