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- 抗原 See all Laminin (LAMA2) 抗体
- Laminin (LAMA2) (Laminin, alpha 2 (LAMA2))
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抗原表位
- AA 152-170
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适用
- 人, 小鼠, 大鼠
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This Laminin antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 纯化方法
- Antigen affinity
- 免疫原
- Amino acids 152-170 (WILERSLDDVEYKPWQYHA-human) were used as the immunogen for this LAMA2 antibody (100% mouse homology).
- 亚型
- IgG
- Top Product
- Discover our top product LAMA2 Primary Antibody
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anti-Laminin, alpha 2 (LAMA2) (AA 3013-3122) antibody
LAMA2 适用: 人 ELISA, WB, IHC (p) 宿主: 小鼠 Monoclonal 2D4 unconjugated
anti-Laminin, alpha 2 (LAMA2) (AA 2051-2200) antibodyLAMA2 适用: 人, 小鼠, 大鼠, 马, Cow ELISA, IF (cc), IF (p), ICC, IHC (p), IHC (fro) 宿主: 兔 Polyclonal unconjugated
anti-Laminin, alpha 2 (LAMA2) (AA 2901-3106) antibodyLAMA2 适用: 小鼠 IHC, WB, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Laminin, alpha 2 (LAMA2) (AA 974-1162) antibodyLAMA2 适用: 人 ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Laminin, alpha 2 (LAMA2) (AA 2011-2060) antibodyLAMA2 适用: 人, 小鼠 ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- The stated application concentrations are suggested starting points. Titration of the LAMA2 antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 0.5-1 μg/mL
- 限制
- 仅限研究用
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- 缓冲液
- 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
- 储存条件
- -20 °C
- 储存方法
- After reconstitution, the LAMA2 antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
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- 抗原
- Laminin (LAMA2) (Laminin, alpha 2 (LAMA2))
- 别名
- LAMA2 Laminin 2 alpha (LAMA2 产品)
- 背景
- Laminin 2 alpha is a protein that in humans is encoded by the LAMA2 gene. This gene is mapped to 6q22.33. Laminin, an extracellular protein, is a major component of the basement membrane. It is though to mediate the attachment, migration, and organization of cells into tissues during embryonic development by interacting with other extracellular matrix components. It is composed of three subunits, alpha, beta, and gamma, which are bound to each other by disulfide bonds into a cross-shaped molecule. This gene encodes the alpha 2 chain, which constitutes one of the subunits of laminin 2 (merosin) and laminin 4 (s-merosin). Mutations in this gene have been identified as the cause of congenital merosin-deficient muscular dystrophy. Two transcript variants encoding different proteins have been found for this gene.
- UniProt
- P24043
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