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G5035

Sigma-Aldrich

Granulocyte-Macrophage Colony-Stimulating Factor human

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

Synonyme(s) :

GM-CSF human

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About This Item

Numéro MDL:
MFCD00166611
Code UNSPSC :
12352202
Nomenclature NACRES :
NA.77

Nom du produit

Granulocyte-Macrophage Colony-Stimulating Factor human, GM-CSF, recombinant, expressed in E. coli, suitable for cell culture

Source biologique

human

Niveau de qualité

200

Produit recombinant

expressed in E. coli

Essai

≥98% (SDS-PAGE)

Forme

lyophilized powder

Puissance

≤0.1 ng/mL EC50

Poids mol.

14.6 kDa

Conditionnement

pkg of 4X5 μg
pkg of 5 μg

Conditions de stockage

avoid repeated freeze/thaw cycles

Technique(s)

cell culture | mammalian: suitable

Impuretés

≤1.000 EU/μg

Couleur

white

Solubilité

water: soluble 0.010 mL, clear, colorless

Numéro d'accès UniProt

P04141

Température de stockage

−20°C

Informations sur le gène

human ... CSF2(1437) , CSF2(1437)

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Description générale

Package size based on protein content

Actions biochimiques/physiologiques

Granulocyte-macrophage colony stimulating factor (GM-CSF) is a growth and differentiation factor for cells in the granulocyte, macrophage and eosinophil lineage. GM-CSF stimulates colony formation from pluripotential progenitor cells at extremely low concentrations and is an essential survival and proliferative factor for hematopoietic progenitor cells in all divisions up to maturity. It also stimulates growth in some epithelial cells and osteoclasts. GM-CSF is produced by a variety of cell types (monocytes, endothelial cells, T-cells, fibroblasts, mitogen-stimulated B-cells, and LPS-stimulated macrophages). GM-CSF is secreted as a single chain glycoprotein containing 128 amino acids for human with a conserved disulfide bond. Human and murine GM-CSF share approx. 54% sequence homology and do not cross-react in bioactivity.

Forme physique

Lyophilized from a 0.2 μm filtered, 10 mM sodium citrate, pH 3.5 solution.

Remarque sur l'analyse

The proliferative activity of human GM-CSF is tested in culture using human TF-1 cells.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)

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Certificats d'analyse (COA)

Lot/Batch Number
0000321537
0000215784
049M4181V
11190123
018M4146V

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Alessio Lanna et al.
Methods in molecular biology (Clifton, N.J.), 2654, 251-261 (2023-04-28)
Eukaryotes solve the DNA-end replication problem synthesizing hexameric chromosome ends known as telomeres. Recent studies have uncovered unexpected functions of telomeres in linking synaptic signaling and vesicle transport, with at least one pathway directly involved in transferring telomeres through the
Benhur Lee et al.
Research square (2021-10-07)
Bats are significant reservoir hosts for many viruses with zoonotic potential1. SARS-CoV-2, Ebola virus, and Nipah virus are examples of such viruses that have caused deadly epidemics and pandemics when spilled over from bats into human and animal populations2,3. Careful
Satoshi Ikegame et al.
Nature microbiology, 8(6), 1108-1122 (2023-05-05)
Morbilliviruses are among the most contagious viral pathogens of mammals. Although previous metagenomic surveys have identified morbillivirus sequences in bats, full-length morbilliviruses from bats are limited. Here we characterize the myotis bat morbillivirus (MBaMV) from a bat surveillance programme in
Rongqing Pan et al.
Cell, 185(9), 1521-1538 (2022-04-22)
Interest in harnessing natural killer (NK) cells for cancer immunotherapy is rapidly growing. However, efficacy of NK cell-based immunotherapy remains limited in most trials. Strategies to augment the killing efficacy of NK cells are thus much needed. In the current
Kazuhiro Maki et al.
International journal of hematology, 100(4), 361-369 (2014-07-25)
Myelodysplastic syndrome (MDS) is a stem cell tumor characterized by dysplastic features and ineffective hematopoiesis in the early phase and leukemic progression in the late phase. Speculating that differences in the expression of genes and microRNA (miRNA) in control and
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