Integrin beta 4/CD104 Antibody (M126) Summary
| Description |
Stable for at least 1 year at -20°C. |
| Immunogen |
Clone M126 was generated from a recombinant protein containing amino acid residues in the cytoplasmic region of human Integrin beta 4/CD104. This sequence is found in all three Integrin beta 4/CD104 isoforms and has 90% homology with rat and mouse Integrin beta 4/CD104. [UniProt# P16144] |
| Specificity |
This antibody detects a 200kDa protein corresponding to the molecular mass of Integrin beta 4/CD104 on SDS-PAGE immunoblots of human A431 cells. |
| Isotype |
IgG1 |
| Clonality |
Monoclonal |
| Host |
Mouse |
| Gene |
ITGB4 |
| Purity |
Protein A purified |
| Innovator's Reward |
Test in a species/application not listed above to receive a full credit towards a future purchase. |
Applications/Dilutions
| Dilutions |
- Immunocytochemistry/ Immunofluorescence 1:250
- Western Blot 1:1000
|
| Theoretical MW |
200 kDa. Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors. |
Packaging, Storage & Formulations
| Storage |
Store at -20C. |
| Buffer |
PBS, 1 mg/ml BSA and 50% glycerol |
| Preservative |
0.05% Sodium Azide |
| Purity |
Protein A purified |
Alternate Names for Integrin beta 4/CD104 Antibody (M126)
Background
Integrin beta 4 is a glycoprotein which associates with the a6 integrin to form the a6/b4 complex. Integrin alpha 6/beta 4 is a receptor for laminin. It plays a critical structural role in the hemidesmosome of epithelial cells. Defects in Integrin beta 4 gene are a cause of epidermolysis bullosa letalis with pyloric atresia (EB PA); also known as junctional epidermolysis bullosa with pyloric atresia (PA-JEB) or aplasia cutis congenita with gastrointestinal atresia. EB-PA is characterized by mucocutaneous fragility and gastrointestinal atresia, which most commonly affects the pylorus. Moreover, defects in Integrin beta 4 gene are a cause of generalized atrophic benign epidermolysis bullosa (GABEB). This nonlethal form of junctional epidermolysis bullosa is characterized by life long blistering of the skin, associated with hair and tooth abnormalities.
Limitations
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are
guaranteed for 1 year from date of receipt.
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