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Merck

SAB1402151

Sigma-Aldrich

Monoclonal Anti-COL1A1 antibody produced in mouse

clone 3G3, purified immunoglobulin, buffered aqueous solution

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About This Item

Kod UNSPSC:
12352203
NACRES:
NA.41

pochodzenie biologiczne

mouse

białko sprzężone

unconjugated

forma przeciwciała

purified immunoglobulin

rodzaj przeciwciała

primary antibodies

klon

3G3, monoclonal

Postać

buffered aqueous solution

masa cząsteczkowa

antigen ~35.79 kDa

reaktywność gatunkowa

human, mouse

metody

immunohistochemistry (formalin-fixed, paraffin-embedded sections): suitable
indirect ELISA: suitable
western blot: 1-5 μg/mL

izotyp

IgG3κ

numer dostępu NCBI

numer dostępu UniProt

Warunki transportu

dry ice

temp. przechowywania

−20°C

docelowa modyfikacja potranslacyjna

unmodified

informacje o genach

human ... COL1A1(1277)

Opis ogólny

The COL1A1 (collagen type I α 1 chain) gene codes for the pro-α1 chains of type I collagen. The triple helix of the type I collagen is composed of two α chains and this protein is localized to connective tissues and predominantly expressed in bone, cornea, dermis and tendon. COL1A1 is mapped to human chromosome 17q21.33. 90% of the bone matrix comprises of collagen type I.

Immunogen

COL1A1 (NP_000079.1, 1021 a.a. ~ 1108 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.

Sequence
EGSPGRDGSPGAKGDRGETGPAGPPGAPGAPGAPGPVGPAGKSGDRGETGPAGPAGPVGPVGARGPAGPQGPRGDKGETGEQGDRGIK

Działania biochem./fizjol.

Proteins belonging to the collagen family, supports and nourishes body tissues such as tendons, cartilage, skin, and sclera of the eye. Mutation in COL1A1 (collagen type I α 1 chain) gene is associated with a number of connective tissue disorders such as Ehlers-Danlos syndrome type VIIA, Ehlers-Danlos syndrome Classical type, osteogenesis imperfecta types I-IV, idiopathic osteoporosis and Caffey Disease. The COL1A1 is associated with a particular type of skin tumor called dermatofibrosarcoma protuberans which is due to over expression of growth factors. Two transcripts, resulting from the use of alternate polyadenylation signals, have been identified for this gene.

Postać fizyczna

Solution in phosphate buffered saline, pH 7.4

Oświadczenie o zrzeczeniu się odpowiedzialności

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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Kod klasy składowania

10 - Combustible liquids

Klasa zagrożenia wodnego (WGK)

WGK 1

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable


Certyfikaty analizy (CoA)

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Odwiedź Bibliotekę dokumentów

Nicolas R Chevalier et al.
Communications biology, 4(1), 770-770 (2021-06-25)
While the colonization of the embryonic gut by neural crest cells has been the subject of intense scrutiny over the past decades, we are only starting to grasp the morphogenetic transformations of the enteric nervous system happening in the fetal
Clinical utility gene card for: Ehlers?Danlos syndrome types I?VII and variants-update 2012.
Mayer K, et al.
European Journal of Human Genetics, 21(1) (2013)
Aspek Klinik, Genetik dan Molekuler Osteogensis Imperfekta.
Mariska M and Auerkari E I
Journal of Dentistry, 14(2), 95-110 (2015)
Epidemiology, genetics and treatments for myopia.
Yu L, et al.
International journal of ophthalmology, 4(6), 658-658 (2011)
Masamichi Hayashi et al.
BMC cancer, 14, 108-108 (2014-02-21)
Hepatocellular carcinoma (HCC) is one of the major causes of cancer-related death especially among Asian and African populations. It is urgent that we identify carcinogenesis-related genes to establish an innovative treatment strategy for this disease. Triple-combination array analysis was performed

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