B1814

BMP2, human

Name: BMP2, human
Brand: SIGMA
Price: 2050 PLN

Carrier Free, ≥98% (SDS-PAGE), recombinant, expressed in E. coli, lyophilized powder, suitable for cell culture

Synonim(y):

Bone Morphogenetic Protein 2 human, BMP-2

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Wybierz wielkość

10 μG

2050,00 zł

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Informacje o tej pozycji

UNSPSC Code:

12352202

NACRES:

NA.32

MDL number:

MFCD03097877

Biological source:

human

Recombinant:

expressed in E. coli

Assay:

≥98% (SDS-PAGE)

Form:

lyophilized powder

Mol wt:

26 kDa

Impurities:

Endotoxin, tested

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Nazwa produktu

Bone Morphogenetic Protein 2 human, Carrier Free, ≥98% (SDS-PAGE), recombinant, expressed in E. coli, lyophilized powder, suitable for cell culture

biological source

human

recombinant

expressed in E. coli

assay

≥98% (SDS-PAGE)

form

lyophilized powder

mol wt

26 kDa

packaging

pkg of 10 μg

storage condition

avoid repeated freeze/thaw cycles (Do not store in a frost-free freezer.)

technique(s)

cell culture | mammalian: suitable

impurities

Endotoxin, tested

color

white

solubility

water: soluble 0.100 mL, clear, colorless

UniProt accession no.

P12643

storage temp.

−20°C

Quality Level

200

Gene Information

human ... BMP2(650)

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Ta pozycja	B3555	B2805	B1434
Sigma-Aldrich B1814 Bone Morphogenetic Protein 2 human	Sigma-Aldrich B3555 Bone Morphogenetic Protein 2 human	Sigma-Aldrich B2805 Bone Morphogenetic Protein 6 human	Sigma-Aldrich B1434 Bone Morphogenetic Protein 7 human
recombinant expressed in E. coli	recombinant expressed in E. coli	recombinant expressed in NSO cells	recombinant expressed in CHO cells
technique(s) cell culture \| mammalian: suitable	technique(s) cell culture \| mammalian: suitable	technique(s) cell culture \| mammalian: suitable	technique(s) cell culture \| mammalian: suitable
biological source human	biological source human	biological source human	biological source human
assay ≥98% (SDS-PAGE)	assay ≥98% (SDS-PAGE)	assay >95% (SDS-PAGE)	assay >95% (SDS-PAGE)
Quality Level 200	Quality Level 200	Quality Level 100	Quality Level 100
form lyophilized powder	form lyophilized powder	form lyophilized powder	form lyophilized powder

Biochem/physiol Actions

Cellular responses to BMP-2 are mediated by the formation of hetero-oligomeric complexes of type I and type II serine/threonine kinase receptors. BMPs stimulate angiogenesis by inducing the production of VEGF-A by osteoblasts. Human, mouse, and rat BMP-2 demonstrate 100% homology.

Physical form

Lyophilized from a 0.2 μm filtered buffered solution.

Analysis Note

The biological activity is measured by its ability to induce alkaline phosphatase production by ATDC5 chondrogenic cells.

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Klasa składowania

11 - Combustible Solids

wgk

WGK 3

flash_point_f

104.0 °F - closed cup

flash_point_c

40.0 °C - closed cup

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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Age-Independent Cartilage Generation for Synovium-Based Autologous Chondrocyte Implantation.

Ernst B Hunziker et al.

Tissue engineering. Part A, 21(13-14), 2089-2098 (2015-04-22)

The articular cartilage layer of synovial joints is commonly lesioned by trauma or by a degenerative joint disease. Attempts to repair the damage frequently involve the performance of autologous chondrocyte implantation (ACI). Healthy cartilage must be first removed from the

Machine oil inhibits the osseointegration of orthopaedic implants by impairing osteoblast attachment and spreading.

Lindsay A Bonsignore et al.

Journal of orthopaedic research : official publication of the Orthopaedic Research Society, 33(7), 979-987 (2015-02-14)

The most important factor contributing to short-term and long-term success of cementless total joint arthroplasties is osseointegration. Osseointegration leads to a direct structural and functional connection between living bone and the surface of an implant. Surface contaminants may remain on

A pilot study of conically graded chitosan-gelatin hydrogel/PLGA scaffold with dual-delivery of TGF-β1 and BMP-2 for regeneration of cartilage-bone interface.

Fengxuan Han et al.

Journal of biomedical materials research. Part B, Applied biomaterials, 103(7), 1344-1353 (2014-11-12)

Repair of cartilage-bone interface tissue remains challenging, because it combines different cell types and gradients of composition and properties. To enable simultaneous regeneration of bone, cartilage, and especially their interface, a conically graded scaffold of chitosan-gelatin hydrogel/poly(l-lactide-co-glycolide) (PLGA) was facilely

Molecular mechanism of CHRDL1-mediated X-linked megalocornea in humans and in Xenopus model.

Thorsten Pfirrmann et al.

Human molecular genetics, 24(11), 3119-3132 (2015-02-26)

Chordin-Like 1 (CHRDL1) mutations cause non-syndromic X-linked megalocornea (XMC) characterized by enlarged anterior eye segments. Mosaic corneal degeneration, presenile cataract and secondary glaucoma are associated with XMC. Beside that CHRDL1 encodes Ventroptin, a secreted bone morphogenetic protein (BMP) antagonist, the

Effects of blockade of endogenous Gi signaling in Tie2-expressing cells on bone formation in a mouse model of heterotopic ossification.

Liping Wang et al.

Journal of orthopaedic research : official publication of the Orthopaedic Research Society, 33(8), 1212-1217 (2015-03-17)

Available evidence indicates that some Tie2-expressing (Tie2(+) ) cells serve as multipotent progenitors that have robust BMP-dependent osteogenic activity and mediate heterotopic ossification (HO). Since signaling through the G protein Gi is required for cell motility, we hypothesized that blockade

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