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Catalog: YT4660
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Price
Status
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200μL
$450.00
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100μL
$280.00
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40μL
$150.00
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Main Information
Target

TIMP-3

Host Species

Rabbit

Reactivity

Human, Mouse, Rat

Applications

WB, ELISA, IHC

MW

25kD (Observed)

Conjugate/Modification


Unmodified

Detailed Information
Recommended Dilution Ratio
WB 1:500-2000; IHC 1:50-300; ELISA 1:2000-20000
Formulation
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Specificity
TIMP-3 Polyclonal Antibody detects endogenous levels of TIMP-3 protein.
Purification
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage
-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration
1 mg/ml
MW(Observed)
25kD
Modification
Unmodified
Clonality
Polyclonal
Isotype
IgG
Related Products
Primary Antibodies
TIMP-3 Polyclonal Antibody
YT4660

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ELISA Kits
Human TIMP-3 ELISA Kit
KE1168

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ELISA Kits
Total TIMP-3 Cell-Based Colorimetric ELISA Kit
KA3399C

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Secondary Antibodies
HRP* Goat Anti Mouse IgG(H+L)
RS0001

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Secondary Antibodies
HRP* Goat Anti Rabbit IgG(H+L)
RS0002

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Primary Antibodies
β-actin (PTR2364) mouse mAb
YM3028

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Primary Antibodies
GAPDH (PTR2304) mouse mAb
YM3029

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Antigen&Target Information
Immunogen:
The antiserum was produced against synthesized peptide derived from human TIMP3. AA range:91-140
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Specificity:
TIMP-3 Polyclonal Antibody detects endogenous levels of TIMP-3 protein.
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Gene Name:
TIMP3
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Protein Name:
Metalloproteinase inhibitor 3
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Other Name:
TIMP3 ;
Metalloproteinase inhibitor 3 ;
Protein MIG-5 ;
Tissue inhibitor of metalloproteinases 3 ;
TIMP-3
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Database Link:
Organism Gene ID SwissProt
Human 7078; P35625;
Mouse 21859; P39876;
Rat P48032;
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],
Function:
Disease: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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Cellular Localization:
Secreted, extracellular space, extracellular matrix.
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Tissue Expression:
Kidney,Mammary carcinoma,Pancreas,Placenta,Retina,Uterus,
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Research Areas:
>>Proteoglycans in cancer ;
>>MicroRNAs in cancer
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Catalog: YT4660
Size
Price
Status
Qty.
200μL
$450.00
In stock

0

100μL
$280.00
In stock

0

40μL
$150.00
In stock

0

Add to cart

Collected

Collect

Customized Service
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