MFAP1 抗体 (AA 83-437) (FITC)
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Quick Overview for MFAP1 抗体 (AA 83-437) (FITC) (ABIN8009952)
抗原
See all MFAP1 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 83-437
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原理
- Anti-MFAP1 Antibody FITC Conjugated
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交叉反应 （详细）
- No cross-reactivity with other proteins.
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纯化方法
- Immunogen affinity purified.
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免疫原
- E.coli-derived human MFAP1 recombinant protein (Position: D83-K437).
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亚型
- IgG
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anti-Microfibrillar Associated Protein 1 (MFAP1) (AA 31-120) antibody
MFAP1 适用: 人, 小鼠 WB, ELISA, IF (cc), IF (p), IHC (fro), IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Microfibrillar Associated Protein 1 (MFAP1) (AA 175-225) antibodyMFAP1 适用: 人, 小鼠 WB, IP 宿主: 兔 Polyclonal unconjugated
anti-Microfibrillar Associated Protein 1 (MFAP1) (AA 21-50), (N-Term) antibodyMFAP1 适用: 人 WB 宿主: 兔 Polyclonal RB09350 unconjugated
anti-Microfibrillar Associated Protein 1 (MFAP1) (AA 61-110) antibodyMFAP1 适用: 人, 小鼠, 大鼠, Cow, 犬, 豚鼠, 马, 兔, Bat, Hamster, 猴, Pig WB 宿主: 兔 Polyclonal unconjugated
anti-Microfibrillar Associated Protein 1 (MFAP1) (C-Term) antibodyMFAP1 适用: 人, 小鼠, 大鼠, Cow, 犬, 豚鼠, 马, 兔, Bat, Hamster, 猴, Pig, 小鸡 WB 宿主: 兔 Polyclonal unconjugated
anti-Microfibrillar Associated Protein 1 (MFAP1) (Middle Region) antibodyMFAP1 适用: 人, 小鼠, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- Flow Cytometry, Optimal dilutions should be determined by end users.
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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
- Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % 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
- -20 °C
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储存方法
- At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.
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有效期
- 12 months
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- MFAP1 (Microfibrillar Associated Protein 1 (MFAP1))
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别名
- MFAP1
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背景
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Background: Microfibrillar-associated protein 1 is a protein that in humans is encoded by the MFAP1 gene. Microfibrils are an important component of the extracellular matrix of many tissues and can either associate with or without elastin. Several microfibril associated proteins (MFAPs) have been cloned, including MFAP1, MFAP3 and MFAP4. The MFAP1 and MFAP3 genes are localized near the fibrillin genes FBN1 and FBN2, respectively. Mutations in FBN1 are linked to Marfan syndrome. Mutations in FBN2 have been linked to congenital contractural arachnodactyly. This suggests roles for MFAP1 and MFAP3 in heritable diseases affecting microfibrils. Deletion of MFAP4 was found in 30 of 31 patients with Smith-Magenis syndrome (SMS), a clinically recognizable multiple congenital anomaly/mental retardation syndrome
Gene Full Name: microfibril associated protein 1
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基因ID
- 4236
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UniProt
- P55081
抗原
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