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Invitrogen
SLC26A4 Polyclonal Antibody
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产品信息
PA5-42060
应用
建议稀释比
已发表文章
产品规格
种属反应
Human
已发表种属
C. elegans,
Human,
Mouse
宿主/亚型
Rabbit
/ IgG
分类
Polyclonal
类型
Antibody
抗原
Synthetic peptide directed towards the middle region of human SLC26A4
偶联物
形式
Liquid
浓度
0.5 mg/mL
纯化类型
Affinity Chromatography
保存液
PBS with 2% sucrose
内含物
0.09% sodium azide
保存条件
-20°C, Avoid Freeze/Thaw Cycles
运输条件
Ambient (domestic); Wet ice (international)
RRID
产品详细信息
Peptide sequence: ELNDRFRHKI PVPIPIEVIV TIIATAISYG ANLEKNYNAG IVKSIPRGFL
Sequence homology: Cow: 92%; Dog: 100%; Guinea Pig: 100%; Horse: 93%; Human: 100%; Mouse: 100%; Rabbit: 100%; Rat: 92%
靶标信息
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.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
生物信息学
蛋白别名: Pendrin; Sodium-independent chloride/iodide transporter; solute carrier family 26 (anion exchanger), member 4; Solute carrier family 26 member 4; truncated solute carrier family 26
基因别名: DFNB4; EVA; PDS; SLC26A4; TDH2B
UniProt ID: (Human) O43511
Entrez Gene ID: (Human) 5172
chloride channel activity
secondary active sulfate transmembrane transporter activity
bicarbonate transmembrane transporter activity
chloride transmembrane transporter activity
iodide transmembrane transporter activity
sulfate transmembrane transporter activity
anion:anion antiporter activity
oxalate transmembrane transporter activity
transporter
ion transport
regulation of pH
sensory perception of sound
sulfate transport
inorganic anion transport
bicarbonate transport
iodide transport
oxalate transport
regulation of protein localization
regulation of membrane potential
regulation of intracellular pH
sulfate transmembrane transport
chloride transmembrane transport
