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phospho-Brk (Tyr447)抗体

phospho-Brk (Tyr447)抗体
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简单介绍
phospho-Brk (Tyr447)抗体这个编码蛋白是一种细胞质的非受体蛋白激酶的功能可能在上皮组织细胞内��信号转导。该基因在乳腺上皮细胞中的过表达导致细胞对表皮生长因子的敏感性,并导致部分转化表型。该基因在某些乳腺肿瘤组织中的表达水平较低,而在正常乳腺组织中却未检测到。phospho-Brk (Tyr447)抗体它在细胞核中的存在似乎与抑制肿瘤进展有关。其编码的蛋白质已被证明发生磷酸化。
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phospho-Brk (Tyr447)抗体ICC, IHC严格验证,品质保证.适用于多种种属反应性,被多篇文献引用并有用户反馈信息.确保特异性!产品具有以下特点:

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产品编号xy-12890R

英文名称phospho-Brk (Tyr447)

中文名称磷酸化酪氨酸蛋白激酶6/乳腺肿瘤激酶抗体

别    名Brk (phospho Y447); p-Brk (phospho Y447); Breast tumor kinase; Breast tumour kinase; Protein tyrosine kinase 6; PTK6; Tyrosine protein kinase BRK; PTK6_HUMAN.  

JournalPMIDIFApplicationMarine Drugs (2014)247368073.9780IHC-P

说 明 书100ul  

产品类型磷酸化抗体

研究领域肿瘤  细胞生物  信号转导  激酶和磷酸酶  

抗体来源Rabbit

克隆类型Polyclonal

phospho-Brk (Tyr447)抗体交叉反应 Human,

产品应用WB=1:500-2000 ELISA=1:500-1000 IHC-P=1:400-800 IHC-F=1:400-800 Flow-Cyt=3μg/Test ICC=1:100-500 IF=1:100-500 (石蜡切片需做抗原修复)

not yet tested in other applications.

optimal dilutions/concentrations should be determined by the end user.

分 子 量52kDa

性    状Lyophilized or Liquid

浓    度1mg/1ml

免 疫 原KLH conjugated synthesised phosphopeptide derived from human Brk around the phosphorylation site of Tyr447 [TS(p-Y)EN]

亚    型IgG

纯化方法affinity purified by Protein A

储 存 液0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.

保存条件Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.

PubMedPubMed

产品介绍background:

This protein encoded is a cytoplasmic nonreceptor protein kinase which may function as an intracellular signal transducer in epithelial tissues. Overexpression of this gene in mammary epithelial cells leads to sensitization of the cells to epidermal growth factor and results in a partially transformed phenotype. Expression of this gene has been detected at low levels in some breast tumors but not in normal breast tissue. Its presence in the nucleus appears to be linked to suppression of tumor progression. The encoded protein has been shown to undergo autophosphorylation.


Function:

Non-receptor tyrosine-protein kinase implicated in the regulation of a variety of signaling pathways that control the differentiation and maintenance of normal epithelia, as well as tumor growth. Function seems to be context dependent and differ depending on cell type, as well as its intracellular localization. A number of potential nuclear and cytoplasmic substrates have been identified. These include the RNA-binding proteins: KHDRBS1/SAM68, KHDRBS2/SLM1, KHDRBS3/SLM2 and SFPQ/PSF; transcription factors: STAT3 and STAT5A/B and a variety of signaling molecules: ARHGAP35/p190RhoGAP, PXN/paxillin, BTK/ATK, STAP2/BKS. Associates also with a variety of proteins that are likely upstream of PTK6 in various signaling pathways, or for which PTK6 may play an adapter-like role. These proteins include ADAM15, EGFR, ERBB2, ERBB3 and IRS4. In normal or non-tumorigenic tissues, PTK6 promotes cellular differentiation and apoptosis. In tumors PTK6 contributes to cancer progression by sensitizing cells to mitogenic signals and enhancing proliferation, anchorage-independent survival and migration/invasion. Association with EGFR, ERBB2, ERBB3 may contribute to mammary tumor development and growth through enhancement of EGF-induced signaling via BTK/AKT and PI3 kinase. Contributes to migration and proliferation by contributing to EGF-mediated phosphorylation of ARHGAP35/p190RhoGAP, which promotes association with RASA1/p120RasGAP, inactivating RhoA while activating RAS. EGF stimulation resulted in phosphorylation of PNX/Paxillin by PTK6 and activation of RAC1 via CRK/CrKII, thereby promoting migration and invasion. PTK6 activates STAT3 and STAT5B to promote proliferation. Nuclear PTK6 may be important for regulating growth in normal epithelia, while cytoplasmic PTK6 might activate oncogenic signaling pathways.


Subunit:

Interacts with GAP-A.p65. Interacts (via SH3 and SH2 domains) with KHDRBS1. Interacts (via SH3 and SH2 domains) with phosphorylated IRS4. Interacts with ADAM15. Interacts (via SH3 domain) with SFPQ. Interacts with EGFR and ERBB2. Interacts with STAP2. Interacts with PNX. Interacts with SFPQ. Interacts with PTK/ATK. Interacts with CTNNB1.


Subcellular Location:

Epithelia-specific. Very high level in colon and high levels in small intestine and prostate, and low levels in some fetal tissues. Not expressed in breast or ovarian tissue but expressed in high pourcentage of breast and ovarian cancers. Also overexpressed in some metastatic melanomas, lymphomas, colon cancers, squamous cell carcinomas and prostate cancers. Also found in melanocytes. Not expressed in heart, brain, placenta, lung, liver, skeletal muscle, kidney and pancreas. Isoform 2 is present in prostate epithelial cell lines derived from normal prostate and prostate adenocarcinomas, as well as in a variety of cell lines.


Tissue Specificity:

Epithelia-specific. Very high level in colon and high levels in small intestine and prostate, and low levels in some fetal tissues. Not expressed in breast or ovarian tissue but expressed in high pourcentage of breast and ovarian cancers. Also overexpressed in some metastatic melanomas, lymphomas, colon cancers, squamous cell carcinomas and prostate cancers. Also found in melanocytes. Not expressed in heart, brain, placenta, lung, liver, skeletal muscle, kidney and pancreas. Isoform 2 is present in prostate epithelial cell lines derived from normal prostate and prostate adenocarcinomas, as well as in a variety of cell lines.


Post-translational modifications:

Autophosphorylated. Autophosphorylation of Tyr-342 leads to an increase of kinase activity. Tyr-447 binds to the SH2 domain when phosphorylated and negatively regulates kinase activity.


Similarity:

Belongs to the protein kinase superfamily. Tyr protein kinase family. BRK/PTK6/SIK subfamily.

Contains 1 protein kinase domain.

Contains 1 SH2 domain.

Contains 1 SH3 domain.


SWISS:

Q13882


Gene ID:

5753

抗体选择指南

phospho-Brk (Tyr447)抗体检测任何目的靶蛋白都有不止一种抗体可供选择,为缩小抗体的选择范围选中合适的抗体,需要考虑如下几种因素:

1 分析或应用的类型

2)样本蛋白的结构性质

3)样本的种属

4)抗体宿主的种类

5)抗体的标记和检测

1 分析试验的应用类型一般抗体说明书都列出该抗体经试验验证过适用于何种分析类型,如:

可以应用于WB IHC ICC ELASA 分析等,如果抗体说明书没有提及的应用类型,并不意味着该抗体不适用于此种分析应用类型,而仅是说明尚未经过此种分析试验验证,如果抗体不适用某些分析试验,则会在抗体说明书上标注出来不适于某分析试验。

2 样本蛋白的结构性质了解样本蛋白的结构性质有助于选择*合适的抗体,至少需要考虑两方面因素

(1)..待测样本蛋白的结构域:phospho-Brk (Tyr447)抗体是由各种不同**原**宿主而制备得来,其中的**原包括:全长蛋白、蛋白片断、多肽、全有机体(如:**)或细胞,抗体说明书一般都有**原的描述,如果打算检测的是蛋白片断或一种特殊的同型物或蛋白全长的某一区域,则必须选择用含此片段域的**原制备出的抗体。如果打算用FACS 流式检测活细胞的表面蛋白,则需要选择含该表面蛋白的胞外域来**制备的抗体。

(2)样本的提取或处理过程:某些抗体要求样本经过某些特殊处理,例如:许多抗体只识别还原和变性的、表位已暴露不受二级四级结构阻碍的蛋白样本,另一方面,某些抗体仅识别天然折叠状态的蛋白。

当选择**组化的抗体时,应注意某些抗体只识别未固定的冷冻的组织,而另一些抗体则适用于无需抗原修复解交联步聚的甲醛固定石蜡包埋的组织,这些都会在抗体说明书上应用部分标示出来 3 样本的物种 应选择物种相同或有交叉反应的抗体,抗体可能与不同物种的同种靶蛋白有交叉反应,因其氨基酸序列同源性较高。

如果样本的种类未列入抗体说明书上的交叉反应种属表中,并不意味着该抗体不适用于检测该物种的蛋白,而只是表示该物种尚未用此抗体检测验证过,应通过序列比对的方法来预测交叉反应,phospho-Brk (Tyr447)抗体可应用Expasy NCBI BLAST 来进行不同物种蛋白同源性比对。

4 一抗宿主物种的选择一般说来,在使用偶联二抗结合无偶联物的一抗时,一抗宿主动物的物种选择较为重要,对于**组化而言,尽可能选择与样本不同种系物种的一抗,从而避免二抗与样本内源性**球蛋白产生交叉反应,

例如:检测小鼠样本蛋白,则不应选择小鼠或大鼠源的一抗,*好选兔源的一抗,则二抗则可选择偶联了检测分子(酶、荧光素、生物素等)的抗兔IgG。如果选择有偶联物的一抗则不适用上述情况,除**组化外的其它对不含内源性**球蛋白样本的检测方法,则抗体宿主物种的影响不大,如对不含IgG 的细胞裂解物样本的western blotting检测。

尽管如此,phospho-Brk (Tyr447)抗体含有血清的组织裂解物和组织培养上清中含有**球蛋白,还原变性样本中含IgG,在western blot 检测中则结合出现IgG 分子50 and 25 kDa 的重链和轻链条带。

5 二抗的选择 二抗应选用与使用的一抗相同的物种来源,例如:如果你的一抗是小鼠的单克隆抗体,二抗则选抗小鼠的二抗anti-mouse secondary。建议检查二抗说明书确保该抗体适用于你的检测应用, 二抗一般连接荧光素FITC 或发光团。

6 双重染色抗体的选择用未偶联一抗进行细胞培养物或组织切片的双重**染色要求一抗来源于不同物种并且二抗分别识别其中之一,二抗说明书应描述其与其它物种来源的**球蛋有否有交叉吸附。

合格 合格 合格 JNK1 + JNK3 氨基末端激酶1/3抗体
合格 合格 CD18 整合素β2/Integrin β2抗体
合格 PRL 泌乳素抗体
合格 RAR  Beta 维甲酸受体β抗体
合格 CD44 CD44抗体
合格 CD45 白细胞共同抗原CD45抗体 
合格 合格 SOX2 胚胎干细胞关键蛋白抗体
合格 ALOX5/5 lipoxygenase 5-脂氧合酶抗体
合格 合格 CD10 CD10抗体
合格 CD24 CD24抗体
合格 IL-18 白细胞介素-18/干扰素γ诱导因子抗体
合格 合格 PPAR gamma 过氧化酶活化增生受体γ抗体
合格 合格 Matriptase 蛋白裂解酶(一种新的癌基因)抗体
合格 合格 TFF3 三叶肽因子3抗体
合格 Interferon alpha 2b 干扰素α2b抗体
合格 ANGPTL2 血管生成素样蛋白2抗体
合格 CAMK2A + CAMK2B + CAMK2D 钙/钙调素依赖蛋白激酶2b/2γ抗体
合格 CDK1 周期素依赖性激酶1抗体

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