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| 產(chǎn)地 | 進(jìn)口、國(guó)產(chǎn) |
| 品牌 | 上海莼試 |
| 保存條件 | Store at -20 °C |
| 貨號(hào) | CS11347 |
| 應(yīng)用范圍 | WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 |
| CAS編號(hào) | |
| 抗體名 | Anti-SPG7/Paraplegin |
| 克隆性 | |
| 靶點(diǎn) | 詳見(jiàn)說(shuō)明書(shū) |
| 適應(yīng)物種 | 詳見(jiàn)說(shuō)明書(shū) |
| 形態(tài) | 詳見(jiàn)說(shuō)明書(shū) |
| 宿主 | 詳見(jiàn)說(shuō)明書(shū) |
| 亞型 | IgG |
| 標(biāo)識(shí)物 | 詳見(jiàn)說(shuō)明書(shū) |
| 濃度 | 1mg/1ml% |
| 免疫原 | KLH conjugated synthetic peptide derived from human Paraplegin (201-285aa) |
全、新、優(yōu)、品、好四大特點(diǎn)：
痙攣性蛋白7/基質(zhì)細(xì)胞粘附調(diào)節(jié)蛋白抗體品牌 全：公司提供上萬(wàn)種產(chǎn)品，涵蓋了生物試劑，elisa試劑盒，標(biāo)準(zhǔn)品，培養(yǎng)基，原裝耗材，抗體、培養(yǎng)基、ATCC細(xì)胞等，基本上各種科研所需產(chǎn)品在我司都能找到。
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優(yōu)：產(chǎn)品質(zhì)量好，投訴比較少。
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痙攣性蛋白7/基質(zhì)細(xì)胞粘附調(diào)節(jié)蛋白抗體品牌 英文名稱(chēng) Anti-SPG7/Paraplegin
中文名稱(chēng) 痙攣性蛋白7/基質(zhì)細(xì)胞粘附調(diào)節(jié)蛋白抗體品牌
別 名 CAR; Cell adhesion regulator; Cell matrix adhesion regulator; CMAR; Paraplegin; PGN; Spastic paraplegia 7 (pure and complicated autosomal recessive); Spastic paraplegia 7 homolog (human); Spastic paraplegia 7, paraplegin (pure and complicated autosomal recessive); Spastic paraplegia protein 7; SPG5C; SPG7 gene; SPG7_HUMAN.
產(chǎn)品屬性：
濃 度 1mg/1ml
規(guī) 格 0.2ml/200μg
抗體來(lái)源 Rabbit
克隆類(lèi)型 polyclonal
交叉反應(yīng) Human, Mouse, Rat
產(chǎn)品類(lèi)型 一抗
研究領(lǐng)域 心 細(xì)胞生物 神經(jīng)生物學(xué) 細(xì)胞粘附分子
蛋白分子量 predicted molecular weight: 88kDa
性 狀 Lyophilized or Liquid
免 疫 原 KLH conjugated synthetic peptide derived from human Paraplegin (201-285aa)
亞 型 IgG
純化方法 affinity purified by Protein A
儲(chǔ) 存 液 Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4
痙攣性蛋白7/基質(zhì)細(xì)胞粘附調(diào)節(jié)蛋白抗體品牌 產(chǎn)品應(yīng)用 WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500
（石蠟切片需做抗原修復(fù)）
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
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.
Important Note This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
產(chǎn)品介紹 Paraplegin is a 795 amino acid metalloprotease that is a member of the AAA protein family. Localized to the mitochrondrial membrane and expressed throughout the body, Paraplegin is a multi-pass membrane protein that is thought to be involved in signal transduction and chaperone-like activities in the mitochrondria. Defects in the gene encoding Paraplegin are the cause of spastic paraplegia type 7 (SPG7), a form of autosomal recessive hereditary spastic paraplegia (AR-HSP). HSPs are degenerative spinal cord disorders that are characterized by muscle spasms, stiffness in the legs and, in some cases, incontinence. Recent studies suggest that SPG7 may be a mitochondrial-based disease, as mutations in the Paraplegin gene lead to ragged-red fibers, oxidase-negative fibers and intense succinate dehydrogenase-stained areas of the mitochrondria. These mitochondrial dysfunctions lead to axonal degeneration and impaired axonal transport, thus causing the neurodegeneration seen in HSPs.
Function : SPG7 is a metalloprotease protein that is a member of the AAA (ATPases associated with a variety of cellular activities) protein family. Members of this protein family share an ATPase domain and have roles in diverse cellular processes including membrane trafficking, intracellular motility, organelle biogenesis, protein folding, and proteolysis. Two transcript variants encoding distinct isoforms have been identified for this gene. Mutations associated with this gene cause autosomal recessive spastic paraplegia 7.
Subunit : Interacts with AFG3L2; the interaction is required forthe efficient assembly of mitochondrial complex I.
Subcellular Location : Mitochondrion membrane; Multi pass membrane protein.
Tissue Specificity : Ubiquitous.
DISEASE : Defects in SPG7 are the cause of spastic paraplegiaautosomal recessive type 7 (SPG7) [MIM:607259]. Spastic paraplegiais a degenerative spinal cord disorder characterized by a slow,gradual, progressive weakness and spasticity of the lower limbs.SPG7 is a complex form. Additional clinical features are cerebellarsyndrome, supranuclear palsy, and cognitive impairment,particularly disturbance of attention and executive functions.
Note=Defects in SPG7 may cause autosomal recessiveosteogenesis imperfecta (OI). Osteogenesis imperfecta defines agroup of connective tissue disorders characterized by bonefragility and low bone mass. Clinical features of SPG7-relatedosteogenesis imperfecta include recurrent fractures, mild bonedeformities, delayed tooth eruption, normal hearing and whitesclera.
Similarity : In the N-terminal section; belongs to the AAA ATPasefamily.
In the C-terminal section; belongs to the peptidaseM41 family.
Database links : UniProtKB/Swiss-Prot: Q9UQ90.2
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