Membrane transport protein XK (XK) (N-Term) 抗体
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- 抗原 See all Membrane transport protein XK (XK) 抗体
- Membrane transport protein XK (XK)
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抗原表位
- N-Term
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适用
- 人, 小鼠, 大鼠, 兔, 犬, Cow, 豚鼠, 马, Pig
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- 非结合性
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应用范围
- Western Blotting (WB)
- 序列
- QMPKNGLSEE IEKEVGQAEG KLITHRSAFS RASVIQAFLG SAPQLTLQLY
- 预测反应
- Cow: 92%, Dog: 92%, Guinea Pig: 85%, Horse: 85%, Human: 100%, Mouse: 85%, Pig: 100%, Rabbit: 100%, Rat: 100%
- 产品特性
- This is a rabbit polyclonal antibody against XK. It was validated on Western Blot using a cell lysate as a positive control.
- 纯化方法
- Affinity Purified
- 免疫原
- The immunogen is a synthetic peptide directed towards the N terminal region of human XK
- Top Product
- Discover our top product XK Primary Antibody
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- 应用备注
- Optimal working dilutions should be determined experimentally by the investigator.
- 说明
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Antigen size: 444 AA
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- Lot specific
- 缓冲液
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
- 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.
- 注意事项
- Avoid repeated freeze-thaw cycles.
- 储存条件
- -20 °C
- 储存方法
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
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- 抗原
- Membrane transport protein XK (XK)
- 别名
- XK (XK 产品)
- 别名
- KX antibody, MCLDS antibody, X1k antibody, XKR1 antibody, XRG1 antibody, 1810038K19Rik antibody, Xkh antibody, X-linked Kx blood group antibody, XK antibody, Xk antibody
- 背景
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This locus controls the synthesis of the Kell blood group 'precursor substance' (Kx). Mutations in this gene have been associated with McLeod syndrome, an X-linked, recessive disorder characterized by abnormalities in the neuromuscular and hematopoietic systems. XK has structural characteristics of prokaryotic and eukaryotic membrane transport proteins. This locus controls the synthesis of the Kell blood group 'precursor substance' (Kx). Mutations in this gene have been associated with McLeod syndrome, an X-linked, recessive disorder characterized by abnormalities in the neuromuscular and hematopoietic systems. The encoded protein has structural characteristics of prokaryotic and eukaryotic membrane transport proteins. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Alias Symbols: KX, X1k, XKR1, MCLDS
Protein Interaction Partner: CARD6, NLRC4, INPPL1, CASP1, CLGN, ELAVL1, PRKCA, CSNK2A1, KEL, DYT10,
Protein Size: 444 - 分子量
- 51 kDa
- 基因ID
- 7504
- NCBI登录号
- NM_021083, NP_066569
- UniProt
- P51811
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