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Read our guarantee »Products:Signal Transduction >> Cytoskeleton / ECM >> Cell Adhesion >> Integrins >> Beta
Anti-Integrin beta 4 antibody [M126]
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Mouse monoclonal [M126] to Integrin beta 4
ab29042 recognises all three isoforms of integrin beta 4 Beta 4A, beta 4B and beta 4C.
ELISA, WB, ICC, ICC/IFmore details
Reacts with
Mouse, Rat, Dog, Human
recombinant protein containing amino acid residues in the cytoplasmic region of human integrin beta 4.
A431 cell lysate.
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
Preservative: 0.05% Sodium Azide
Constituents: 50% Glycerol, PBS, 1mg/ml BSA
Concentration information loading...
Protein A purified
Monoclonal
M126
IgG1
Signal Transduction >> Cytoskeleton / ECM >> Cell Adhesion >> Integrins >> Beta
Western blot - Integrin beta 4 antibody [M126] (ab29042)
(enlarge)
Our Abpromise guarantee covers the use of ab29042 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
ELISA: 1/2000
WB: 1/1000Predicted molecular weight: 202 kDa.(In 5% non fat milk, PBS, 0.04% Tween 20 for 1 hour at room temperature. )
ICC: 1/250
ICC/IF: Use at an assay dependent concentration. (PubMed: 21042878)
Integrin alpha-6/beta-4 is a receptor for laminin. It plays a critical structural role in the hemidesmosome of epithelial cells.
Integrin alpha-6/beta-4 is predominantly expressed by epithelia. Isoform beta-4D is also expressed in colon and placenta. Isoform beta-4E is also expressed in epidermis, lung, duodenum, heart, spleen and stomach.
Defects in ITGB4 are a cause of epidermolysis bullosa letalis with pyloric atresia (EB-PA) [MIM:226730]; also known as junctional epidermolysis bullosa with pyloric atresia (PA-JEB) or aplasia cutis congenita with gastrointestinal atresia. EB-PA is an autosomal recessive, frequently lethal, epidermolysis bullosa with variable involvement of skin, nails, mucosa, and with variable effects on the digestive system. It is characterized by mucocutaneous fragility, aplasia cutis congenita, and gastrointestinal atresia, which most commonly affects the pylorus. Pyloric atresia is a primary manifestation rather than a scarring process secondary to epidermolysis bullosa.
Defects in ITGB4 are a cause of generalized atrophic benign epidermolysis bullosa (GABEB) [MIM:226650]. GABEB is a non-lethal, adult form of junctional epidermolysis bullosa characterized by life-long blistering of the skin, associated with hair and tooth abnormalities.
Belongs to the integrin beta chain family.
Contains 1 Calx-beta domain.
Contains 4 fibronectin type-III domains.
Contains 1 PSI domain.
Contains 1 VWFA domain.
The fibronectin type-III-like domains bind BPAG1 and plectin and probably also recruit BP230.
Membrane.
Target information above from: UniProt accessionP16144
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Western blot - Integrin beta 4 antibody [M126] (ab29042)
![Western blot - Integrin beta 4 antibody [M126] (ab29042)](/ps/datasheet/Images/29/ab29042/ab29042_1.jpg)
All lanes : Anti-Integrin beta 4 antibody [M126] (ab29042)
Lane 1 : A431 (25 µg/lane) serum starved overnight
Lane 2 : A431 (25 µg/lane) serum treated with pervanadate (1 mM) for 30 min
Predicted band size : 202 kDa
This product has been referenced in:
See all 3 publications for this product
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