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Mouse Monoclonal Integrin alpha6 antibody (STJ98511)
Supplier: St John’s Laboratory Ltd.
Recommended applications: WB, IF
Recommended dilution: WB 1:1000-1:2000; IF 1:100-1:500
Recommended protocols: check protocols
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Check alternative names for the antibodyExpand
ITGA6 antibody,|Alpha6p antibody|CD49 antigen-like family member F antibody|CD49f antibody|Integrin alpha6B antibody|Integrin, alpha 6 antibody|ITA6_HUMAN antibody|ITGA6 antibody|ITGA6B antibody|Processed integrin alpha-6 antibody|VLA 6 antibody|VLA-6 antibody|Anti-Integrin alpha 6 antibody [MP 4F10] (ab20142)
SCBT cat No: sc-71426|sc-71427|sc-71423|sc-59842|sc-53356|sc-47772|sc-13542|sc-6596|sc-374057|sc-19622|sc-10730|sc-6597|sc-80554|sc-81807|sc-27710|
Integrin alpha6 Monoclonal Antibody
|Catalogue No.|| |
Human, Mouse, Rat, Cow, Dog, Pig
Integrin alpha6 Monoclonal Antibody detects endogenous levels of Integrin alpha6 protein.
Purified recombinant human Integrin alpha6 (N-terminus) protein fragments expressed in Ecoli
|Recommended dilution|| |
WB 1:1000-1:2000; IF 1:100-1:500
Integrin alpha6 Antibody was tube-contained. Purified in buffer containing 0.1M Tris-Glycine (pH 7.4, 150 mM NaCl) with 0.2% sodium azide, 50% glycerol.
Integrin alpha6 Antibody was purified using affinity purification.
-20 Celsius degree. Avoid repeated freeze/thaw cycles.
|Alternative antibody names|| |
Integrin alpha-6 antibody, CD49 antigen-like family member F antibody, VLA-6 antibody, CD antigen CD49f antibody
|Protein names|| |
Integrin alpha-6 , CD49 antigen-like family member F , VLA-6 , CD antigen CD49f
|Involvement in disease|| |
Epidermolysis bullosa letalis, with pyloric atresia (EB-PA) [MIM:226730]: 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. Note: The disease is caused by mutations affecting the gene represented in this entry.
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St John’s Laboratory Ltd.
|Product type|| |
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