SLFN12 抗体 (C-Term)
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Quick Overview for SLFN12 抗体 (C-Term) (ABIN500746)
抗原
适用
宿主
克隆类型
标记
应用范围
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抗原表位
- C-Term
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交叉反应 （详细）
- Species reactivity (tested):Human
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纯化方法
- Peptide affinity chromatography
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免疫原
- SLFN12 antibody was raised against a 12 amino acid peptide from near the carboxy terminus human SLFN12.
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亚型
- IgG
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anti-Schlafen Family Member 12 (SLFN12) (C-Term) antibody
SLFN12 适用: 人 WB, IHC (p), EIA 宿主: 兔 Polyclonal unconjugated
anti-Schlafen Family Member 12 (SLFN12) (N-Term) antibodySLFN12 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Schlafen Family Member 12 (SLFN12) (AA 35-84) antibodySLFN12 适用: 人, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Schlafen Family Member 12 (SLFN12) (AA 192-220) antibodySLFN12 适用: 人 WB 宿主: 兔 Polyclonal RB31782 unconjugated
anti-Schlafen Family Member 12 (SLFN12) (C-Term) antibodySLFN12 适用: 人 WB, ELISA, IHC (p) 宿主: 兔 Polyclonal unconjugated
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应用备注
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ELISA. Western blot: 1 - 2 μg/mL.
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user. -
限制
- 仅限研究用
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浓度
- 1.0 mg/mL
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缓冲液
- PBS containing 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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注意事项
- Avoid repeated freezing and thawing.
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储存条件
- -20 °C
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储存方法
- Store the antibody (in aliquots) at -20 °C.
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- SLFN12 (Schlafen Family Member 12 (SLFN12))
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别名
- SLFN12
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背景
- Despite being first described several years ago, the roles of the Schlafen (SLFN) family of proteins remain largely unknown. The SLFN genes are preferentially expressed in lymphoid tissues and differentially regulated during thymocyte maturation. It is thought that many play roles in cell growth, hemopoietic cell differentiation, and T cell development and maturation. Most members contain at least one divergent AAA domain (AAA_4) that may play a role in ATP binding. Although also known as SLFN3, a Schlafen family member that may be a marker of T cell activation, human SLFN12 has relatively low homology to SLFN3 in other species. Loss of the SLFN12 gene due to deletion is associated with Kabuki syndrome, a multiple congenital anomaly syndrome, suggesting SLFN may play a role in this genetic condition.Synonyms: Schlafen 12, Schlafen family member 12, Schlafen12
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基因ID
- 55106
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NCBI登录号
- NP_060512
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UniProt
- Q8IYM2
抗原
-
