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Rabbit Polyclonal Cleaved-Integrin alpha6 LC (E942) antibody (STJ90089)
Supplier: St John’s Laboratory Ltd.
Recommended applications: WB, ELISA
Recommended dilution: WB 1:500-1:2000; ELISA 1:10000;
Recommended protocols: check protocols
Click or hover above images to see image description for Cleaved-Integrin alpha6 LC (E942) Polyclonal Antibody.
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|
Cleaved-Integrin alpha6 LC (E942) Polyclonal Antibody
|Catalogue No.|| |
Cleaved-Integrin alpha6 LC (E942) Polyclonal Antibody detects endogenous levels of fragment of activated Integrin alpha6 LC protein resulting from cleavage adjacent to E942.
Synthesized peptide derived from Cleaved-Integrin alpha6 LC (E942) at AA range 900-980
|Recommended dilution|| |
WB 1:500-1:2000; ELISA 1:10000;
|Molecular weight|| |
Cleaved-Integrin alpha6 LC (E942) Antibody was tube-contained. Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Cleaved-Integrin alpha6 LC (E942) Antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
-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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