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Rabbit Anti-CYFIP2/BF647 Conjugated antibody (bs-7606R-BF647)
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說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-7606R-BF647
英文名稱1 Rabbit Anti-CYFIP2/BF647 Conjugated antibody
中文名稱 BF647標記的細胞質(zhì)脆性X智力低下蛋白結(jié)合蛋白2抗體
別    名 CYFP2; cytoplasmic FMR1 interacting protein 2; KIAA1168; p53 inducible protein; p53-inducible protein 121; PIR121; CYFP2_HUMAN.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領(lǐng)域 細胞生物  神經(jīng)生物學(xué)  信號轉(zhuǎn)導(dǎo)  細胞凋亡  轉(zhuǎn)錄調(diào)節(jié)因子  t-淋巴細胞  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human, Mouse, Rat, Chicken, Dog, Pig, Horse, Rabbit, Sheep, )
產(chǎn)品應(yīng)用 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 148kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human CYFIP2
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(chǎn)品介紹 background:
CYFIP2 is involved in T cell adhesion and p53 dependent induction of apoptosis. It does not bind RNA but is up regulated significantly in CD4+ T lymphocytes from patients with multiple sclerosis. There are 2 isoforms produced by alternative splicing.

Function:
Involved in T-cell adhesion and p53/TP53-dependent induction of apoptosis. Does not bind RNA

Subunit:
Interacts with FMR1, FXR1 AND FXR2. Component of the WAVE1 complex composed of ABI2, CYFIP2, BRK1, NCKAP1 and WASF1/WAVE1. CYFIP2 binds to activated RAC1 which causes the complex to dissociate, releasing activated WASF1. The complex can also be activated by NCK1.

Subcellular Location:
Cytoplasm. Cytoplasm, perinuclear region. Cell junction , synapse, synaptosome. Note: Highly expressed in the perinuclear region. Enriched in synaptosomes. Treatment with leptomycin-B triggers translocation to the nucleus.

Tissue Specificity:
Expressed in T-cells. Increased expression is observed in CD4+ T-lymphocytes from patients with multiple sclerosis (at protein level).

Similarity:
Belongs to the CYFIP family.

Database links:
UniProtKB/Swiss-Prot: Q96F07.2

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

脆性X綜合癥,又稱馬丁-貝爾綜合癥,是一種遺傳疾病。該綜合癥可以導(dǎo)致一系列的特征性癥狀,包括生理、智力、情緒、以及行為上的異常。癥狀的輕重各有不同。該疾病伴隨著X染色體上一個簡單的三核苷酸基因序列(CGG)的擴增。這種擴增導(dǎo)致了一種稱為FMR-1的蛋白質(zhì)無法在病人體內(nèi)表達,而該蛋白質(zhì)是神經(jīng)的正常發(fā)育必不可少的。
根據(jù)CGG重復(fù)序列的長度,目前普遍認可將脆性X綜合癥分為四種類型:正常人(含有19-31個CGG重復(fù)序列),前突變者(含有55-200個CGG重復(fù)序列),全突變者(含有200個以上的CGG重復(fù)序列),過渡型,又稱“灰色區(qū)域型”(含有40-60個重復(fù))。脆性X綜合征這是一種導(dǎo)致智力低下的遺傳疾病,是導(dǎo)致人群中智力低下的第二大病因——僅次于21三體綜合癥。
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