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        Rabbit Anti-phospho-LIM Kinase 1 (Thr508)/BF488 Conjugated antibody (bs-18256R-BF488)
        訂購熱線:400-901-9800
        訂購郵箱:sales@bioss.com.cn
        訂購QQ:  400-901-9800
        技術支持:techsupport@bioss.com.cn
        說 明 書: 100ul  
        100ul/2980.00元
        大包裝/詢價
        產品編號 bs-18256R-BF488
        英文名稱 Rabbit Anti-phospho-LIM Kinase 1 (Thr508)/BF488 Conjugated antibody
        中文名稱 BF488標記的磷酸化單絲氨酸蛋白激酶1抗體
        別    名 LIM Kinase 1 (phospho T508); p-LIM Kinase 1 (phospho T508); LIMK1 (phospho T508);p-LIMK1 (phospho T508); EC 2.7.1.37; LIM domain containing protein kinase; LIM domain kinase 1; LIM motif containing protein kinase; LIMK 1; LIMK; LIMK-1; limk1; LIMK1_HUMAN.   
        規格價格 100ul/2980元 購買        大包裝/詢價
        說 明 書 100ul  
        產品類型 磷酸化抗體 
        研究領域 細胞生物  免疫學  發育生物學  神經生物學  信號轉導  激酶和磷酸酶  
        抗體來源 Rabbit
        克隆類型 Polyclonal
        交叉反應 Mouse, Rat,  (predicted: Human, Chicken, Pig, Cow, Horse, Sheep, )
        產品應用 ICC=1:50-200 IF=1:50-200 
        not yet tested in other applications.
        optimal dilutions/concentrations should be determined by the end user.
        分 子 量 73kDa
        性    狀 Lyophilized or Liquid
        濃    度 1mg/ml
        免 疫 原 KLH conjugated synthesised phosphopeptide derived from human LIM Kinase 1 around the phosphorylation site of Thr508
        亞    型 IgG
        純化方法 affinity purified by Protein A
        儲 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol
        保存條件 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.
        產品介紹 background:
        There are approximately 40 known eukaryotic LIM proteins, so named for the LIM domains they contain. LIM domains are highly conserved cysteine-rich structures containing 2 zinc fingers. Although zinc fingers usually function by binding to DNA or RNA, the LIM motif probably mediates protein-protein interactions. LIM kinase-1 and LIM kinase-2 belong to a small subfamily with a unique combination of 2 N-terminal LIM motifs and a C-terminal protein kinase domain. LIMK1 is a serine/threonine kinase that regulates actin polymerization via phosphorylation and inactivation of the actin binding factor cofilin. This protein is ubiquitously expressed during development and plays a role in many cellular processes associated with cytoskeletal structure. This protein also stimulates axon growth and may play a role in brain development. LIMK1 hemizygosity is implicated in the impaired visuospatial constructive cognition of Williams syndrome. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Feb 2011]

        Function:
        Protein kinase which regulates actin filament dynamics. Phosphorylates and inactivates the actin binding/depolymerizing factor cofilin, thereby stabilizing the actin cytoskeleton. Stimulates axonal outgrowth and may be involved in brain development. Isoform 3 has a dominant negative effect on actin cytoskeletal changes.

        Subcellular Location:
        Cytoplasm. Cell projection > growth cone.

        Tissue Specificity:
        Highest expression in both adult and fetal nervous system. Detected ubiquitously throughout the different regions of adult brain, with highest levels in the cerebral cortex. Expressed to a lesser extent in heart and skeletal muscle.

        Post-translational modifications:
        Autophosphorylated.
        Phosphorylated on serine and/or threonine residues by ROCK1.
        May be dephosphorylated and inactivated by SSH1.
        Ubiquitinated. 'Lys-48'-linked polyubiquitination by RNF6 leads to proteasomal degradation through the 26S proteasome, modulating LIMK1 levels in the growth cone and its effect on axonal outgrowth. Also polyubiquitinated by RLIM.

        DISEASE:
        Note=LIMK1 is located in the Williams-Beuren syndrome (WBS) critical region. WBS results from a hemizygous deletion of several genes on chromosome 7q11.23, thought to arise as a consequence of unequal crossing over between highly homologous low-copy repeat sequences flanking the deleted region.

        Similarity:
        Belongs to the protein kinase superfamily.
        TKL Ser/Thr protein kinase family.
        Contains 2 LIM zinc-binding domains.
        Contains 1 PDZ (DHR) domain.
        Contains 1 protein kinase domain.

        Database links:

        Entrez Gene: 3984 Human

        Entrez Gene: 16885 Mouse

        Entrez Gene: 65172 Rat

        Omim: 601329 Human

        SwissProt: P53667 Human

        SwissProt: P53668 Mouse

        SwissProt: P53669 Rat

        Unigene: 647035 Human

        Unigene: 15409 Mouse

        Unigene: 11250 Rat



        Important Note:
        This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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