SLC26A4 抗体 (AA 250-350)
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- 抗原 See all SLC26A4 抗体
- SLC26A4 (Solute Carrier Family 26, Member 4 (SLC26A4))
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抗原表位
- AA 250-350
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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 SLC26A4 antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 原理
- SLC26A4 Rabbit pAb
- 序列
- VLSIIYTLVE IFQNIGDTNL ADFTAGLLTI VVCMAVKELN DRFRHKIPVP IPIEVIVTII ATAISYGANL EKNYNAGIVK SIPRGFLPPE LPPVSLFSEM L
- 交叉反应
- 小鼠
- 产品特性
- Polyclonal Antibodies
- 纯化方法
- Affinity purification
- 免疫原
- A synthetic peptide corresponding to a sequence within amino acids 250-350 of human SLC26A4 (NP_000432.1).
- 亚型
- IgG
- Top Product
- Discover our top product SLC26A4 Primary Antibody
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anti-Solute Carrier Family 26, Member 4 (SLC26A4) (AA 592-655) antibody
SLC26A4 适用: 人 ELISA, WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Solute Carrier Family 26, Member 4 (SLC26A4) (AA 674-754) antibodySLC26A4 适用: 人 ELISA, WB 宿主: 小鼠 Polyclonal unconjugated
anti-Solute Carrier Family 26, Member 4 (SLC26A4) (Middle Region) antibodySLC26A4 适用: 人, 大鼠, 小鼠, 兔, Cow, 犬, 豚鼠, 马 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Solute Carrier Family 26, Member 4 (SLC26A4) (AA 301-400) antibodySLC26A4 适用: 人, Pig ELISA, WB, IHC (p), IF (p), FACS 宿主: 兔 Polyclonal unconjugated
anti-Solute Carrier Family 26, Member 4 (SLC26A4) (AA 553-587) antibodySLC26A4 适用: 人, 大鼠 WB 宿主: 兔 Polyclonal RB53308 unconjugated
anti-Solute Carrier Family 26, Member 4 (SLC26A4) (AA 674-754) antibodySLC26A4 适用: 人 ELISA 宿主: 小鼠 Monoclonal 3D2 unconjugated
anti-Solute Carrier Family 26, Member 4 (SLC26A4) (Middle Region) antibodySLC26A4 适用: 人, 小鼠 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- WB,1:500 - 1:2000
- 限制
- 仅限研究用
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- 状态
- Liquid
- 缓冲液
- PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
- 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
- -20 °C
- 储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- 抗原
- SLC26A4 (Solute Carrier Family 26, Member 4 (SLC26A4))
- 别名
- SLC26A4 (SLC26A4 产品)
- 背景
- Mutations in this gene are associated with Pendred syndrome, the most common form of syndromic deafness, an autosomal-recessive disease. It is highly homologous to the SLC26A3 gene; they have similar genomic structures and this gene is located 3' of the SLC26A3 gene. The encoded protein has homology to sulfate transporters.,SLC26A4;DFNB4;EVA;PDS;TDH2B;pendrin,Cancer,Signal Transduction,Endocrine & Metabolism,Neuroscience,SLC26A4
- 分子量
- 39kDa/85kDa
- 基因ID
- 5172
- UniProt
- O43511
- 途径
- Thyroid Hormone Synthesis, Sensory Perception of Sound
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