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Merck

SAB1401533

Sigma-Aldrich

Monoclonal Anti-SIX2 antibody produced in mouse

clone 1G11, purified immunoglobulin, buffered aqueous solution

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100 μG
¥81,000

¥81,000


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100 μG
¥81,000

About This Item

UNSPSCコード:
12352203
NACRES:
NA.41

¥81,000


Check Cart for Availability

由来生物

mouse

品質水準

結合体

unconjugated

抗体製品の状態

purified immunoglobulin

抗体製品タイプ

primary antibodies

クローン

1G11, monoclonal

フォーム

buffered aqueous solution

交差性

human

テクニック

capture ELISA: suitable
western blot: 1-5 μg/mL

アイソタイプ

IgG1κ

NCBIアクセッション番号

UniProtアクセッション番号

輸送温度

dry ice

保管温度

−20°C

ターゲットの翻訳後修飾

unmodified

遺伝子情報

human ... SIX2(10736)

詳細

This gene is a member of the vertebrate gene family which encode proteins homologous to the Drosophila ′sine oculis′ homeobox protein. The encoded protein is a transcription factor which, like other members of this gene family, may be involved in limb or eye development. (provided by RefSeq)

免疫原

SIX2 (AAH24033, 1 a.a. ~ 291 a.a) full-length recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.

Sequence
MSMLPTFGFTQEQVACVCEVLQQGGNIERLGRFLWSLPACEHLHKNESVLKAKAVVAFHRGNFRELYKILESHQFSPHNHAKLQQLWLKAHYIEAEKLRGRPLGAVGKYRVRRKFPLPRSIWDGEETSYCFKEKSRSVLREWYAHNPYPSPREKRELTEATGLTTTQVSNWFKNRRQRDRAAEAKERENNENSNSNSHNPLNGSGKSVLGSSEDEKTPSGTPDHSSSSPALLLSPPPPGLPSLHSLGHPPGPSAVPVPVPGGGGADPLQHHHGLQDSILNPMSANLVDLGS

生物化学的/生理学的作用

SIX2 (SIX homeobox 2) is responsible for the regulation of cartilage growth and differentiation in endochondral skeleton. SIX2 also participates in the craniofacial skeletal muscle formation. It might prevent the abnormal drooping eyelids, by weakening the ability of levator muscle to contract. SIX2 haploinsufficiency is linked with congenital ossicle malformation. Mutation in SIX2 is found to be associated with the development of urinary tract, kidney, anterior cranial base, limb tendon and the formation of pyloric sphincter. Deletion in the gene might cause autosomal dominant frontonasal dysplasia syndrome. Mutation in the gene leads to renal hypodysplasia and also chemotherapy-resistant blastemas.

物理的形状

無色透明のPBS溶液、pH 7.4

免責事項

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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保管分類コード

10 - Combustible liquids

引火点(°F)

Not applicable

引火点(℃)

Not applicable


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文書ライブラリにアクセスする

SIX2 haploinsufficiency causes conductive hearing loss with ptosis in humans.
Guan J
Journal of Human Genetics, 61(11), 917-922 (2016)
A new frontonasal dysplasia syndrome associated with deletion of the SIX2 gene.
Hufnagel RB
American Journal of Medical Genetics, 170A(2), 487-491 (2016)
Differential regulation of mouse and human nephron progenitors by the Six family of transcriptional regulators.
O'Brien LL
Development, 143(4), 595-608 (2016)
Nils O Lindström et al.
Journal of the American Society of Nephrology : JASN, 29(3), 825-840 (2018-02-17)
The nephron is the functional unit of the kidney, but the mechanism of nephron formation during human development is unclear. We conducted a detailed analysis of nephron development in humans and mice by immunolabeling, and we compared human and mouse

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