Fukutin 抗体 (AA 222-456)
Quick Overview for Fukutin 抗体 (AA 222-456) (ABIN1886220)
抗原
See all Fukutin (FKTN) 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 222-456
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纯化方法
- Purified by antigen-affinity chromatography.
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免疫原
- Recombinant protein fragment contain a sequence corresponding to a region within amino acids 222 and 456 of Human FKTN
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anti-Fukutin (FKTN) (AA 272-456) antibody
FKTN 适用: 人 WB, IHC, IHC (p), IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Fukutin (FKTN) (AA 29-138) antibodyFKTN 适用: 人 WB, ELISA 宿主: 小鼠 Polyclonal unconjugated
anti-Fukutin (FKTN) (AA 111-160) antibodyFKTN 适用: 人, 大鼠, 犬, 马, 兔, Pig, Bat, 猴 WB, IHC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Fukutin (FKTN) antibodyFKTN 适用: 人 WB, IHC 宿主: 兔 Monoclonal unconjugated
anti-Fukutin (FKTN) antibodyFKTN 适用: 人 WB, IHC (p), IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Fukutin (FKTN) (N-Term) antibodyFKTN 适用: 人, 大鼠, 犬 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Fukutin (FKTN) (AA 87-276) antibodyFKTN 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Fukutin (FKTN) antibodyFKTN 适用: 人, 小鼠 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Fukutin (FKTN) (AA 177-206) antibodyFKTN 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal RB31283 unconjugated
anti-Fukutin (FKTN) (N-Term) antibodyFKTN 适用: 人, 小鼠, 大鼠, 犬, 马, 兔, 豚鼠, Cow, Pig WB, IHC 宿主: 兔 Polyclonal unconjugated
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应用备注
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Suggested dilutions:
Western blotting: 1.500-1.3000
Immunofluorescence: 1.100-1.200 -
限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- 0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.
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储存液
- Thimerosal (Merthiolate)
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注意事项
- Biohazard Informations: This product contains thimerosal which is hazardous.
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储存条件
- 4 °C/-20 °C
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储存方法
- Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
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- Fukutin (FKTN)
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别名
- fukutin
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背景
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The protein encoded by this gene is a putative transmembrane protein that is localized to the cis-Golgi compartment, where it may be involved in the glycosylation of alpha-dystroglycan in skeletal muscle.The encoded protein is thought to be a glycosyltransferase and could play a role in brain development.Defects in this gene are a cause of Fukuyama-type congenital muscular dystrophy (FCMD), Walker-Warburg syndrome (WWS), limb-girdle muscular dystrophy type 2M (LGMD2M), and dilated cardiomyopathy type 1X (CMD1X).Two transcript variants encoding the same protein have been found for this gene.[provided by RefSeq]
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分子量
- 54 kDa
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基因ID
- 2218
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NCBI登录号
- NM_006731, NP_006722
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途径
- Regulation of Carbohydrate Metabolic Process
抗原
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