RPS24 抗体 (AA 83-133)
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- 抗原 See all RPS24 抗体
- RPS24 (Ribosomal Protein S24 (RPS24))
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抗原表位
- AA 83-133
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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 RPS24 antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunoprecipitation (IP)
- 原理
- Rabbit anti-RPS24 Antibody, Affinity Purified
- 预测反应
- Mouse,Rat,Golden hamster
- 纯化方法
- Affinity Purified
- 免疫原
- Between AA 83 and 133
- 亚型
- IgG
- Top Product
- Discover our top product RPS24 Primary Antibody
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anti-Ribosomal Protein S24 (RPS24) (AA 1-130) antibody
RPS24 适用: 人 WB, IHC, IP 宿主: 兔 Polyclonal unconjugated
anti-Ribosomal Protein S24 (RPS24) (AA 2-133) antibodyRPS24 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Ribosomal Protein S24 (RPS24) (AA 71-120) antibodyRPS24 适用: 人, 小鼠, 大鼠, 兔, Cow, 犬, 豚鼠, 马, 小鸡, Hamster, 猴, Pig, 非洲爪蟾 WB 宿主: 兔 Polyclonal unconjugated
anti-Ribosomal Protein S24 (RPS24) (AA 65-93) antibodyRPS24 适用: 人 WB, FACS 宿主: 兔 Polyclonal RB24304 unconjugated
anti-Ribosomal Protein S24 (RPS24) (Middle Region) antibodyRPS24 适用: 人, 小鼠, 大鼠, 兔, Cow, 犬, 豚鼠, 马, 斑马鱼 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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IP: 2 - 10 μg/mg lysate
WB: 1:2,000 - 1:10,000
- 限制
- 仅限研究用
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- 浓度
- 1000 μg/mL
- 缓冲液
- Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % Sodium Azide
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- 4 °C
- 有效期
- 12 months
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- 抗原
- RPS24 (Ribosomal Protein S24 (RPS24))
- 别名
- RPS24 (RPS24 产品)
- 别名
- DBA3 antibody, S24 antibody, ribosomal protein S24 L homeolog antibody, ribosomal protein S24 antibody, rps24.L antibody, RPS24 antibody, Rps24 antibody
- 背景
- Background: RPS24 (40S ribosomal protein S24) is a component of the 40S ribosomal subunit required for the processesing of pre-rRNA and maturation of the 40S ribosomal subunits. Defects in the RPS24 gene are the cause of Diamond-Blackfan anemia type 3 (DBA3) [MIM:610629]. DBA3 is a form of Diamond-Blackfan anemia, a congenital non-regenerative hypoplastic anemia that usually presents early in infancy. Diamond-Blackfan anemia is characterized by a moderate to severe macrocytic anemia, erythroblastopenia, and an increased risk of malignancy. 30 to 40 % of Diamond-Blackfan anemia patients present with short stature and congenital anomalies, the most frequent being craniofacial (Pierre-Robin syndrome and cleft palate), thumb and urogenital anomalies [taken from the Universal Protein Resource (UniProt) P62847].
- 基因ID
- 6229
- NCBI登录号
- NP_001017
- UniProt
- P62847
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