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FITC標記的(dí)AFG3樣蛋(dàn)白(bái)2/脊髓小腦(nǎo)共(gòng)濟(jì)失(shī)調蛋(dàn)白28抗(kàng)體(tǐ)
文(wén)字：[大][中(zhōng)][小(xiǎo)]
2017-5-2 瀏覽次(cì)數：1614
英文名稱(chēng)Anti-AFG3L2/FITC
中文名(míng)稱(chēng):FITC標記(jì)的(dí)AFG3樣(yàng)蛋(dàn)白(bái)2/脊髓(suǐ)小腦(nǎo)共(gòng)濟失調(tiáo)蛋白28抗(kàng)體
別 名(míng)SCA28; AFG3 (ATPase family gene 3, yeast) like 2; AFG3 ATPase family gene 3 like 2 (yeast); AFG3 ATPase family gene 3 like 2; AFG3 like protein 2; ATPase family gene 3 like 2; ATPase family gene 3 yeast; FLJ25993; Paraplegin like protein; SCA28; Spinocerebellar ataxia 28; AFG32_HUMAN .
規(guī)格:100ul
說 明(míng) 書100ul
研究領域腫瘤 細胞生物 神(shén)經(jīng)生(shēng)物(wù)學 信(xìn)號(hào)轉(zhuǎn)導 泛素(sù)
抗體(tǐ)來源(yuán)Rabbit
克(kè)隆類(lèi)型(xíng)Polyclonal
交(jiāo)叉反(fǎn)應 Human, Mouse, Rat, Chicken, Dog, Pig, Cow, Horse, Sheep,
產品(pǐn)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(liáng)89kDa
細胞定(dìng)位細胞(bāo)膜
性 狀(zhuàng)Lyophilized or Liquid
濃(nóng) 度(dù)1mg/ml
免(miǎn) 疫 原KLH conjugated synthetic peptide derived from human AFG3L2 (531-600aa)
亞 型IgG
純(chún)化方法affinity purified by Protein A
儲(chǔ) 存(cún) 液(yè)0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保(bǎo)存(cún)條(tiáo)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(shào)background:
AFG3L2 is a multi-pass membrane metalloprotease that contains one AAA (ATPase associated with diverse cellular activities) domain, a zinc-dependent binding motif, an RNA-binding region and an ATP/GTP binding site. Localizing to the mitochondrial membrane, AFG3L2 is ubiquitously expressed with highest expression levels in skeletal muscle and heart. AFG3L2 shares 69% similarity with the yeast Afg3 protein and 49% similarity with Paraplegin, a protein of mitochondria that is thought to be involved in signal transduction and chaperone-like activities. In mitochondria, AFG3L2 forms a complex with Paraplegin that is believed to regulate essential protein quality control. Mutations in the gene encoding either one of these proteins can result in hereditary spastic paraplegia, a degenerative spinal cord disorder that is characterized by muscle spasms, stiffness in the legs and, in some cases, incontinence
Function:
AFG3L2 is a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. AFG3L2 is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders and is a putative ATP dependent protease
Subunit:
Homooligomer. Interacts with SPG7; the interaction is required for the efficient assembly of mitochondrial complex I.
Subcellular Location:
Mitochondrial membrane; multipass membrane protein
Tissue Specificity:
Ubiquitous. Highly expressed in the cerebellar Purkinje cells.
中文名(míng)稱(chēng):FITC標記(jì)的(dí)AFG3樣(yàng)蛋(dàn)白(bái)2/脊髓(suǐ)小腦(nǎo)共(gòng)濟失調(tiáo)蛋白28抗(kàng)體
別 名(míng)SCA28; AFG3 (ATPase family gene 3, yeast) like 2; AFG3 ATPase family gene 3 like 2 (yeast); AFG3 ATPase family gene 3 like 2; AFG3 like protein 2; ATPase family gene 3 like 2; ATPase family gene 3 yeast; FLJ25993; Paraplegin like protein; SCA28; Spinocerebellar ataxia 28; AFG32_HUMAN .
詳細(xì)介紹(shào)：
規(guī)格:100ul
說 明(míng) 書100ul
研究領域腫瘤 細胞生物 神(shén)經(jīng)生(shēng)物(wù)學 信(xìn)號(hào)轉(zhuǎn)導 泛素(sù)
抗體(tǐ)來源(yuán)Rabbit
克(kè)隆類(lèi)型(xíng)Polyclonal
交(jiāo)叉反(fǎn)應 Human, Mouse, Rat, Chicken, Dog, Pig, Cow, Horse, Sheep,
產品(pǐn)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(liáng)89kDa
細胞定(dìng)位細胞(bāo)膜
性 狀(zhuàng)Lyophilized or Liquid
濃(nóng) 度(dù)1mg/ml
免(miǎn) 疫 原KLH conjugated synthetic peptide derived from human AFG3L2 (531-600aa)
亞 型IgG
純(chún)化方法affinity purified by Protein A
儲(chǔ) 存(cún) 液(yè)0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保(bǎo)存(cún)條(tiáo)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.
相關資料(liào)：
產品介紹(shào)background:
AFG3L2 is a multi-pass membrane metalloprotease that contains one AAA (ATPase associated with diverse cellular activities) domain, a zinc-dependent binding motif, an RNA-binding region and an ATP/GTP binding site. Localizing to the mitochondrial membrane, AFG3L2 is ubiquitously expressed with highest expression levels in skeletal muscle and heart. AFG3L2 shares 69% similarity with the yeast Afg3 protein and 49% similarity with Paraplegin, a protein of mitochondria that is thought to be involved in signal transduction and chaperone-like activities. In mitochondria, AFG3L2 forms a complex with Paraplegin that is believed to regulate essential protein quality control. Mutations in the gene encoding either one of these proteins can result in hereditary spastic paraplegia, a degenerative spinal cord disorder that is characterized by muscle spasms, stiffness in the legs and, in some cases, incontinence
Function:
AFG3L2 is a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. AFG3L2 is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders and is a putative ATP dependent protease
Subunit:
Homooligomer. Interacts with SPG7; the interaction is required for the efficient assembly of mitochondrial complex I.
Subcellular Location:
Mitochondrial membrane; multipass membrane protein
Tissue Specificity:
Ubiquitous. Highly expressed in the cerebellar Purkinje cells.
