COL1A2 抗体 (Middle Region)
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- 抗原 See all COL1A2 抗体
- COL1A2 (Collagen, Type I, alpha 2 (COL1A2))
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抗原表位
- Middle Region
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适用
- 人, 小鼠, 大鼠, 犬, 兔, Cow, 小鸡, 非洲爪蟾
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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 COL1A2 antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 特异性
- Collagen Type I alpha 2 antibody was raised against the middle region of COL1 A2
- 纯化方法
- Affinity purified
- 免疫原
- Collagen Type I alpha 2 antibody was raised using the middle region of COL1 A2 corresponding to a region with amino acids PGSVGPAGPRGPAGPSGPAGKDGRTGHPGTVGPAGIRGPQGHQGPAGPPG
- Top Product
- Discover our top product COL1A2 Primary Antibody
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- 应用备注
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WB: 1 µg/mL
Optimal conditions should be determined by the investigator. - 说明
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Collagen Type I alpha 2 Blocking Peptide, catalog no. 33R-7134, is also available for use as a blocking control in assays to test for specificity of this Collagen Type I alpha 2 antibody
- 限制
- 仅限研究用
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- 状态
- Lyophilized
- 溶解方式
- Lyophilized powder. Add distilled water for a 1 mg/mL concentration of COL0 2 antibody in PBS
- 浓度
- Lot specific
- 缓冲液
- PBS
- 注意事项
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Avoid repeated freeze/thaw cycles.
Dilute only prior to immediate use. - 储存条件
- 4 °C/-20 °C
- 储存方法
- Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
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- 抗原
- COL1A2 (Collagen, Type I, alpha 2 (COL1A2))
- 别名
- Collagen Type I alpha 2 (COL1A2 产品)
- 别名
- AA960264 antibody, AI325291 antibody, Col1a-2 antibody, Cola-2 antibody, Cola2 antibody, oim antibody, OI4 antibody, Gas-6 antibody, alpha2(I) antibody, hm:zehn2357 antibody, wu:fa98d05 antibody, wu:fa99g10 antibody, wu:fb04c08 antibody, wu:fb11d06 antibody, zehn2357 antibody, coagulation factor II, thrombin antibody, collagen, type I, alpha 2 antibody, collagen type I alpha 2 chain antibody, collagen type I alpha 2 L homeolog antibody, growth arrest specific 6 antibody, F2 antibody, Col1a2 antibody, col1a2.L antibody, COL1A2 antibody, Gas6 antibody, col1a2 antibody
- 背景
- COL1A2 is the pro-alpha2 chain of type I collagen whose triple helix comprises two alpha1 chains and one alpha2 chain. Type I is a fibril-forming collagen found in most connective tissues and is abundant in bone, cornea, dermis and tendon. Mutations in this gene are associated with osteogenesis imperfecta types I-IV, Ehlers-Danlos syndrome type VIIB, recessive Ehlers-Danlos syndrome Classical type, idiopathic osteoporosis, and atypical Marfan syndrome. Symptoms associated with mutations in this gene, however, tend to be less severe than mutations in the gene for the alpha1 chain of type I collagen (COL1A1) reflecting the different role of alpha2 chains in matrix integrity.
- 分子量
- 150 kDa (MW of target protein)
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