中文 
别名:V-type proton ATPase subunit G 3, V-ATPase subunit G 3, V-ATPase 13 kDa subunit 3, Vacuolar proton pump subunit G 3, ATP6V1G3, ATP6G3应用:WB,ICC,FCM
反应种属:Human, Mouse
规格：50μl/100μl
| Description |
|---|
| Catalytic subunit of the peripheral V1 complex of vacuolar ATPase (V-ATPase). V-ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells. |
| Specification | |
|---|---|
| Aliases | V-type proton ATPase subunit G 3, V-ATPase subunit G 3, V-ATPase 13 kDa subunit 3, Vacuolar proton pump subunit G 3, ATP6V1G3, ATP6G3 |
| Entrez GeneID | 127124 |
| Swissprot | Q96LB4 |
| WB Predicted band size | 13.9kDa |
| Host/Isotype | Rabbit IgG |
| Storage | Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles. |
| Species Reactivity | Human, Mouse |
| Immunogen | This ATP6V1G3 antibody is generated from a rabbit immunized with a KLH conjugated synthetic peptide between 15-49 amino acids from the human region of human ATP6V1G3. |
| Application | |
|---|---|
| WB | 1/2000 |
| ICC | 1/25 |
| FCM | 1/25 |
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All lanes : Anti-ATP6V1G3 Antibody (N-Term) at 1:2000 dilution Lane 1: Human kidney lysate Lane 2: Caki-1 whole cell lysate Lane 3: Renca whole cell lysate Lane 4: Mouse kidney lysate Lysates/proteins at 20 µg per lane. Secondary Predicted band size : 14 kDa Blocking/Dilution buffer: 5% NFDM/TBST. |
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Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized U-2 OS (human osteosarcoma cell line) cells labeling ATP6V1G3 with P34539 at 1/25 dilution, followed by Dylight® 488-conjugated goat anti-rabbit IgG secondary antibody at 1/200 dilution (green). Immunofluorescence image showing cytoplasm and weak nucleus staining on U-2 OS cell line. Cytoplasmic actin is detected with Dylight® 554 Phalloidin at 1/100 dilution (red).The nuclear counter stain is DAPI (blue). |
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Overlay histogram showing U-2 OS cells stained with P34539(green line). The cells were fixed with 2% paraformaldehyde (10 min) and then permeabilized with 90% methanol for 10 min. The cells were then icubated in 2% bovine serum albumin to block non-specific protein-protein interactions followed by the antibody (P34539, 1:25 dilution) for 60 min at 37ºC. The secondary antibody used was Goat-Anti-Rabbit IgG, DyLight® 488 Conjugated Highly Cross-Adsorbed(OE188374) at 1/200 dilution for 40 min at 37ºC. Isotype control antibody (blue line) was rabbit IgG1 (1μg/1×10^6 cells) used under the same conditions. Acquisition of >10, 000 events was performed. |
本公司的所有产品仅用于科学研究或者工业应用等非医疗目的，不可用于人类或动物的临床诊断或治疗，非药用，非食用。
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本公司的所有产品仅用于科学研究或者工业应用等非医疗目的，不可用于人类或动物的临床诊断或治疗，非药用，非食用。
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