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Merck

T1327

Tissue Inhibitor of Metalloproteinase-3 human

recombinant, expressed in NSO cells, >95% (SDS-PAGE)

Synonym(s):

TIMP-3

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10 μG

€713.00

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About This Item

UNSPSC Code:
12352202
NACRES:
NA.32
MDL number:

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Product Name

Tissue Inhibitor of Metalloproteinase-3 human, recombinant, expressed in NSO cells, >95% (SDS-PAGE)

biological source

human

recombinant

expressed in NSO cells

assay

>95% (SDS-PAGE)

form

lyophilized powder

mol wt

apparent mol wt ~30 kDa

technique(s)

inhibition assay: suitable

UniProt accession no.

storage temp.

−20°C

Quality Level

Gene Information

human ... TIMP3(7078)

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SRP6445SRP3174SRP3173
technique(s)

inhibition assay: suitable

technique(s)

-

technique(s)

cell culture | mammalian: suitable

technique(s)

cell culture | mammalian: suitable

recombinant

expressed in NSO cells

recombinant

expressed in HEK 293 cells

recombinant

expressed in E. coli

recombinant

expressed in E. coli

biological source

human

biological source

human

biological source

human

biological source

human

assay

>95% (SDS-PAGE)

assay

≥95% (SDS-PAGE)

assay

≥95% (HPLC), ≥95% (SDS-PAGE)

assay

≥95% (HPLC), ≥95% (SDS-PAGE)

form

lyophilized powder

form

lyophilized

form

lyophilized

form

lyophilized

mol wt

apparent mol wt ~30 kDa

mol wt

calculated mol wt 24 kDa, observed mol wt 28-32 kDa by SDS-PAGE (DTT-reduced.)

mol wt

21.8 kDa

mol wt

20.6 kDa

Analysis Note

The biological activity is measured by its ability to inhibit human MMP-2 hydrolysis of a peptide substrate.

Biochem/physiol Actions

The TIMPs are endogenous inhibitors of the matrix metalloproteinases (MMPs). TIMP-3 inhibits ADAM-17 (TACE) at nanomolar concentrations and also inhibits other metalloproteinases (sheddases) that mediate the shedding of soluble receptors and other proteins from the surface of cells.
Tissue inhibitor of metalloproteinases 3 (TIMP3) is a matrix metalloproteinase inhibitor.[1] TIMP proteins comprise the N-terminal region, which aids in the matrix metalloproteinase interaction. The C-terminal region is crucial for extracellular matrix (ECM) interaction.[2] Elevated expression of TIMP3 favors apoptosis in cancer types.[1] Its interaction with the vascular endothelial growth factor (VEGFR-2) leads to the regulation of angiogenesis.[3] TIMP3 also aids in protection against ultra-violet (UV)-induced cellular responses.[1] Missense mutations in the TIMP3 gene are implicated in Sorsby′s fundus dystrophy (SFD).[3] Mutations in the TIMP3 gene also leads to increased accumulation of the protein resulting in the thickening of the Bruch membrane. This, in turn, reduces membrane permeability towards nutrients and metabolites.[2]

General description

Tissue inhibitor of metalloproteinases 3 (TIMP3) is localized in the extracellular matrix (ECM) of epithelial cells associated with kidneys, eyes and lungs.[3] It is majorly secreted in retinal pigment epithelium (RPE).[2] TIMP3 gene is mapped to human chromosome 22q12.3[3] and is a CLOCK-dependent diurnal gene.[1] TIMP proteins display a three-lobed structure and have conserved cysteine residues.[2]

Physical form

Lyophilized from a 0.2 μm filtered solution in 25 mM Tris and 0.15 M sodium chloride, pH 7.5.

Storage Class

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Daniel Ardeljan et al.
European journal of human genetics : EJHG, 21(10), 1152-1157 (2013-02-21)
Age-related macular degeneration (AMD) is a leading cause of irreversible central visual loss in the elderly. A recent genome-wide association studies (GWAS) reported that rs9621532 near the tissue inhibitor of metalloproteinase 3 (TIMP3)/synapsin III (SYN3) region of 22q12.3 is associated
Ruth Appeltant et al.
Animal science journal = Nihon chikusan Gakkaiho, 88(9), 1279-1290 (2017-01-27)
In vitro maturation (IVM) in serum causes hampered expansion of porcine cumulus-oocyte complexes (COCs) due to excessive alpha
Sunyoung Park et al.
International journal of molecular sciences, 20(4) (2019-02-20)
The human skin is the outermost physical barrier and has its own circadian machinery that works either cooperatively with the central clock, or autonomously. Circadian rhythms have been observed in many functions related to epidermal homeostasis including hydration and inflammation
Han-Li Huang et al.
Theranostics, 9(22), 6676-6689 (2019-10-08)
Tissue inhibitors of metalloproteinase 3 (TIMP3) are a major endogenous inhibitor of matrix metalloproteinase (MMPs) that inhibit tumor growth, invasion, metastasis and angiogenesis. In this study, we found that TIMP3 expression is associated with positive prognosis of colorectal cancer (CRC)
Sarah Naessens et al.
Human mutation, 40(5), 539-551 (2019-01-23)
Sorsby fundus dystrophy (SFD) is a macular degeneration caused by mutations in TIMP3, the majority of which introduce a novel cysteine. However, the exact molecular mechanisms underlying SFD remain unknown. We aimed to provide novel insights into the functional consequences

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