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Merck
CN

AV48390

Sigma-Aldrich

Anti-LZTFL1 antibody produced in rabbit

IgG fraction of antiserum

别名:

Anti-FLJ36386, Anti-Leucine zipper transcription factor-like 1

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UNSPSC代码:
12352203
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生物来源

rabbit

偶联物

unconjugated

抗体形式

IgG fraction of antiserum

抗体产品类型

primary antibodies

克隆

polyclonal

表单

buffered aqueous solution

分子量

34 kDa

种属反应性

pig, human, rat, bovine, mouse

浓度

0.5 mg - 1 mg/mL

技术

western blot: suitable

NCBI登记号

UniProt登记号

运输

wet ice

储存温度

−20°C

靶向翻译后修饰

unmodified

基因信息

human ... LZTFL1(54585)

一般描述

Leucine zipper transcription factor-like 1 (LZTFL1) is a cytoplasmic protein that interacts with Bardet-Biedl Syndrome (BBS) proteins and regulates their ciliary trafficking. Mutations in this leucine zipper gene have been linked to mesoxial polydactyly in BBS patients. It is also involved in the attenuation of cognitive impairment.
Rabbit Anti-LZTFL1 antibody recognizes human, mouse, rat, canine, zebrafish, and bovine LZTFL1.

免疫原

Synthetic peptide directed towards the C terminal region of human LZTFL1

应用

Rabbit Anti-LZTFL1 antibody is suitable for western blot applications at a concentration of 2.5 μg/ml.

外形

Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.

其他说明

Synthetic peptide located within the following region: VQEQLHMAEKELEKKFQQTAAYRNMKEILTKKNDQIKDLRKRLAQYEPED

免责声明

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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储存分类代码

12 - Non Combustible Liquids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

新产品
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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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E Schaefer et al.
Clinical genetics, 85(5), 476-481 (2013-05-23)
Ciliopathies are heterogeneous disorders sharing different clinical signs due to a defect at the level of the primary cilia/centrosome complex. Postaxial polydactyly is frequently reported in ciliopathies, especially in Bardet-Biedl syndrome (BBS). Clinical features and genetic results observed in a
Takuya Sakurai et al.
Biochemical and biophysical research communications, 416(1-2), 125-129 (2011-11-19)
It is well known that exercise prevents and reduces cognitive impairment. In the present study, we focused on exercise training as a tool to prevent cognitive impairment, and searched for novel molecules that may relate to the prevention of cognitive
Seongjin Seo et al.
PLoS genetics, 7(11), e1002358-e1002358 (2011-11-11)
Many signaling proteins including G protein-coupled receptors localize to primary cilia, regulating cellular processes including differentiation, proliferation, organogenesis, and tumorigenesis. Bardet-Biedl Syndrome (BBS) proteins are involved in maintaining ciliary function by mediating protein trafficking to the cilia. However, the mechanisms

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