HRP-conjugated β-Actin Rabbit mAb

Western blot analysis of various lysates using HRP-conjugated β-Actin Rabbit mAb  at 1:200000 dilution incubated overnight at 4℃.

Western blot analysis of various lysates using HRP-conjugated β-Actin Rabbit mAb at 1:200000 dilution incubated overnight at 4℃.

Catalog Number:MAB28000
Conjugate:HRP
Size:100 ug
Host:Rabbit
Isotype:IgG
Clone:D6A8
Immunogen:Recombinant protein (or fragment). This information is considered to be commercially sensitive.
Reactivity:Human,Mouse,Rat,Chicken,Zebrafish,Pig
Applications:WB 1:10000-1:50000-; ELISA Recommended starting concentration is 1 μg/mL. Please optimize the concentration based on your specific assay requirements.
Molecular Weight:42 kDa
Purification:Affinity purification
Form:Liquid
Synonyms:BRWS1; PS1TP5BP1

This gene encodes one of six different actin proteins. Actins are highly conserved proteins that are involved in cell motility, structure, integrity, and intercellular signaling. The encoded protein is a major constituent of the contractile apparatus and one of the two nonmuscle cytoskeletal actins that are ubiquitously expressed. Mutations in this gene cause Baraitser-Winter syndrome 1, which is characterized by intellectual disability with a distinctive facial appearance in human patients. Numerous pseudogenes of this gene have been identified throughout the human genome.

Applications

WB 1:10000-1:50000-; ELISA Recommended starting concentration is 1 μg/mL. Please optimize the concentration based on your specific assay requirements.

Immunogen

Recombinant protein (or fragment). This information is considered to be commercially sensitive.

Target Background

This gene encodes one of six different actin proteins. Actins are highly conserved proteins that are involved in cell motility, structure, integrity, and intercellular signaling. The encoded protein is a major constituent of the contractile apparatus and one of the two nonmuscle cytoskeletal actins that are ubiquitously expressed. Mutations in this gene cause Baraitser-Winter syndrome 1, which is characterized by intellectual disability with a distinctive facial appearance in human patients. Numerous pseudogenes of this gene have been identified throughout the human genome.

Synonyms:BRWS1; PS1TP5BP1

Storage

Store at -20℃. Avoid freeze / thaw cycles.

Buffer

PBS containing 50% glycerol and 0.05% BSA, preserved with proclin300 or sodium azide (as specified on the Certificate of Analysis), pH 7.3.

Western blot analysis of various lysates using HRP-conjugated β-Actin Rabbit mAb at 1:200000 dilution incubated overnight at 4℃.

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