抗VR1/ TRPV1抗体 | Anti-VR1/ TRPV1 antibody

掲載日情報:2020/04/02 現在Webページ番号:146922

GeneTex社の抗VR1/ TRPV1抗体 | Anti-VR1/ TRPV1 antibodyです。

本製品は研究用です。研究用以外には使用できません。

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

[在庫・価格 :2024年06月17日 20時55分現在]

※ 表示されている納期は弊社に在庫が無く、取り寄せた場合の納期目安となります。
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納期 文献数
Anti-VR1 C-terminus antibody, Guinea Pig-Poly
2~3週間 ※ 表示されている納期は弊社に在庫がなく、取り寄せた場合の目安納期となります。 0
説明文
別名:transient receptor potential cation channel,subfamily V,member 1,TRPV1_SON,VR.5'sv,Vr1,Vr1l1
Genbank No: 83810
法規制等
保存条件 -20℃ 法規備考
抗原種 Rat 免疫動物 Guinea Pig クラス IgG 標識 Unlabeled
交差性 Human/Mouse/Rat 適用 IHC
クロナリティ Polyclonal フォーマット 性状 Purified 吸収処理
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製品記事
関連記事 GeneTex社における抗体の品質管理

[在庫・価格 :2024年06月17日 20時55分現在]

※ 表示されている納期は弊社に在庫が無く、取り寄せた場合の納期目安となります。

Anti-VR1 C-terminus antibody, Guinea Pig-Poly

文献数: 0

説明文 別名:transient receptor potential cation channel,subfamily V,member 1,TRPV1_SON,VR.5'sv,Vr1,Vr1l1
Genbank No: 83810
法規制等
保存条件 -20℃ 法規備考
抗原種 Rat 免疫動物 Guinea Pig
交差性 Human/Mouse/Rat 適用 IHC
標識 Unlabeled 性状 Purified
吸収処理 クラス IgG
クロナリティ Polyclonal フォーマット
掲載カタログ

製品記事
関連記事 GeneTex社における抗体の品質管理



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DATA IMAGES

VR1-C staining of rat dorsal horn (dilution 1:100).
TRPV1 staining of mouse inferior olive using Cy3-conjugated donkey anti-rabbit secondary antibodies (red color) and DAPI (blue) as a nuclear counterstain.
Evaluation of the expression patterns of TLR4 and CD14 in trigeminal sensory neurons. White arrows depict examples of neurons expressing both markers for each row of three images, and yellow arrows depict examples of neurons that express one but not both markers. Human trigeminal neurons were evaluated for co-localization of TLR4 (Panels A,D), CD14 (Panel B), with a marker for the capsaicinsensitive subclass of nociceptors (TRPV1, Panels B,C for TLR4 and Panels K,L for CD14), or a marker of myelinated sensory neurons (N52, Panels Figure 1. Evaluation of the expression patterns of TLR4 and CD14 in trigeminal sensory neurons. White arrows depict examples of neurons expressing both markers for each row of three images, and yellow arrows depict examples of neurons that express one but not both markers. Human trigeminal neurons were evaluated for co-localization of TLR4 (Panels A,D), CD14 (Panel J), with a marker for the capsaicinsensitive subclass of nociceptors (TRPV1, Panels B,C for TLR4 and Panels K,L for CD14), or a marker of myelinated sensory neurons (N52, Panels E,F). Rat trigeminal neurons were evaluated for co-localization of TLR4 with TRPV1 (Panels G-I) and CD14 with TRPV1 (Panels M-O). The addition of blocking peptide or the deletion of primary or secondary antisera produced a complete loss of signal in both the human and rat tissues. Scale bar is 100 um for Panels A-F and J-L, and 200 um for Panels G-I and M-O. Rat trigeminal neurons were evaluated for co-localization of TLR4 with TRPV1 (Panels G-I) and CD14 with TRPV1 (Panels M-O). The addition of blocking peptide or the deletion of primary or secondary antisera produced a complete loss of signal in both the human and rat tissues. Scale bar is 100 um for Panels A-F and J-L, and 200 um for Panels G-I and M-O


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製品情報

HostGuinea pig
ClonalityPolyclonal
ApplicationICC/IF, IHC
ReactivityHuman, Mouse, Rat


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APPLICATION

Application Note

For IHC: Use at a dilution of 1:1,000. Optimal dilutions/concentrations should be determined by the researcher. Immunohistochemistry: Antiserum was used on perfusion fixed tissue. Perfusion: 1) calcium-free Tyrode’s solution, 2) 4% paraformaldehyde fixative, and 3) 10% sucrose in PBS as a cryo-protectant. Desired tissues were dissected and stored overnight in 10% sucrose in PBS. Slide-mounted tissue sections were processed for indirect immunofluorescence. Slides were incubated with blocking buffer for 1 hour at room temperature. Primary antiserum was diluted with blocking buffer to the appropriate working concentration. Blocking buffer was removed and slides were incubated for 18-24 hours at 4oC with primary antiserum. Slides were rinsed 3 times and then incubated with secondary antibodies for 1 hour at room temperature. Slides were again rinsed 3 times and coverslipped. Staining was examined using fluorescence microscopy. Note: Sodium azide (NaN3) interferes with peroxidase reactions and should not be used with peroxidase methodologies. If sodium azide is present in any steps of the staining procedure, the tissue should thoroughly be rinsed with sodium azide-free buffer before performing the peroxidase reaction.

Calculated MW 95 kDa. ( Note )


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PROPERTIES

Form Liquid
Buffer Contains 0.05% 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.
Antigen Species Rat
Immunogen YTGSLKPEDAEVFKDSMVPGEK Corresponding to residues of the carboxy-terminus of rat VR1
Purification Unpurified
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 Transient Receptor Potential Cation Channel, Subfamily V, Member 1 , Trpv1_Son , Vr.5'Sv , Vr1 , Vr1L1 , Trpv1
Background VR1 (vanilloid receptor 1) is a channel activated by capsaicin, the pungent ingredient in hot peppers. It was isolated from sensory neurons. Sequence analysis suggests that VR1 has six transmembrane domains and intracellular N- and C-termini. It shares structural similarities with the family of putative store-operated calcium channels. VR1 is expressed by nociceptive sensory neurons. It is activated by noxious heat and is thought to function as transducer of noxious thermal stimuli.
Database ・ Gene ID: 83810
・ UniProt: O35433


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お問い合わせ先

(テクニカルサポート 試薬担当)

reagent@funakoshi.co.jp

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