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Cusabio

SKU:CSB-PA823452LA01HU

TBC1D15 Antibody

TBC1D15 Antibody

Regular price $600.00 USD
Regular price Sale price $600.00 USD
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Size
Release Date 2022-04-01
Product Code CSB-PA823452LA01HU
Short Name TBC1D15 Antibody
Antibody Type Polyclonal Antibody
List Price $600/100ul
Species Reactivity Human, Mouse
Tested Applications ELISA, WB, IHC, IF
Dilution WB:1:500-1:2000,IHC:1:50-1:200,IF:1:100-1:300
Purification Method Antigen affinity purification
Buffer Formulation PBS, 0.02% Sodium Azide, 50% Glycerol, pH 7.3.
Antigen Recombinant human TBC1 domain family member 15 protein
Antigen Species Human
Uniprot ID Q8TC07
Target Name TBC1D15
Clonality Polyclonal
Host Species Rabbit
Isotype IgG
Conjugation Non-conjugated
Form Liquid
Storage Condition Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze.
TDS URL https://www.cusabio.com/datasheet/12555174/
Size 100ul

Image 1

Western Blot
Positive WB detected in: A549 whole cell lysate(30µg), HepG2 whole cell lysate(30µg), Hela whole cell lysate(30µg), 293T whole cell lysate(30µg), JK whole cell lysate(30µg), A431 whole cell lysate(30µg), SY5Y whole cell lysate(30µg),Mouse Brain tissue lysate(30µg),Mouse Liver tissue lysate(30µg)
All lanes: TBC1D15 antibody at 1:1000
Secondary
Goat polyclonal to rabbit IgG at 1/20000 dilution
Predicted band size: 80,78,79 kDa
Observed band size: 80 kDa
Exposure time: 30s

Image 2

IHC image of CSB-PA823452LA01HU diluted at 1:50 and staining in paraffin-embedded human kidney tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB. Secondary antibody only control: uses 1% BSA instead of primary antibody

Image 3

IHC image of CSB-PA823452LA01HU diluted at 1:50 and staining in paraffin-embedded humancolorectal cancer performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB. Secondary antibody only control: uses 1% BSA instead of primary antibody

Image 4

Immunofluorescence staining of Hela cell with CSB-PA823452LA01HU at 1:100, counter-stained with DAPI. The cells were fixed in 4% formaldehyde and and permeated by 0.2% TritonX-100 for 15 min. Then 10% normal goat serum to block non-specific protein-protein interactions . The cells were then incubated with the antibody overnight at 4℃. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L).

Image 5

Immunofluorescence staining of HepG2 cell with CSB-PA823452LA01HU at 1:100, counter-stained with DAPI. The cells were fixed in 4% formaldehyde and and permeated by 0.2% TritonX-100 for 15 min. Then 10% normal goat serum to block non-specific protein-protein interactions . The cells were then incubated with the antibody overnight at 4℃. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L).

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