Tag HA Antibodi Monoklonal Kelinci (ARA782)
WB | 1:1000-1:2000 |
JIKA/ICC | 1:400-1:2000 |
FC | 1:400-1:2000 |
IP | 1:10 |
Deskripsi | Antibodi Monoklonal Kelinci terhadap tag HA |
Tipe Antibodi | Antibodi primer |
Prediksi UM | |
Imunogen | YPYDVPDYA (influenza hemagglutinin-HA-epitope) terkonjugasi ke KLH. |
Pemurnian | IgG murni afinitas ProA |
Formulir/Penyangga | PBS 59%, Natrium azida 0,01%, Gliserol 40%, BSA 0,57%. |
Nama Alternatif | tag epitop HA; hemaglutinin |
*Clone Number, Reactivity, Source/Host and Clonality can be found in the product name and Key Features section above.

Prediksi UM: Tergantung pada protein fusi dengan tag HA
Lane 1: 293 cells lysate transfected with C-terminal HA tagged gene (ARA782 at 1:2,000 dilution).
Lane 2: 293 cells lysate transfected with N-terminal HA tagged gene (ARA782 at 1:1,000 dilution).
Jalur 3: 293 sel lisat tanpa transfeksi apa pun (ARA782 pada pengenceran 1:400).
Jalur 1: 1 µg per jalur
Jalur 2/3: 10 µg per jalur
Ab ke-2:
GAR HRP(H+L) 1:5.000
Paparan: 20 detik

Overlay histogram showing 293 cells transfected with N-terminal (Green) and C-terminal (Red) HA tagged gene stained with ARA782. The cells were then incubated in the antibody (ARA782, 1:2,000 dilution) in 1x PBS/1% BSA for 30 min at room temperature. The secondary antibody used was a Goat Anti-Rabbit Alexa Fluor® 488 (IgG H+L) at 1:2,000 dilution for 20 min at room temperature. Unlabelled sample (Black) was used as a control.

ARA782 staining HA tag in 293 cells transfected with N-terminal HA tagged gene by IF/ICC (immunofluorescence/immunocytochemistry). Cells were fixed with paraformaldehyde, permeabilized with 0.1% Triton X-100 and blocked with 10% goat serum for half an hour at room temperature. Samples were incubated with primary antibody (1:2,000) at 4°C. An Alexa Fluor® 594-conjugated Goat Anti-Rabbit IgG polyclonal was used as the secondary antibody (1:500). DAPI (blue) was used as the nuclear counter stain.
Control: PBS and secondary antibody, An Alexa Fluor® 594-conjugated Goat Anti-Rabbit IgG (1:500).

ARA782 staining HA tag in 293 cells transfected with C-terminal HA tagged gene by IF/ICC (immunofluorescence/immunocytochemistry). Cells were fixed with paraformaldehyde, permeabilized with 0.1% Triton X-100 and blocked with 10% goat serum for half an hour at room temperature. Samples were incubated with primary antibody (1:2,000) at 4°C. An Alexa Fluor® 594-conjugated Goat Anti-Rabbit IgG polyclonal was used as the secondary antibody (1:500). DAPI (blue) was used as the nuclear counter stain.
Control: PBS and secondary antibody, An Alexa Fluor® 594-conjugated Goat Anti-Rabbit IgG (1:500).

HA tag was immunoprecipitated from 0.2mg of 293 whole cells lysate transfected with N-terminal HA tagged gene with ARA782 at 1:10 dilution.
Ab ke-2:
GAR HRP untuk IP 1:500
Jalur 1: IP ARA782 dalam 293 lisat sel utuh ditransfeksi dengan gen bertanda N-terminal HA
Lane 2: PBS instead of ARA782 in 293 whole cell lysate transfected with N-terminal HA tagged gene
Jalur 3: 293 lisat sel utuh ditransfeksi dengan gen bertanda N-terminal HA, 10 µg (input)
Paparan: 60an

HA tag was immunoprecipitated from 0.2mg of 293 whole cells lysate transfected with C-terminal HA tagged gene with ARA782 at 1:10 dilution.
Ab ke-2:
GAR HRP untuk IP 1:500
Jalur 1: IP ARA782 dalam 293 lisat sel utuh ditransfeksi dengan gen bertanda C-terminal HA
Jalur 2: PBS sebagai pengganti ARA782 pada 293 lisat sel utuh ditransfeksi dengan gen bertanda C-terminal HA
Jalur 3: 293 lisat sel utuh ditransfeksi dengan gen bertanda C-terminal HA, 10 µg (input)
Paparan: 60an
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