Cytokeratin 7 Rabbit Monoclonal Antibody(ARA806)

Key features and details

  • Target: Cytokeratin 7
  • Source/Host: Rabbit
  • Reactivity: Human
  • Clonality: Monoclonal
  • Applications: WB,IHC,IF/ICC,FC,IP
  • Conjugation: Unconjugated
  • Storage: at-20°C
  • Brand:
CAT.NO. : ARA6593
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Size:
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Product Details
Background
Blocks interferon-dependent interphase and stimulates DNA synthesis in cells. Involved in the translational regulation of the human papillomavirus type 16 E7 mRNA (HPV16 E7).
Application
To ensure optimal assay performance, AREX recommends conducting reagent titration tailored to each testing system for optimal detection results.

WB

1:2000-1:5000

IHC

1:1600-1:3200

IF/ICC

1:800-1:2000

FC

1:200-1:800

IP

1:50

*Results are sample-specific. Please refer to your local assay conditions and test parameters for reference.
Overview

Description

Rabbit Monoclonal Antibody to Cytokeratin 7

Antibody Type

Primary antibody

Predicted MW

51kDa

Immunogen

A synthetic peptide corresponding to residues aa1- 100 of Cytokeratin 7 was used as an immunogen.

Purification

ProA affinity purified IgG

Form/Buffer

PBS 59%, Sodium azide 0.01%, Glycerol 40%, BSA 0.81%.

Alternative Names

SCL; Keratin, type II cytoskeletal 7; Cytokeratin-7; CK-7; Keratin-7; K7; Sarcolectin; Type-II keratin Kb7

Gene Symbol

KRT7

Entrez Gene

3855(Human)

Swissprot

P08729

*AREX continuously optimizes our products. Webpage content may not reflect the latest updates. For inquiries, please contact info@arexbio.com or your local distributor.
*Clone Number, Reactivity, Source/Host and Clonality can be found in the product name and Key Features section above.
Data

All lanes: Anti-Cytokeratin 7 antibody at 1:10,000 dilution
Predicted MW: 51 kDa
Observed MW: 51 kDa

Lane 1: Hela
Lane 2: A549
Lane 3: HaCat

Lysates at 10 µg per lane
2nd Ab:
GAR HRP(H+L) 1:5,000
Exposure: 60s

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human thyroid cancer tissue labelling Cytokeratin 7 with ARA806 at 1:3,200. Heat mediated antigen retrieval was performed using Tris/EDTA buffer pH 9.0.

ARA806 staining Cytokeratin 7 in Hela cells 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<sup>®</sup> 488-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<sup>®</sup> 488-conjugated Goat Anti-Rabbit IgG (1:500).

Overlay histogram showing Hela cells stained with ARA806 (Red). The cells were fixed with 4% paraformaldehyde (10 min) and then permeabilized with 0.1% TritonX-100 for 15 min. The cells were then incubated in the antibody (ARA806, 1:800 dilution) in 1x PBS/1% BSA for 30 min at room temperature. The secondary antibody used was a Goat Anti-Rabbit Alexa Fluor<sup>®</sup> 488 (IgG H+L) at 1:2,000 dilution for 20 min at room temperature. Unlabelled sample (Black) was used as a control.

Cytokeratin 7 was immunoprecipitated from 0.4mg of Hela whole cell lysate with ARA806 at 1:50 dilution.
2nd Ab:
GAR HRP for IP 1:500

Lane 1: ARA806 IP in Hela whole cell lysate
Lane 2: PBS instead of ARA806 in Hela whole cell lysate
Lane 3: Hela whole cell lysate, 10 µg (input)
Exposure: 50s

Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Note
For Research Use Only. Not for diagnostic, therapeutics, prophylactic or in vivo use.
FAQs
What are the main types of research antibodies and how do they differ?
Research antibodies are mainly divided into monoclonal antibodies and polyclonal antibodies. Monoclonal antibodies typically offer higher specificity and better batch-to-batch consistency, while polyclonal antibodies often provide stronger affinity but may show more variation between batches. The choice depends on your specific experimental needs.
How can I tell if a research antibody is suitable for my experiment?
It is recommended to carefully review the product datasheet for validated applications, species reactivity, recommended dilutions, and published references. For new antibodies, performing a small-scale validation with positive control samples is usually helpful.
Can improper storage of research antibodies affect experimental results?
Yes. Antibodies are sensitive to temperature, repeated freeze-thaw cycles, and contamination. Improper storage may lead to reduced activity, increased background, or weaker signals. It is best to follow the storage instructions provided in the product datasheet.
Why doesn’t the recommended dilution in the datasheet work well in my experiment?
The recommended dilution is based on the supplier’s test conditions. Factors such as sample type, fixation method, and detection system in your lab can influence the optimal working concentration. Performing a dilution series optimization in your own system is often necessary.
What precautions should I take when using a newly purchased research antibody for the first time?
It is advisable to briefly centrifuge the antibody (especially concentrated or lyophilized ones), then perform a small-scale pilot experiment using the recommended conditions. Recording the batch number and usage date is also helpful for future tracking.
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