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Merck
CN

D8935

Nidogen-1 (NID1) human

recombinant, expressed in HEK 293 cells, suitable for cell culture

别名:

Entactin, NID, NID-1, NID1

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关于此项目

NACRES:
NA.77
UNSPSC Code:
12352202
Form:
lyophilized powder
Assay:
95% (SDS-PAGE)
Recombinant:
expressed in HEK 293 cells
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recombinant

expressed in HEK 293 cells

assay

95% (SDS-PAGE)

form

lyophilized powder

technique(s)

cell culture | mammalian: suitable

storage temp.

−20°C

General description

Nidogen-1 belongs to the nidogens family of glycoproteins. This family consists of nidogen-1 and nidogen-2, both of which are sulfated monomeric glycoproteins. Nidogen-1 is ubiquitously present in the synaptic and extra synaptic basal lamina. It is mapped to human chromosome 1q42.3. Nidogen-1 encodes a 139 kDa, three globular domains namely G1, G2 and G3 and has multiple epidermal growth factor repeats. Recombinant human nidogen-1 is expressed in human HEK 293 cells as a glycoprotein with a calculated molecular mass of 133.5 kDa (amino acids 29-1247). This protein is manufactured in human cells, with no serum. The human cells expression system allows human-like glycosylation and folding, and often supports higher specific activity of the protein. The protein is produced with no artificial tags.

Application

This recombinant human nidogen-1 product can be used as an attachment factor for cells adherence.

Biochem/physiol Actions

Nidogen-1 (NID-1) is thought to have an important role in the construction of basement membrane by linking between the networks of laminin and collagen IV. Genetic elimination of the nidogen-1 binding site on the mouse laminin γ1 chain leads to impaired deposition of basement membranes and hampers microvessel maturation. Nidogen 1 and 2 double knockout in mouse fibroblasts led to the loss of all major basal membrane components from the epidermal-collagen interface, and complete abolishment of hemidesmosomes. Supplementation by either recombinant nidogen-1 or -2 improved basal membrane formation. Mutations in NID1and laminin γ1 is implicated in pathogenesis of Dandy-Walker spectrum disorders.

存储类别

13 - Non Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

常规特殊物品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Mutations in Extracellular Matrix Genes NID1 and LAMC1 Cause Autosomal Dominant D andy-W alker Malformation and Occipital Cephaloceles
Darbro BW, et al.
Human Mutation, 34(8), 1075-1079 (2013)
Analysis of nidogen-1/laminin gamma1 interaction by cross-linking, mass spectrometry, and computational modeling reveals multiple binding modes
Lossl P, et al.
Testing, 9(11), e112886-e112886 (2014)
Lack of nidogen-1 and-2 prevents basement membrane assembly in skin-organotypic coculture
Nischt R, et al.
The Journal of Investigative Dermatology, 127(3), 545-554 (2007)
Skin basement membrane: the foundation of epidermal integrity?BM functions and diverse roles of bridging molecules nidogen and perlecan
Breitkreutz D, et al.
BioMed Research International, 2013 (2013)
Basement Membrane Type IV Collagen and Laminin: An Overview of Their Biology and Value as Fibrosis Biomarkers of Liver Disease
Mak KM, et al.
The Anatomical Record, 300(8), 1371-1390 (2017)

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