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Merck
CN

AB2036

Anti-Collagen Type II Antibody

Chemicon®, from rabbit

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About This Item

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

Anti-Collagen Type II Antibody, Chemicon®, from rabbit

biological source

rabbit

antibody form

purified immunoglobulin

antibody product type

primary antibodies

clone

polyclonal

species reactivity

rat

manufacturer/tradename

Chemicon®

technique(s)

ELISA: suitable
immunohistochemistry (formalin-fixed, paraffin-embedded sections): suitable
radioimmunoassay: suitable

UniProt accession no.

shipped in

dry ice

target post-translational modification

unmodified

Gene Information

rat ... Col2A1(25412)

Application

Immunohistochemistry: 1:40 dilution for immunofluorescent staining of frozen rat articular cartilage tissue. The antibody is also reactive on paraffin embedded rat cartilage tissues at a dilution of 1:250 using an ABC detection system.

Radioimmunoassay

ELISA: 1:100-1:200

Optimal working dilutions must be determined by end user.
Research Category
Cell Structure
Research Sub Category
ECM Proteins
This Anti-Collagen Type II Antibody is validated for use in ELISA, RIA, IH, IH(P) for the detection of Collagen Type II.

Biochem/physiol Actions

Rat type II Collagen. The antibody shows less than 0.1% reactivity with rat Collagen Types I, III, V, rat Elastin and Fibronectin.

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.

Immunogen

Collagen Type II extracted and purified from rat fetal cartilage.

Physical form

Format: Purified
IgG fraction. Liquid at 1.0 mg/mL in 0.01M phosphate, 0.09M NaCl, pH 7.2

Preparation Note

Maintain frozen at -20°C for up to 6 months after date of receipt. Avoid repeated freeze/thaw cycles.

Legal Information

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

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Storage Class

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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Olimpia Ortiz-Arrabal et al.
Biomedicines, 9(7) (2021-08-07)
Because cartilage has limited regenerative capability, a fully efficient advanced therapy medicinal product is needed to treat severe cartilage damage. We evaluated a novel biomaterial obtained by decellularizing sturgeon chondral endoskeleton tissue for use in cartilage tissue engineering. In silico
Yorikazu Akatsu et al.
Cell and tissue research, 375(2), 425-435 (2018-09-28)
The objectives of this study are (1) to examine age-dependent longitudinal differences in histological responses after creation of partial-thickness articular cartilage defects (PTCDs) in rats and to use this model (2) to objectively evaluate the effectiveness of interventions for cartilage
Ana Belén Bonhome-Espinosa et al.
Journal of the mechanical behavior of biomedical materials, 104, 103619-103619 (2020-03-17)
The encapsulation of cells into biopolymer matrices enables the preparation of engineered substitute tissues. Here we report the generation of novel 3D magnetic biomaterials by encapsulation of magnetic nanoparticles and human hyaline chondrocytes within fibrin-agarose hydrogels, with potential use as
Li Zou et al.
Scientific reports, 6, 22868-22868 (2016-03-17)
Human pluripotent stem cells provide a standardized resource for bone repair. However, criteria to determine which exogenous cells best heal orthopedic injuries remain poorly defined. We evaluated osteogenic progenitor cells derived from both human embryonic stem cells (hESCs) and induced
David Sánchez-Porras et al.
Biomedicines, 9(3) (2021-04-04)
Considering the high prevalence of cartilage-associated pathologies, low self-repair capacity and limitations of current repair techniques, tissue engineering (TE) strategies have emerged as a promising alternative in this field. Three-dimensional culture techniques have gained attention in recent years, showing their

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