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Abnova
SLC26A4 Monoclonal Antibody (3D2)
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产品信息
H00005172-M03
产品规格
种属反应
Human
宿主/亚型
Mouse
/ IgG2a, kappa
分类
Monoclonal
类型
Antibody
克隆号
3D2
抗原
SLC26A4 (NP_000432, 674 a.a. approximately 754 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
偶联物
形式
Liquid
浓度
See Label
纯化类型
Affinity chromatography
保存液
PBS, pH 7.4
内含物
no preservative
保存条件
-20°C, Avoid Freeze/Thaw Cycles
运输条件
Ambient (domestic); Wet ice (international)
产品详细信息
Sequence of this protein is as follows: RSLRVIVKEF QRIDVNVYFA SLQDYVIEKL EQCGFFDDNI RKDTFFLTVH DAILYLQNQV KSQEGQGSIL ETITLIQDCK D
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。
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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
