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Invitrogen
GPD1L Polyclonal Antibody
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GPD1L Antibody (PA5-114389) in WB
Western blot analysis of GPD1L in the following samples: Lane 1: human placenta issue lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: human U-87MG whole cell lysates, Lane 4: human HL-60 whole cell lysates, Lane 5: human HepG2 whole cell lysates, Lane 6: human A549 whole cell lysates, Lane 7: human Caco-2 whole cell lysates, Lane 8: human K562 whole cell lysates, Lane 9: rat heart issue lysates, Lane 10: mouse RAW246.7 whole cell lysates. Samples consisting of 50 µg (reducing conditions) of protein was separated with 5-20% SDS-PAGE... View More
Please note: We are reviewing Western blot images included in the antibody testing data in our catalog, including those provided by third parties. Unless expressly labeled or annotated as “raw-unedited”, Western blot images included in the antibody testing data in our catalog may have been edited, optimized or otherwise adjusted for presentation.
产品信息
PA5-114389
产品规格
种属反应
Human,
Mouse,
Rat
宿主/亚型
Rabbit
/ IgG
分类
Polyclonal
类型
Antibody
抗原
E.coli-derived human GPD1L recombinant protein (Position: A19-T351).
偶联物
Unconjugated
Unconjugated
Unconjugated
形式
Lyophilized
浓度
500 µg/mL
规格
100 µg
纯化类型
Affinity chromatography
保存液
PBS with 4mg trehalose
内含物
0.05mg sodium azide
保存条件
-20°C
运输条件
Ambient (domestic); Wet ice (international)
RRID
产品详细信息
Reconstitute with 0.2 mL of distilled water to yield a concentration of 500 µg/mL.
Positive Control - WB: human placenta issue, human PC-3 whole cell, human U-87MG whole cell, human HL-60 whole cell, human HepG2 whole cell, human A549 whole cell, human Caco-2 whole cell, human K562 whole cell, rat heart issue, mouse RAW2467 whole cell.|Store at -20°C for one year from date of receipt. After reconstitution, at 4°C for one month. It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freeze-thaw cycles.
靶标信息
The protein encoded by this gene catalyzes the conversion of sn-glycerol 3-phosphate to glycerone phosphate. The encoded protein is found in the cytoplasm, associated with the plasma membrane, where it binds the sodium channel, voltage-gated, type V, alpha subunit (SCN5A). Defects in this gene are a cause of Brugada syndrome type 2 (BRS2) as well as sudden infant death syndrome (SIDS).
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: Glycerol-3-phosphate dehydrogenase 1-like protein; GPD1-L
基因别名: 2210409H23Rik; D9Ertd660e; GPD1L; KIAA0089; RGD1560123
UniProt ID: (Mouse) Q3ULJ0
Entrez Gene ID: (Mouse) 333433, (Rat) 363159
regulation of heart rate
carbohydrate metabolic process
glycerol-3-phosphate metabolic process
NADH metabolic process
positive regulation of sodium ion transport
NAD metabolic process
negative regulation of peptidyl-serine phosphorylation
glycerol-3-phosphate catabolic process
oxidation-reduction process
regulation of ventricular cardiac muscle cell membrane depolarization
ventricular cardiac muscle cell action potential
negative regulation of protein kinase C signaling
positive regulation of protein localization to cell surface
regulation of sodium ion transmembrane transporter activity
biological_process
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Clicking the images or links will redirect you to a website hosted by BenchSci that provides third-party scientific content. Neither the content nor the BenchSci technology and processes for selection have been evaluated by us; we are providing them as-is and without warranty of any kind, including for use or application of the Thermo Fisher Scientific products presented.
