SLC32A1 / VGAT Recombinant Mouse Monoclonal Antibody [PSH10-47] - BSA and Azide free
Catalog# HA610228
SLC32A1 / VGAT Recombinant Mouse Monoclonal Antibody [PSH10-47] - BSA and Azide free
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IHC-Fr
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IHC-P
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Mouse
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Rat
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HA601384
含抗保成分
-
Cynomolgus monkey
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Pig
予測される交差反応性
-
unconjugated
製品概要
製品名
SLC32A1 / VGAT Recombinant Mouse Monoclonal Antibody [PSH10-47] - BSA and Azide free
抗体のタイプ
Recombinant Mouse Monoclonal Antibody
交差反応性（対応種属）
Mouse, Rat (Predicted: Cynomolgus monkey, Pig)
予測される交差反応性
検証済みアプリケーション
IHC-Fr, IHC-P
標的分子量
Predicted band size: 57 kDa
ポジティブコントロール
Mouse brain tissue, mouse cerebellum tissue, rat brain tissue, rat cerebellum tissue.
コンジュゲーション
unconjugated
クローン番号
PSH10-47
製品の特徴
形態
Liquid
濃度
保存方法
Store at 2-8℃. Avoid freeze.
保存バッファー
1*PBS (pH7.4).
アイソタイプ
IgG1
精製方法
Protein A affinity purified.
推奨希釈倍率
ターゲット
機能
Vesicular inhibitory amino acid transporter is a protein that in humans is encoded by the SLC32A1 gene. The protein encoded by this gene is an integral membrane protein involved in gamma-aminobutyric acid (GABA) and glycine uptake into synaptic vesicles. The encoded protein is a member of amino acid/polyamine transporter family II.
背景・参考文献
1. Heron SE et al. Association of SLC32A1 Missense Variants With Genetic Epilepsy With Febrile Seizures Plus. Neurology. 2021 May
2. Guerrini R et al. SLC32A1: One More Gene Contributing to the Solution of the Genetic Generalized Epilepsies Mystery. Neurology. 2021 May
サブセルラー局在
Cytoplasmic vesicle membrane, Presynapse.
UNIPROT #
別名
bA122O1.1 antibody
GABA and glycine transporter antibody
hVIAAT antibody
SLC32A 1 antibody
Slc32a1 antibody
solute carrier family 32 (GABA vesicular transporter) member 1 antibody
Solute carrier family 32 member 1 antibody
Vesicular GABA Amino Acid Transporter antibody
Vesicular GABA transporter antibody
Vesicular inhibitory amino acid transporter antibody
詳細を見る画像
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This data was developed using HA601384, the same antibody clone in a different buffer formulation.
Application: IHC-Fr
Species: Mouse
Site: Cerebellum
Sample: Frozen section
Antibody concentration: 1:500 (SLC32A1 / VGAT, HA601384, green); 1:500 (Parvalbumin, ET1703-15, red)
Antigen retrieval: Not required -
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This data was developed using HA601384, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded mouse brain tissue with Mouse anti-SLC32A1 / VGAT antibody (HA601384) at 1/1,000 dilution.
The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA601384) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX. -
This data was developed using HA601384, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded mouse cerebellum tissue with Mouse anti-SLC32A1 / VGAT antibody (HA601384) at 1/1,000 dilution.
The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA601384) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX. -
This data was developed using HA601384, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded rat brain tissue with Mouse anti-SLC32A1 / VGAT antibody (HA601384) at 1/1,000 dilution.
The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA601384) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX. -
This data was developed using HA601384, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded rat cerebellum tissue with Mouse anti-SLC32A1 / VGAT antibody (HA601384) at 1/1,000 dilution.
The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA601384) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
ご注意: 本製品はすべて「研究用試薬」です。人や動物の診断・治療目的、または臨床診断には使用できません。（FOR RESEARCH USE ONLY）