种属反应性Human,Mouse,Rat,Dog,Cow,Horse
验证应用WB,FC
抗体类型兔多抗
免疫原KLH conjugated synthetic peptide derived from human Legumain 201-300/433
偶联Non-conjugated
Anti-Legumain antibody性能
形态Liquid
浓度1 mg/mL.
存放说明Store at -20℃ for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20℃. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4℃.
存储缓冲液0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
亚型IgG
纯化方式affinity purified by Protein A
亚细胞定位Lysosome (By similarity).
数据链接SwissProt: Q99538 Human
其它名称AEP
Asparaginyl endopeptidase
EC 3.4.22.34
LGMN
LGMN1
Protease, cysteine 1
protease, cysteine, 1 (legumain)
PRSC1
LGMN_HUMAN.
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Anti-Legumain antibody应用
WB:1:500-2000
FC:3ug/Test
Fig1: Overlay histogram showing Mouse spleen cells stained with ER1912-26-PE (red line). The cells were fixed with 1% paraformaldehyde (10 min).The cells were then incubated with the antibody (ER1912-26-PE, 2ug/1x106cells) for 30 min at 22-25℃. Isotype control antibody (black line) was rabbit IgG (2ug/1x106cells) used under the same conditions. Acquisition of events were used for analysis.
Fig2: Sample: Kidney (Mouse) Lysate at 40 ug
Primary: Anti- Legumain (ER1912-26) at 1/300 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 46 kD
Observed band size: 55 kD
Fig3: Sample: Placenta (Mouse) Lysate at 40 ug
Primary: Anti-Legumain (ER1912-26) at 1/300 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 46 kD
Observed band size: 55 kD
Fig4: Blank control: HL60. Primary Antibody (green line): Rabbit Anti-Legumain antibody (ER1912-26) Dilution: 3μg /10^6 cells; Isotype Control Antibody (orange line): Rabbit IgG . Secondary Antibody : Goat anti-rabbit IgG-PE Dilution: 1μg /test. Protocol The cells were fixed with 4% PFA (10min at room temperature)and then permeabilized with PBST for 20 min at room temperature. The cells were then incubated in 5%BSA to block non-specific protein-protein interactions for 30 min at at room temperature .Cells stained with Primary Antibody for 30 min at room temperature. The secondary antibody used for 40 min at room temperature. Acquisition of 20,000 events was performed.
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