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Rabbit anti-ATP2A2 polyclonal antibody - C-terminal region

Catalog Number:OM112041
OM112041
Discount Price
OM112041-100ul
1~2 Week
100ul
OM112041-50ul
50ul
OM112041-20ul
20ul
1~2 Week
Product Profile
Product Name Rabbit anti-ATP2A2 polyclonal antibody - C-terminal region
Antibody Type Primary Antibodies
Antigen Alias ATP2B, DAR, DD, DKFZp686P0211, FLJ20293, FLJ38063, MGC45367, SERCA2
Immunogen The immunogen for anti-ATP2A2 antibody: synthetic peptide directed towards the C terminal of human ATP2A2
Key Feature
Clonality Polyclonal
Isotype IgG
Host Species Rabbit
Tested Applications WB
WB:1:500~1:2000
Notes:Optimal dilutions/concentrations should be determined by the researcher.
Species Reactivity BovineDogGuinea PigHorseMouseRatZebra Fish
Concentration 1mg/ml
Purification Affinity purified
Target Information
Gene Symbol ATP2A2
Gene Synonyms ATP2B
DAR
DD
DKFZp686P0211
FLJ20293
FLJ38063
MGC45367
SERCA2
Gene Full Name ATPase, Ca++ transporting, cardiac muscle, slow twitch 2
Gene Summary ATP2A2 is one of the SERCA Ca(2+)-ATPases, which are intracellular pumps located in the sarcoplasmic or endoplasmic reticula of muscle cells. This enzyme catalyzes the hydrolysis of ATP coupled with the translocation of calcium from the cytosol into the sarcoplasmic reticulum lumen, and is involved in regulation of the contraction/relaxation cycle. Mutations in this gene cause Darier-White disease, also known as keratosis follicularis, an autosomal dominant skin disorder characterized by loss of adhesion between epidermal cells and abnormal keratinization. Alternative splicing results in multiple transcript variants encoding different isoforms.This gene encodes one of the SERCA Ca(2+)-ATPases, which are intracellular pumps located in the sarcoplasmic or endoplasmic reticula of muscle cells. This enzyme catalyzes the hydrolysis of ATP coupled with the translocation of calcium from the cytosol to the sarcoplasmic reticulum lumen, and is involved in regulation of the contraction/relaxation cycle. Mutations in this gene cause Darier-White disease, also known as keratosis follicularis, an autosomal dominant skin disorder characterized by loss of adhesion between epidermal cells and abnormal keratinization. Alternative splicing results in two transcript variants encoding different isoforms.
Alternative Names ATP2B
DAR
DD
DKFZp686P0211
FLJ20293
FLJ38063
MGC45367
SERCA2
Molecular Weight(MW) 115kDa
Sequence 1042 amino acids
Database Links
Entrez Gene 488
SwissProt ID P16615
Protein Accession NP_733765
Application

Western blot

0.2-1 ug/mlELISA Titer: 1:62500Positive Control: MCF7 cell lysate
Application Notes WB:1:500~1:2000
Notes:Optimal dilutions/concentrations should be determined by the researcher.
Additional Information
Form Liquid
Storage Instructions Aliquot and store at -20°C. Avoid repeated freeze / thaw cycles
Storage Buffer phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
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