Anti-ADGRE5 antibody [HL1925] - BSA and Azide free
- Recombinant
- KO Validated
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Rabbit Recombinant Monoclonal CD97 antibody. Carrier free. Suitable for WB, IP and reacts with Human, Transfected cell lysate - Human samples. Immunogen corresponding to Recombinant Fragment Protein within Human ADGRE5.
View Alternative Names
CD97, ADGRE5, Adhesion G protein-coupled receptor E5, Leukocyte antigen CD97
- IP
Supplier Data
Immunoprecipitation - Anti-ADGRE5 antibody [HL1925] - BSA and Azide free (AB325846)
Immunoprecipitation of CD97 protein from U937 using 5 μg of ab325846. Western blot analysis was performed using ab325846. Secondary : HRP-conjugated anti rabbit IgG antibody.
All lanes:
Immunoprecipitation - Anti-ADGRE5 antibody [HL1925] - BSA and Azide free (ab325846) at 5 µg
Lane 1:
Input
Lane 3:
Immunoprecipitation of CD97 protein from U937
Secondary
All lanes:
HRP-conjugated anti rabbit IgG antibody
false
- WB
Supplier Data
Western blot - Anti-ADGRE5 antibody [HL1925] - BSA and Azide free (AB325846)
Wild-type (WT) and ADGRE5 knockout (KO) HeLa cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with ab325846 diluted at 1 : 500. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.
All lanes:
Western blot - Anti-ADGRE5 antibody [HL1925] - BSA and Azide free (ab325846) at 1/500 dilution
Lane 1:
Wild-type (WT) HeLa cell extracts at 30 µg
Lane 2:
ADGRE5 knockout (KO) HeLa cell extracts at 30 µg
Secondary
All lanes:
HRP-conjugated anti-rabbit IgG antibody
false
- WB
Supplier Data
Western blot - Anti-ADGRE5 antibody [HL1925] - BSA and Azide free (AB325846)
Various whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with ab325846 diluted at 1 : 500. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody. Corresponding RNA expression data for the same cell lines are based on Human Protein Atlas program.
All lanes:
Western blot - Anti-ADGRE5 antibody [HL1925] - BSA and Azide free (ab325846) at 1/500 dilution
Lane 1:
293T whole cell extracts at 30 µg
Lane 2:
A431 whole cell extracts at 30 µg
Secondary
All lanes:
HRP-conjugated anti-rabbit IgG antibody
false
- WB
Supplier Data
Western blot - Anti-ADGRE5 antibody [HL1925] - BSA and Azide free (AB325846)
U937 whole cell and membrane extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membranes were blotted with ab325846 diluted at 1 : 1000 and competitor's antibody diluted at 1 : 1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.
All lanes:
Western blot - Anti-ADGRE5 antibody [HL1925] - BSA and Azide free (ab325846) at 1/1000 dilution
Lane 1:
U937 whole cell extracts at 30 µg
Lane 2:
U937 membrane extracts at 30 µg
Secondary
All lanes:
HRP-conjugated anti-rabbit IgG antibody
true
- WB
Supplier Data
Western blot - Anti-ADGRE5 antibody [HL1925] - BSA and Azide free (AB325846)
Wild-type (WT) and CD97 knockout (KO) HeLa cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membranes were blotted with ab325846 diluted at 1 : 1000 and the highly cited competitor's antibody diluted at 1 : 1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.
All lanes:
Western blot - Anti-ADGRE5 antibody [HL1925] - BSA and Azide free (ab325846) at 1/1000 dilution
Lane 1:
Boiled Wild-type (WT) HeLa cell extracts at 30 µg
Lane 2:
Boiled CD97 knockout (KO) HeLa cell extracts at 30 µg
Lane 3:
Unboiled Wild-type (WT) HeLa cell extracts at 30 µg
Lane 4:
Unboiled CD97 knockout (KO) HeLa cell extracts at 30 µg
Secondary
All lanes:
HRP-conjugated anti-rabbit IgG antibody
true
- WB
Supplier Data
Western blot - Anti-ADGRE5 antibody [HL1925] - BSA and Azide free (AB325846)
Untreated (–) and treated (+) U937 whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with ab325846 diluted at 1 : 2000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.
All lanes:
Western blot - Anti-ADGRE5 antibody [HL1925] - BSA and Azide free (ab325846) at 1/2000 dilution
Lane 1:
Untreated (–) U937 whole cell extracts at 30 µg
Lane 2:
24 ug/mL Tunicamycin, 24hr treated (+) U937 whole cell extracts at 30 µg
Secondary
All lanes:
HRP-conjugated anti-rabbit IgG antibody
true
- WB
Supplier Data
Western blot - Anti-ADGRE5 antibody [HL1925] - BSA and Azide free (AB325846)
Boiled and unboiled U937 whole cell and membrane extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with ab325846 diluted at 1 : 2000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody, and the signal was developed with Trident femto Western HRP Substrate.
All lanes:
Western blot - Anti-ADGRE5 antibody [HL1925] - BSA and Azide free (ab325846) at 1/2000 dilution
Lane 1:
Boiled U937 whole cell extracts at 30 µg
Lane 2:
Boiled U937 membrane extracts at 30 µg
Lane 3:
Unboiled U937 whole cell extracts at 30 µg
Lane 4:
Unboiled U937 membrane extracts at 30 µg
Secondary
All lanes:
HRP-conjugated anti-rabbit IgG antibody
true
- WB
Supplier Data
Western blot - Anti-ADGRE5 antibody [HL1925] - BSA and Azide free (AB325846)
Non-transfected (–) and transfected (+) 293T whole cell extracts (30 ug) were separated by 7.5% SDS-PAGE, and the membrane was blotted with ab325846 diluted at 1 : 2000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.
All lanes:
Western blot - Anti-ADGRE5 antibody [HL1925] - BSA and Azide free (ab325846) at 1/2000 dilution
Lane 1:
Non-transfected (–) 293T whole cell extracts at 30 µg
Lane 2:
DDDDK-tagged ADGRE5 transfected (+) 293T whole cell extracts at 30 µg
Secondary
All lanes:
HRP-conjugated anti-rabbit IgG antibody
false
Reactivity data
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