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Rabbit Anti-Reelin/Cy5 Conjugated antibody (bs-1560R-Cy5)
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說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-1560R-Cy5
英文名稱1 Rabbit Anti-Reelin/Cy5 Conjugated antibody
中文名稱 Cy5標(biāo)記的絡(luò)絲蛋白抗體
別    名 Reelin; Reeler; RELN; RL; LIS2; PRO1598; RELN_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(xì)胞生物  免疫學(xué)  神經(jīng)生物學(xué)  細(xì)胞凋亡  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) Mouse,  (predicted: Human, Rat, Chicken, Dog, Pig, Horse, Guinea Pig, )
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 400-450;300;180-kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human RELN
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:
Reelin (or Reln) is a large glycoprotein that is secreted by Cajal-Retzius cells in the forebrain and by granule neurons in the cerebellum. Reelin was shown to be mutated in “reeler” mice, a mutation that is associated with widespread disruption of laminated regions of the brain, leading to impaired motor coordination, tremors and ataxia. Reelin protein expression is complex and changes throughout development. Reelin appears to function upstream of Dab1 in a signaling pathway that controls cell positioning in the developing brain and is also thought to be a direct effector of the neurotrophin BDNF.

Function:
This gene encodes a large secreted extracellular matrix protein thought to control cell-cell interactions critical for cell positioning and neuronal migration during brain development. This protein may be involved in schizophrenia, autism, bipolar disorder, major depression and in migration defects associated with temporal lobe epilepsy. Mutations of this gene are associated with autosomal recessive lissencephaly with cerebellar hypoplasia. Two transcript variants encoding distinct isoforms have been identified for this gene. Other transcript variants have been described but their full length nature has not been determined.

Subcellular Location:
Secreted

Tissue Specificity:
High level detected in plasma but also in extravascular fluids such as follicular and cerebrospinal fluids (at protein level).

Post-translational modifications:
N-glycosylated; more than 90% of the glycans are sialylated.

Similarity:
Belongs to the ALB/AFP/VDB family.
Contains 3 albumin domains.

Database links:

Entrez Gene: 5649 Human

Entrez Gene: 19699 Mouse

Entrez Gene: 24718 Rat

Omim: 600514 Human

SwissProt: P78509 Human

SwissProt: Q60841 Mouse

SwissProt: P58751 Rat

Unigene: 655654 Human

Unigene: 425236 Mouse

Unigene: 98353 Rat



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

Reelin蛋白作用目前還在進(jìn)一步研究中,但有學(xué)者認(rèn)為它與β-Amyloid 的神經(jīng)纏結(jié)有相對應(yīng)的作用。
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