ADAMTSL2 抗体 (AA 522-580) (Biotin)
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- 抗原 See all ADAMTSL2 抗体
- ADAMTSL2 (ADAMTS-Like 2 (ADAMTSL2))
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抗原表位
- AA 522-580
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适用
- 人
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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 ADAMTSL2 antibody is conjugated to Biotin
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应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 交叉反应
- 人
- 预测反应
- Mouse,Rat
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human ADAMTSL2
- 亚型
- IgG
- Top Product
- Discover our top product ADAMTSL2 Primary Antibody
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anti-ADAMTS-Like 2 (ADAMTSL2) (C-Term) antibody
ADAMTSL2 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500 - 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 μg/μL
- 缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C for 12 months.
- 有效期
- 12 months
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- 抗原
- ADAMTSL2 (ADAMTS-Like 2 (ADAMTSL2))
- 别名
- ADAMTSL2 (ADAMTSL2 产品)
- 别名
- ADAMTSL2 antibody, GPHYSD1 antibody, A930008K15Rik antibody, tcp-1 antibody, RGD1305459 antibody, ADAMTS-like 2 antibody, ADAMTS like 2 antibody, ADAMTS-like protein 2 antibody, ADAMTSL2 antibody, adamtsl2 antibody, LOC100589493 antibody, Adamtsl2 antibody
- 背景
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Synonyms: ADAMTS like 2, ADAMTS like protein 2, ADAMTS-like protein 2, ADAMTSL 2, ADAMTSL-2, ADAMTSL2, ATL2_HUMAN.
Background: ADAMTS (A Disintegrin And Metalloproteinase Domain with Thrombospondin type 1 Modules) is a family of zinc-dependent proteases that are implicated in a variety of normal and pathological conditions, including arthritis and cancer. ADAMTS protein family members contain an amino-terminal propeptide domain, a metalloproteinase domain, a disintegrin-like domain and a carboxy-terminus that contains a varying number of Thrombospondin type 1 (TSP-1) motifs. ADAMTS-L2 (ADAMTS-like protein 2) is a 951 amino acid secreted protein that is highly expressed in lung, kidney and liver. Mutations in the gene encoding ADAMTS are the cause of geleophysic dysplasia, an autosomal recessive disorder characterized by cardiac vavular anomalies, short stature, thick skin and brachydactyly. In individuals affected with geleophysic dysplasia, there is a significant increase in total active TGF-beta 1 and nuclear locations of p-SAMD2 in fibroblasts. Interestingly, ADAMTS-L2 interacts with LTBP-1, a glycoprotein that is part of the platelet-derived TGF-beta 1 complex.
- 基因ID
- 9719
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