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MAB13446

Sigma-Aldrich

Anti-TIMP-2 Antibody, clone 2TMP05

clone 2TMP05, Chemicon®, from mouse

Synonym(s):

Tissue Inhibitor of Metalloproteinase-2

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About This Item

UNSPSC Code:
12352203
eCl@ss:
32160702
NACRES:
NA.41

biological source

mouse

Quality Level

antibody form

purified antibody

antibody product type

primary antibodies

clone

2TMP05, monoclonal

species reactivity

human, mouse, bovine, guinea pig, rabbit, rat

manufacturer/tradename

Chemicon®

technique(s)

immunohistochemistry: suitable (paraffin)
western blot: suitable

NCBI accession no.

UniProt accession no.

shipped in

wet ice

target post-translational modification

unmodified

Gene Information

human ... TIMP2(7077)

Specificity

MAB13446 recognizes a protein of 21kDa, identified as tissue inhibitor of metalloproteinase-2 (TIMP-2). TIMP-2 is closely related to TIMP-1 and shows the highest binding affinity to both the latent (pro) and active forms of 72kDa Type IV collagenase (also known as MMP-2 or gelatinase A). It also has affinity for the active form of 92kDa Type IV collagenase (also known as MMP-9 or gelatinase B). TIMP-2 inhibits the proteolytic invasiveness of tumor cells and normal placental trophoblast cells. CHEMICON MAB13446 may be used to evaluate the invasive nature of some tumor types and determine the tissue distribution of TIMPs in other tumors such as adenomas and also its normal tissue.

CELLULAR LOCALIZATION:

Cytoplasmic

Immunogen

A synthetic peptide from the N-terminal region of human TIMP-2 protein.

Application

Detect TIMP-2 using this Anti-TIMP-2 Antibody, clone 2TMP05 validated for use in WB, IH(P).
Immunohistology (formalin/paraffin only): 2-4μg/ml 30 min at RT.

Western blotting: 1μg/ml for 2 hrs at RT.

(Staining of formalin-fixed tissues REQUIRES boiling tissue sections in 10mM citrate buffer, pH 6.0 for 10-20 min. followed by cooling at RT for 20 min).

The optimal dilution for a specific application under a given set of experimental conditions should be determined by the investigator.
Research Category
Cell Structure
Research Sub Category
MMPs & TIMPs

Linkage

Replaces: MAB13448

Physical form

Format: Purified
Purified from ascites fluid by Protein A chromatography. 10mM PBS, pH 7.4, with 0.2% BSA and 0.09% sodium azide.

Storage and Stability

Antibody with sodium azide is stable for 12 months after date of receipt when stored at 2-8°C.

Analysis Note

Control
POSITIVE CONTROL:

Pancreatic or colon carcinoma

Other Notes

Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.

Legal Information

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Davide Visigalli et al.
BMC cancer, 9, 59-59 (2009-02-20)
The COOH terminal peptide of Pro-collagen type I (PICP, also called C3) is chemotactic for endothelial melanoma and breast cancer cells. PICP induces the expression of Metalloproteinases-2 and -9, of Vascular endothelial growth factor and of the chemokine CXCL-12 receptor
Feng-Cheng Pai et al.
Cells, 10(10) (2021-10-24)
Malignant glioma is one of the most lethal cancers with rapid progression, high recurrence, and poor prognosis in the central nervous system. Fatty acid-binding protein 6 (FABP6) is a bile acid carrier protein that is overexpressed in colorectal cancer. This
Jaqueline J Muniz et al.
Canadian journal of physiology and pharmacology, 96(3), 266-274 (2017-08-19)
We evaluated the effects of ethanol consumption on the mitogen-activated protein kinases (MAPK) and metalloproteinases (MMP) pathways in the rat cavernosal smooth muscle (CSM). Male Wistar rats were treated with ethanol (20% v/v) for 6 weeks. Quantitative real-time polymerase chain
Repeated autologous bone marrow-derived mesenchymal stem cell injections improve radiation-induced proctitis in pigs.
Linard, C; Busson, E; Holler, V; Strup-Perrot, C; Lacave-Lapalun, JV; Lhomme, B; Prat et al.
Stem Cells Translational Medicine null
Histological, histochemical, and protein changes after induced malocclusion by occlusion alteration of Wistar rats.
Guerra, Cde S; Carla Lara Pereira, Y; Issa, JP; Luiz, KG; Guimar?es, EA; Gerlach, RF; Iyomasa, MM
BioMed Research International null

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