Fukutin 抗体 (Middle Region)
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北京 101111
Quick Overview for Fukutin 抗体 (Middle Region) (ABIN952403)
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 184-214, Middle Region
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特异性
- This antibody recognizes Human and Mouse FKTN (Center).
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纯化方法
- Protein A column, followed by peptide affinity purification
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免疫原
- KLH conjugated synthetic peptide between 184-214 amino acids from the Central region of Human Fukutin. Genename: FKTN
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亚型
- Ig Fraction
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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) antibodyFKTN 适用: 人 WB, IHC 宿主: 兔 Monoclonal 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 (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
- Optimal working dilution should be determined by the investigator.
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 0.25 mg/mL
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缓冲液
- PBS containing 0.09 % (W/V) Sodium Azide as preservative
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储存液
- Sodium azide
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注意事项
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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注意事项
- Avoid repeated freezing and thawing.
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储存条件
- 4 °C/-20 °C
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储存方法
- Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
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- Fukutin (FKTN)
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别名
- Fukutin
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背景
- 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). Alternatively spliced transcript variants have been found for this gene.Synonyms: FCMD, FKTN, Fukuyama-type congenital muscular dystrophy protein
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分子量
- 53724 Da
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基因ID
- 2218
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NCBI登录号
- NP_001073270
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途径
- Regulation of Carbohydrate Metabolic Process
抗原
-
