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Rabbit Anti-TRIOBP/Gold Conjugated antibody (bs-17152R-Gold)
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說 明 書: 100ul(10nm  15nm  35nm
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-17152R-Gold
英文名稱 Rabbit Anti-TRIOBP/Gold Conjugated antibody
中文名稱 膠體金標記的TRIOBP蛋白抗體
別    名 DFNB28; KIAA1662; Protein TARA; TARA; TARA_HUMAN; Tara like protein; TRIO and F actin binding protein; Trio and filamentous actin binding protein; Trio associated repeat on actin.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul(10nm  15nm  35nm
研究領域 細胞生物  信號轉導  結合蛋白  細胞骨架  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit, Sheep, )
產(chǎn)品應用 IEM=1:20-200 ICA=1:20-200 ChIP=1:20-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 261kDa
性    狀 Lyophilized or Liquid
濃    度 0.4mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human TRIOBP
亞    型 IgG
純化方法 affinity purified by Protein A
儲 存 液 0.02M TBS(pH8.2) with 1% BSA, 0.03% Proclin300.
保存條件 Store at 2-8 oC for 3-6 months. Avoid repeated freeze/thaw cycles.
產(chǎn)品介紹 background:
This gene encodes a protein with an N-terminal pleckstrin homology domain and a C-terminal coiled-coil region. The protein interacts with trio, which is involved with neural tissue development and controlling actin cytoskeleton organization, cell motility and cell growth. The protein also associates with F-actin and stabilizes F-actin structures. Mutations in this gene have been associated with a form of autosomal recessive nonsyndromic deafness. Multiple alternatively spliced transcript variants that would encode different isoforms have been found for this gene, however some transcripts may be subject to nonsense-mediated decay (NMD). [provided by RefSeq, Nov 2008]

Function:
TRIOBP is a protein that interacts with trio, which is involved with neural tissue development and controlling actin cytoskeleton organization, cell motility and cell growth. This trio binding protein also associates with F actin and stabilizes F actin structures.

Subunit:
Binds to TRIO and F-actin. May also interact with myosin II. Interacts with HECTD3.

Subcellular Location:
Nucleus. Cytoplasm; cytoskeleton. Note: Localized to F-actin in a periodic pattern.

Tissue Specificity:
Widely expressed. Highly expressed in heart and placenta. Isoform 3 is expressed in fetal brain, retina and cochlea but is not detectable in the other tissues.

Post-translational modifications:
Ubiquitinated by HECTD3, leading to its degradation by the proteasome.
Isoform 1: Phosphorylation at Thr-457 by PLK1 ensures mitotic progression and is essential for accurate chromosome segregation.

DISEASE:
Deafness, autosomal recessive, 28 (DFNB28) [MIM:609823]: A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. Note=The disease is caused by mutations affecting the gene represented in this entry.

Similarity:
Contains 1 PH domain.

Database links:

Entrez Gene: 11078 Human

Entrez Gene: 511680 Cow

Entrez Gene: 110253 Mouse

Entrez Gene: 362956 Rat

Omim: 609761 Human

SwissProt: Q9H2D6 Human

SwissProt: Q99KW3 Mouse

Unigene: 533030 Human

Unigene: 123714 Mouse

Unigene: 119950 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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