Fukutin 抗体 (AA 177-206)
Quick Overview for Fukutin 抗体 (AA 177-206) (ABIN656713)
抗原
See all Fukutin (FKTN) 抗体适用
宿主
克隆类型
标记
应用范围
克隆位点
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抗原表位
- AA 177-206
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预测反应
- Pr
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纯化方法
- This antibody is purified through a protein A column, followed by peptide affinity purification.
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免疫原
- This FKTN antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 177-206 amino acids from the Central region of human 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) (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) (N-Term) antibodyFKTN 适用: 人, 小鼠, 大鼠, 犬, 马, 兔, 豚鼠, Cow, Pig WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Fukutin (FKTN) (AA 184-214), (Middle Region) antibodyFKTN 适用: 人, 小鼠 WB, IHC (p), EIA 宿主: 兔 Polyclonal unconjugated
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应用备注
- WB: 1:1000. IHC-P: 1:10~50
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限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
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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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储存条件
- 4 °C,-20 °C
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储存方法
- FKTN Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.
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有效期
- 6 months
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- Fukutin (FKTN)
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别名
- FKTN
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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.
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分子量
- 53724
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基因ID
- 2218
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NCBI登录号
- NP_001073270, NP_001185892, NP_006722
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UniProt
- O75072
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途径
- Regulation of Carbohydrate Metabolic Process
抗原
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