UROD 抗体 (N-Term)
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- 抗原 See all UROD 抗体
- UROD (Uroporphyrinogen Decarboxylase (UROD))
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抗原表位
- N-Term
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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 UROD antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunohistochemistry (IHC)
- 特异性
- UROD antibody was raised against the N terminal of UROD
- 纯化方法
- Purified
- 免疫原
- UROD antibody was raised using the N terminal of UROD corresponding to a region with amino acids SLLLLLFLFIVIFALLGMQLFGGRYDFEDTEVRRSNFDNFPQALISVFQV
- Top Product
- Discover our top product UROD Primary Antibody
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- 应用备注
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WB: 2.5 µg/mL, IHC: 4-8 µg/mL
Optimal conditions should be determined by the investigator. - 说明
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UROD Blocking Peptide, catalog no. 33R-8607, is also available for use as a blocking control in assays to test for specificity of this UROD 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 UROD 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
- UROD (Uroporphyrinogen Decarboxylase (UROD))
- 别名
- UROD (UROD 产品)
- 别名
- UROD antibody, pct antibody, wu:fc43e09 antibody, PCT antibody, UPD antibody, AI323803 antibody, Uro-d antibody, porphyrinogen carboxy-lyase antibody, uroporphyrinogen decarboxylase antibody, Uroporphyrinogen decarboxylase UroD antibody, Uroporphyrinogen decarboxylase antibody, UROD antibody, urod antibody, hemE antibody, uroD antibody, Cpin_6502 antibody, Rmar_1187 antibody, LOC5568261 antibody, Mrub_1403 antibody, Arnit_2230 antibody, Ndas_2830 antibody, Mesil_2989 antibody, Trad_0222 antibody, Weevi_0432 antibody, Hipma_1229 antibody, Fluta_0529 antibody, Marky_1143 antibody, Halhy_5610 antibody, Mesop_0899 antibody, Ccan_20670 antibody, Urod antibody
- 背景
- UROD is the fifth enzyme of the heme biosynthetic pathway. This enzyme is responsible for catalyzing the conversion of uroporphyrinogen to coproporphyrinogen through the removal of four carboxymethyl side chains. Mutations and deficiency in this enzyme are known to cause familial porphyria cutanea tarda and hepatoerythropoetic porphyria.
- 分子量
- 40 kDa (MW of target protein)
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