重组Anti-Cathepsin L/V/K/H抗体[EPR8011]
Anti-Cathepsin L/V/K/H antibody [EPR8011]
- 20ul selling size
- RabMAb
- Recombinant
- 了解详情
5
(6 Reviews)
|
(20 Publications)
Rabbit Recombinant Monoclonal Cathepsin L/MEP antibody. Suitable for IHC-P, ELISA, WB, ICC/IF, Flow Cyt (Intra) and reacts with Human, Mouse, Rat samples. Cited in 20 publications.
查看别名
CTSL1, CTSL, Procathepsin L, Cathepsin L1, Major excreted protein, MEP, CPSB, CTSH, Pro-cathepsin H, CTSO, CTSO2, CTSK, Cathepsin K, Cathepsin O, Cathepsin O2, Cathepsin X, CATL2, CTSL2, CTSU, UNQ268/PRO305, CTSV, Cathepsin L2, Cathepsin U, Cathepsin V
- ICC/IF
AbReview36173****
Immunocytochemistry/ Immunofluorescence - Anti-Cathepsin L/V/K/H antibody [EPR8011] (AB133641)
Unpurified ab133641 staining Cathepsin L in Human HepaRG cell by ICC/IF (Immunocytochemistry/immunofluorescence). Cells were fixed with formaldehyde, permeabilized with 0.1% Triton X-100 and blocked with 1% milk for 30 minutes at room temperature. Samples were incubated with primary antibody (1/1000) for 30 minutes. An Alexa Fluor® 488-conjugated Donkey anti-rabbit IgG polyclonal (1/400) was used as the secondary antibody.
This image is courtesy of an Abreview submitted by Alina Macovei
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-Cathepsin L/V/K/H antibody [EPR8011] (AB133641)
Immunocytochemistry/Immunofluorescence analysis of HT-29 cells labelling Cathepsin L with purified ab133641 at 1/100. Cells were fixed with 100% methanol and permeabilized with 0.1% Triton X-100. ab150077 an Alexa Fluor® 488-conjugated goat anti-rabbit IgG (1/500) was used as the secondary antibody. DAPI (blue) was used as the nuclear counterstain. ab7291 a mouse anti-tubulin (1/500) and ab150120 an Alexa Fluor® 594-conjugated goat anti-mouse IgG (1/500) were also used.
Control 1 : primary antibody (1/100) and secondary antibody ab150120 an Alexa Fluor® 594-conjugated goat anti-mouse IgG (1/500).
Control 2 : ab7291 (1/1000) and secondary antibody ab150077 an Alexa Fluor® 488-conjugated goat anti-rabbit IgG (1/500).
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Cathepsin L/V/K/H antibody [EPR8011] (AB133641)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human kidney tissue labelling Cathepsin L with unpurified ab133641 at a 1/50 dilution.
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Cathepsin L/V/K/H antibody [EPR8011] (AB133641)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human kidney tissue labelling Cathepsin L with purified ab133641 at 1/100. Heat mediated antigen retrieval was performed using Tris/EDTA buffer pH 9. ab97051 a HRP-conjugated goat anti-rabbit IgG (H+L) was used as the secondary antibody (1/500). Negative control using PBS instead of primary antibody. Counterstained with hematoxylin.
- Flow Cyt (Intra)
Lab
Flow Cytometry (Intracellular) - Anti-Cathepsin L/V/K/H antibody [EPR8011] (AB133641)
ab133641 staining Cathepsin Lin the human cell line HepG2 (human hepatocellular carcinoma) by intracellular flow cytometry. Cells were fixed with 4% paraformaldehyde and the sample was incubated with the primary antibody at a dilution of 1/20. A goat anti rabbit IgG (Alexa Fluor® 488) at a dilution of 1/2000 was used as the secondary antibody.
Isoytype control : Rabbit monoclonal IgG (Black)
Unlabelled control : Cell without incubation with primary antibody and secondary antibody (Blue)
- ELISA
Supplier Data
ELISA - Anti-Cathepsin L/V/K/H antibody [EPR8011] (AB133641)
Antigen : CATL_HUMAN CATV_HUMAN CATS_HUMAN CATK_HUMAN CATH_HUMAN
Antigen concentration : 1000ng/ml
Primary antibody concentration range : 0~1000ng/ml
Secondary antibody : Alkaline Phosphatase-conjugated AffiniPure Goat Anti-Rabbit IgG(H+L)
Secondary antibody concentration : 1/2500
- WB
Unknown
Western blot - Anti-Cathepsin L/V/K/H antibody [EPR8011] (AB133641)
Blocking and dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-Cathepsin L/V/K/H antibody [EPR8011] (ab133641) at 1/20000 dilution
All lanes:
HepG2 cell lysate at 20 µg
Secondary
All lanes:
Peroxidase conjugated goat anti-rabbit IgG (H+L) at 1/1000 dilution
Predicted band size: 38 kDa
Observed band size: 38 kDa
false
- WB
Unknown
Western blot - Anti-Cathepsin L/V/K/H antibody [EPR8011] (AB133641)
All lanes:
Western blot - Anti-Cathepsin L/V/K/H antibody [EPR8011] (ab133641) at 1/1000 dilution
Lane 1:
A549 cell lysate at 10 µg
Lane 2:
HCT-116 cell lysate at 10 µg
Lane 3:
NIH/3T3 cell lysate at 10 µg
Lane 4:
PC-12 cell lysate at 10 µg
Secondary
All lanes:
HRP-conjugated goat anti-rabbit IgG at 1/2000 dilution
Predicted band size: 38 kDa
false
- WB
Unknown
Western blot - Anti-Cathepsin L/V/K/H antibody [EPR8011] (AB133641)
Blocking and dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-Cathepsin L/V/K/H antibody [EPR8011] (ab133641) at 1/10000 dilution
Lane 1:
HCT-116 cell lysate at 10 µg
Lane 2:
A549 cell lysate at 10 µg
Secondary
All lanes:
Peroxidase conjugated goat anti-rabbit IgG (H+L) at 1/1000 dilution
Predicted band size: 38 kDa
Observed band size: 38 kDa
false
- WB
Unknown
Western blot - Anti-Cathepsin L/V/K/H antibody [EPR8011] (AB133641)
All lanes:
Western blot - Anti-Cathepsin L/V/K/H antibody [EPR8011] (ab133641) at 1/1000 dilution
All lanes:
HepG2 cell lysate at 10 µg
Secondary
All lanes:
HRP-conjugated goat anti-rabbit IgG at 1/2000 dilution
Predicted band size: 38 kDa
false
- WB
Unknown
Western blot - Anti-Cathepsin L/V/K/H antibody [EPR8011] (AB133641)
Blocking and dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-Cathepsin L/V/K/H antibody [EPR8011] (ab133641) at 1/20000 dilution
Lane 1:
NIH/3T3 cell lysate at 20 µg
Lane 2:
PC-12 cell lysate at 20 µg
Secondary
All lanes:
Peroxidase conjugated goat anti-rabbit IgG (H+L) at 1/1000 dilution
Predicted band size: 38 kDa
Observed band size: 38 kDa
false
- ELISA
Supplier Data
ELISA - Anti-Cathepsin L/V/K/H antibody [EPR8011] (AB133641)
Direct ELISA antigen dose-response curve using purified ab133641.Antigen concentration of 1000ng/mL.Alkaline Phosphatase conjugated AffiniPure goat anti-rabbit IgG(H+L)(1/2500) was used as the secondary antibody.
- WB
Supplier Data
Western blot - Anti-Cathepsin L/V/K/H antibody [EPR8011] (AB133641)
Blocking buffer and concentration : 5% NFDM/TBST
Diluting buffer and concentration : 5% NFDM/TBST
Observed MW : 30
Exposure time : 3 minutes
Lane 1:
Western blot - Anti-Cathepsin L + V antibody [33/2] (<a href='/products/primary-antibodies/cathepsin-l-v-antibody-33-2-ab6314'>ab6314</a>) at 1/20 dilution
Lane 1:
Western blot - Anti-Cathepsin L/V/K/H antibody [EPR8011] (ab133641) at 1/20 dilution
Lane 2:
Western blot - Anti-Cathepsin L/V/K/H antibody [EPR8011] (ab133641) at 1/100 dilution
Lane 2:
Western blot - Anti-Cathepsin L + V antibody [33/2] (<a href='/products/primary-antibodies/cathepsin-l-v-antibody-33-2-ab6314'>ab6314</a>) at 1/100 dilution
Lane 3:
Anti-His tag at 1/10000 dilution
All lanes:
Human Cathepsin L recombinant protein fraction
Secondary
Lanes 1 and 3:
Peroxidase conjugated Goat Anti-Rabbit IgG, (H+L) at 1/1000 dilution
Lane 2:
Rabbit anti-Mouse IgG at 1/2000 dilution
Predicted band size: 38 kDa
false
- WB
Supplier Data
Western blot - Anti-Cathepsin L/V/K/H antibody [EPR8011] (AB133641)
Blocking buffer and concentration : 5% NFDM/TBST
Diluting buffer and concentration : 5% NFDM/TBST
Observed MW : 30
Exposure time : 3 minutes
Lane 1:
Western blot - Anti-Cathepsin L/V/K/H antibody [EPR8011] (ab133641) at 1/20 dilution
Lane 1:
Western blot - Anti-Cathepsin L + V antibody [33/2] (<a href='/products/primary-antibodies/cathepsin-l-v-antibody-33-2-ab6314'>ab6314</a>) at 1/20 dilution
Lanes 2 and 4:
Western blot - Anti-Cathepsin L + V antibody [33/2] (<a href='/products/primary-antibodies/cathepsin-l-v-antibody-33-2-ab6314'>ab6314</a>) at 1/100 dilution
Lanes 2 and 4:
Western blot - Anti-Cathepsin L/V/K/H antibody [EPR8011] (ab133641) at 1/100 dilution
Lane 3:
Western blot - Anti-Cathepsin L/V/K/H antibody [EPR8011] (ab133641) at 1/500 dilution
Lane 3:
Western blot - Anti-Cathepsin L + V antibody [33/2] (<a href='/products/primary-antibodies/cathepsin-l-v-antibody-33-2-ab6314'>ab6314</a>) at 1/500 dilution
Lane 5:
Western blot - Anti-Cathepsin L/V/K/H antibody [EPR8011] (ab133641) at 1/1000 dilution
Lane 5:
Western blot - Anti-Cathepsin L + V antibody [33/2] (<a href='/products/primary-antibodies/cathepsin-l-v-antibody-33-2-ab6314'>ab6314</a>) at 1/1000 dilution
Lane 6:
Anti-His tag at 1/10000 dilution
All lanes:
Human Cathepsin V recombinant protein fraction
Secondary
Lanes 1 - 3:
Peroxidase conjugated Goat Anti-Rabbit IgG, (H+L) at 1/1000 dilution
Lanes 4 - 5:
Rabbit Anti-Mouse secondary ab at 1/2000 dilution
Lane 6:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 38 kDa
false
- OI-RD Scanning
Unknown
OI-RD Scanning - Anti-Cathepsin L/V/K/H antibody [EPR8011] (AB133641)
We have systematically measured KD (the equilibrium dissociation constant between the antibody and its antigen), of more than 840 recombinant antibodies to assess not only their individual KD values but also to see the average affinity of antibody. Based on the comparison with published literature values for mouse monoclonal antibodies, Recombinant antibodies appear to be on average 1-2 order of magnitude higher affinity.
不同偶联物与剂型 (10)
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Anti-Cathepsin L/V/K/H antibody [EPR8011] - BSA and Azide free
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660 APC
APC Anti-Cathepsin L/V/K/H antibody [EPR8011]
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519 Alexa Fluor® 488
Alexa Fluor® 488 Anti-Cathepsin L/V/K/H antibody [EPR8011]
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565 Alexa Fluor® 555
Alexa Fluor® 555 Anti-Cathepsin L/V/K/H antibody [EPR8011]
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603 Alexa Fluor® 568
Alexa Fluor® 568 Anti-Cathepsin L/V/K/H antibody [EPR8011]
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617 Alexa Fluor® 594
Alexa Fluor® 594 Anti-Cathepsin L/V/K/H antibody [EPR8011]
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665 Alexa Fluor® 647
Alexa Fluor® 647 Anti-Cathepsin L/V/K/H antibody [EPR8011]
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775 Alexa Fluor® 750
Alexa Fluor® 750 Anti-Cathepsin L/V/K/H antibody [EPR8011]
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HRP Anti-Cathepsin L/V/K/H antibody [EPR8011]
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578 PE
PE Anti-Cathepsin L/V/K/H antibody [EPR8011]
反应性数据
产品详情
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
性能和储存信息
形式
纯化工艺
存储溶液
运输条件
推荐的短期储存时间
推荐的短期储存条件
推荐的长期储存条件
分装信息
储存信息
补充信息
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Cathepsins regulate cellular homeostasis and modulate various physiological processes. These proteases perform their functions within the lysosomal compartment although they can also participate in extracellular matrix remodeling and other non-lysosomal roles. Cathepsin K for example is part of the cathepsin protein family and aids in degrading collagen therefore playing a pivotal role in bone turnover and resorption. Cathepsins can act independently or in some cases are part of larger enzyme complexes enhancing their proteolytic activity to handle different substrates driven by the physiological demand.
Pathways
Cathepsins key in the lysosomal degradation pathway and influence other signaling cascades like the apoptotic pathway. The regulation of these pathways often involves interactions with other proteins such as pro-apoptotic members of the Bcl-2 family facilitating cell death under certain conditions. Cathepsin L contributes to the antigen processing pathway linking it to the immune response. Cathepsin K on the other hand acts closely with structural proteins like collagen in the bone metabolism pathway highlighting its significance in skeletal development and maintenance.
产品实验方案
- Visit the General protocols
- Visit the Troubleshooting
靶点信息
其他靶点
文献 (20)
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