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For research use only.

Verified Samples Verified Samples in WB: Hela, Mouse kidney, Mouse brain
Verified Samples in IHC: Human lung cancer
Verified Samples in IF: Human liver
Dilution WB 1:1000-2000,  IHC 1:100-1:300,  IF 1:50-1:200
Isotype IgG
Host Mouse
Reactivity Human,  Mouse,  Rat
Applications WB,  IHC-p,  IF
Clonality Monoclonal
Immunogen Synthetic Peptide
Abbre CK7
Synonyms 55K type II cytoskeletal,  CK 7,  CK-7,  CK7,  Cytokeratin 7,  Cytokeratin-7,  D15Wsu77e,  K2C7,  K7,  Kerat,  Keratin,  Keratin 7,  Keratin type II cytoskeletal 7,  simple epithelial,  simple epithelial type I,  type II,  type II cytoskeletal 7
Swissprot
Calculated MW 51 kDa
Observed MW 54 kDa
The actual band is not consistent with the expectation.

Western blotting is a method for detecting a certain protein in a complex sample based on the specific binding of antigen and antibody. Different proteins can be divided into bands based on different mobility rates. The mobility is affected by many factors, which may cause the observed band size to be inconsistent with the expected size. The common factors include:

1. Post-translational modifications: For example, modifications such as glycosylation, phosphorylation, methylation, and acetylation will increase the molecular weight of the protein.

2. Splicing variants: Different expression patterns of various mRNA splicing bodies may produce proteins of different sizes.

3. Post-translational cleavage: Many proteins are first synthesized into precursor proteins and then cleaved to form active forms, such as COL1A1.

4. Relative charge: the composition of amino acids (the proportion of charged amino acids and uncharged amino acids).

5. Formation of multimers: For example, in protein dimer, strong interactions between proteins can cause the bands to be larger. However, the use of reducing conditions can usually avoid the formation of multimers.

If a protein in a sample has different modified forms at the same time, multiple bands may be detected on the membrane.

Cellular Localization Cytoplasm
Tissue Specificity Expressed in cultured epidermal, bronchial and mesothelial cells but absent in colon, ectocervix and liver. Observed throughout the glandular cells in the junction between stomach and esophagus but is absent in the esophagus.
Concentration 1 mg/mL
Buffer Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer, 0.5% protein protectant and 50% glycerol.
Purification Method Protein A purification
Research Areas Cancer,  Signal Transduction
Clone No. 2B5
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.
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).
Other Clones

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Unconjugated

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