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Documentos Principais

G1777

Sigma-Aldrich

Glial Cell Line-derived Neurotrophic Factor human

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

Sinônimo(s):

ATF, GDNF

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About This Item

Número CE:
Número MDL:
Código UNSPSC:
12352202
NACRES:
NA.32

fonte biológica

human

Nível de qualidade

recombinante

expressed in E. coli

Ensaio

≥98% (SDS-PAGE)

Formulário

lyophilized powder

peso molecular

~30 kDa

embalagem

pkg of 10 μg

condição de armazenamento

avoid repeated freeze/thaw cycles

técnica(s)

cell culture | mammalian: suitable

Impurezas

endotoxin, tested

cor

white

nº de adesão UniProt

temperatura de armazenamento

−20°C

Informações sobre genes

human ... GDNF(2668)

Descrição geral

Glial cell line-derived neurotrophic factor (GDNF) human gene is located on human chromosome 5p13.2.

Aplicação

Glial cell line-derived neurotrophic factor human (GDNF) has been used as a component in the neurobasal medium for neural differentiation. It has also been used for self-renewal, expansion and differentiation of spermatogonial stem cells (SSCs).

Ações bioquímicas/fisiológicas

Glial Cell Line-Derived Neurotrophic Factor is a member of the cysteine-knot superfamily of growth factors that assume stable dimeric protein structures. GDNF is founding member of the GDNF family of ligands, which to date include GDNF, neurturin (NTN), persephin (PSP) and artemin (ART). GDNF is a glycosylated disulfide-linked homodimeric protein of ~15 kDa. Mature rat and human GDNF share ~93% sequence homology, with strong species cross-reactivity. GDNF signals through a multicomponent receptor system, composed of a RET and one of the four GFRα (α1-α4) receptors. GDNF specifically promotes dopamine uptake and survival and morphological differentiation of midbrain neurons. Using the Parkinson′s disease mouse model, GDNF has been shown to improve conditions such as bradykinesia, rigidity, and postural instability. GDNF promotes survival of various neuronal cells in central and peripheral nervous systems and different stages of development, including motoneurons, midbrain dopaminergic neurons, Purkinje cells and sympathetic neurons. Cells known to express GDNF include Sertoli cells, type 1 astrocytes, Schwann cells, neurons, pinealocytes and skeletal muscle cells. In addition, exogenously applied GDNF has been shown to rescue damaged facial motor neurons in vivo.
Glial cell line-derived neurotrophic factor human (GDNF) acts as a morphogen in kidney development and modulates spermatogonial differentiation. Mutations in this gene may be associated with Hirschsprung′s disease, Tourette syndrome (TS) and attention deficit/ hyperactivity disorder (ADHD). It is used to treat Parkinson′s disease.

forma física

Lyophilized from a 0.2 μm filtered solution of 10 mM sodium citrate and 150 mM sodium chloride containing 0.5 mg bovine serum albumin.

Nota de análise

The biological activity of GDNF is determined by the dose-dependent dopamine uptake by rat ventral mesencephalic cultures.

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)


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Visite a Biblioteca de Documentos

Novel functions and signalling pathways for GDNF
Sariola H and Saarma M
Journal of Cell Science, 116(19), 3855-3862 (2003)
GDNF gene is associated with tourette syndrome in a family study
Huertas-Fernandez I, et al.
Movement Disorders, 30(8), 1115-1120 (2015)
Jacob L Roam et al.
Biomaterials, 35(24), 6473-6481 (2014-05-13)
Introduction of spatial patterning of proteins, while retaining activity and releasability, is critical for the field of regenerative medicine. Reversible binding to heparin, which many biological molecules exhibit, is one potential pathway to achieve this goal. We have covalently bound
Generation of Mouse Spermatogonial Stem-Cell-Colonies in A Non-Adherent Culture
Azizi H, et al.
Cell Journal, 19(2), 238-238 (2017)
Gain at chromosomal region 5p15. 33, containing TERT, is the most frequent genetic event in early stages of non-small cell lung cancer
Kang JU, et al.
Cancer Genetics and Cytogenetics, 182(1), 1-11 (2008)

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