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Merck
CN

SAB5300375

Monoclonal Anti-SMAD4 antibody produced in mouse

clone 4G1C6, ascites fluid

别名:

DPC4, JIP, MADH4, SMAD4

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关于此项目

NACRES:
NA.41
UNSPSC Code:
12352203
Conjugate:
unconjugated
Clone:
4G1C6, monoclonal
Application:
ELISA (d), FACS, IF, IHC, WB
Citations:
1
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biological source

mouse

Quality Level

conjugate

unconjugated

antibody form

ascites fluid

antibody product type

primary antibodies

clone

4G1C6, monoclonal

mol wt

65 kDa

species reactivity

human

technique(s)

direct ELISA: 1:10,000, flow cytometry: 1:200-1:400, immunohistochemistry: 1:200-1:1,000, indirect immunofluorescence: 1:200-1:1,000, western blot: 1:500-1:2,000

isotype

IgG1

NCBI accession no.

UniProt accession no.

shipped in

wet ice

storage temp.

−20°C

target post-translational modification

unmodified

Gene Information

human ... SMAD4(4089)

Immunogen

Purified recombinant fragment of human SMAD4 expressed in E.coli.
Mouse monoclonal antibody raised against SMAD4

Physical form

Ascitic fluid containing 0.03% sodium azide.

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.


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存储类别

10 - Combustible liquids

wgk

WGK 3

法规信息

常规特殊物品
动物来源生物产品

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Pasquale Piccolo et al.
European journal of human genetics : EJHG, 22(8), 988-994 (2014-01-09)
Myhre syndrome (MS, MIM 139210) is a connective tissue disorder that presents with short stature, short hands and feet, facial dysmorphic features, muscle hypertrophy, thickened skin, and deafness. Recurrent missense mutations in SMAD4 encoding for a transducer mediating transforming growth



全球贸易项目编号

货号GTIN
SAB5300375-100UL04061837600487