抗Dopamine Receptor D2抗体 | Anti-Dopamine Receptor D2 antibody

• 特長
• 価格
• DATA IMAGES
• 製品情報
• APPLICATION
• PROPERTIES
• TARGET

特長

• 高品質の抗体です。
• 幅広い研究分野に関連する抗体を取り揃えています。
• 使用されたアプリケーションや動物種などの情報が充実しています。
• 多数の論文で使用実績がある信頼性の高い抗体です。

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価格

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DATA IMAGES

IHC-P analysis of human brain tissue (neurons and glia) using GTX71747 Dopamine Receptor D2 antibody.Antigen retrival : Heat-induced antigen retrieval

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製品情報

Host	Rabbit
Clonality	Polyclonal
Isotype	IgG
Application	IHC-P
Reactivity	Human

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APPLICATION

Application Note

*Optimal dilutions/concentrations should be determined by the researcher.

Application	Dilution
IHC-P	10 μg/ml

Not tested in other applications.

Calculated MW	51 kDa. ( Note )
Predict Reactivity	Rabbit, Bovine, Dog, Pig, Monkey, Bat, Chimpanzee, Elephant, Ferret, Gibbon, Gorilla, Horse, Marmoset, Panda(>80% identity)

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PROPERTIES

Form	Liquid
Buffer	PBS, 0.1% sodium azide
Storage	Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4ºC. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.
Concentration	1 mg/ml (Please refer to the vial label for the specific concentration.)
Antigen Species	Human
Immunogen	Synthetic 16 amino acid peptide from 3rd cytoplasmic domain of human Dopamine Receptor D2.
Purification	Purified by affinity chromatography
Conjugation	Unconjugated
Note	For laboratory use only. Not for any clinical, therapeutic, or diagnostic use in humans or animals. Not for animal or human consumption.

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TARGET

Synonyms	dopamine receptor D2 , D2DR , D2R
Cellular Localization	Cell membrane
Background	This gene encodes the D2 subtype of the dopamine receptor. This G-protein coupled receptor inhibits adenylyl cyclase activity. A missense mutation in this gene causes myoclonus dystonia; other mutations have been associated with schizophrenia. Alternative splicing of this gene results in two transcript variants encoding different isoforms. A third variant has been described, but it has not been determined whether this form is normal or due to aberrant splicing. [provided by RefSeq, Jul 2008]
Database	・ Gene ID: 1813 DRD2 ・ UniProt: P14416 DRD2

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