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PRS4691

Sigma-Aldrich

Anti-GDF6 antibody produced in rabbit

affinity isolated antibody, buffered aqueous solution

Sinônimo(s):

Anti-CDMP2, Anti-GDF16, Anti-Growth differentiation factor 6

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About This Item

Código UNSPSC:
12352203
NACRES:
NA.41
conjugado:
unconjugated
application:
ELISA (i)
WB
clone:
polyclonal
reatividade de espécies:
mouse, human, rat
citations:
6
técnica(s):
indirect ELISA: suitable
western blot: suitable

fonte biológica

rabbit

Nível de qualidade

conjugado

unconjugated

forma do anticorpo

affinity isolated antibody

tipo de produto de anticorpo

primary antibodies

clone

polyclonal

Formulário

buffered aqueous solution

reatividade de espécies

mouse, human, rat

técnica(s)

indirect ELISA: suitable
western blot: suitable

nº de adesão UniProt

Condições de expedição

dry ice

temperatura de armazenamento

−20°C

modificação pós-traducional do alvo

unmodified

Informações sobre genes

human ... GDF6(392255)

Descrição geral

Growth differentiation factor 6 (GDF6) is a secreted signalling molecule, that belongs to the family of bone morphogenetic protein (BMP). Gdf6 is expressed in embryonic tissues that is concerned with patterning of skeletal and soft tissue. In human chromosome, the gene GDF6 is localized on 8q22.1.

Imunogênio

a 17 amino acid peptide near the carboxy-terminus of the human GDF6.

Aplicação

Anti-GDF6 antibody produced in rabbit has been used in western blotting.

Ações bioquímicas/fisiológicas

Growth differentiation factor 6 (GDF6) plays a crucial role in the joint formation during skeletal development. Gdf6 is involved in the maintenance of articular cartilage of knee. Mutation of GDF6 leads to loss-of-function and causes Klippel-Feil syndrome. Microduplication of GDF6 leads to an autosomal-dominant rheumatic condition, Leri′s pleonosteosis (LP). Mutations in GDF6 causes Multiple synostoses syndrome subtype SYNS4. In SYNS4, there is fusion of joints leading to progressive conductive deafness. GDF6 plays a key role in ocular development and the mutation of GDF6 leads to microphthalmia and anophthalmia. Mutations in GDF6 also leads to Leber congenital amaurosis-17.

Ligação

The action of this antibody can be blocked using blocking peptide SBP4691.

forma física

Solution in phosphate buffered saline containing 0.02% sodium azide

Exoneração de responsabilidade

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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Nº do produto
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Preços

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable


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Eye and neural defects associated with loss of GDF6
Hanel ML and Hensey C
BMC Developmental Biology, 6(1), 43-43 (2006)
A new subtype of multiple synostoses syndrome is caused by a mutation in GDF6 that decreases its sensitivity to noggin and enhances its potency as a BMP signal
Wang J, et al.
Journal of Bone and Mineral Research, 31(4), 882-889 (2016)
Growth differentiation factor 6 derived from mesenchymal stem/stromal cells reduces age-related functional deterioration in multiple tissues
Hisamatsu D, et al.
Aging (Albany. NY.), 8(6), 1259-1259 (2016)
GDF6, a novel locus for a spectrum of ocular developmental anomalies
Asai-Coakwell M, et al.
American Journal of Human Genetics, 80(2), 306-315 (2007)
Daisuke Hisamatsu et al.
Aging, 8(6), 1259-1275 (2016-06-18)
The senescence-associated secretory phenotype (SASP) has attracted attention as a mechanism that connects cellular senescence to tissue dysfunction, and specific SASP factors have been identified as systemic pro-aging factors. However, little is known about the age-dependent changes in the secretory

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