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Rabbit anti-GNAS polyclonal antibody - C-terminal region

Catalog Number:OM110575
OM110575
Discount Price
OM110575-100ul
1~2 Week
100ul
OM110575-50ul
50ul
OM110575-20ul
20ul
1~2 Week
Product Profile
Product Name Rabbit anti-GNAS polyclonal antibody - C-terminal region
Antibody Type Primary Antibodies
Antigen Alias AHO, C20orf45, GNAS1, GNASXL, GPSA, GSA, GSP, NESP, NESP55, PHP1A, PHP1B, POH, XL2, XLalphas, PHP1C
Immunogen The immunogen for anti-GNAS antibody: synthetic peptide directed towards the C terminal of human GNAS
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 PigHorseHumanMousePigRatZebra Fish
Concentration 1mg/ml
Purification Protein A
Target Information
Gene Symbol GNAS
Gene Synonyms AHO
C20orf45
GNAS1
GNASXL
GPSA
GSA
GSP
NESP
NESP55
PHP1A
PHP1B
POH
XL2
XLalphas
PHP1C
Gene Full Name GNAS complex locus
Gene Summary This locus has a highly complex imprinted expression pattern. It gives rise to maternally, paternally, and biallelically expressed transcripts that are derived from four alternative promoters and 5' exons. Mutations in this gene result in pseudohypoparathyroidism type 1a, pseudohypoparathyroidism type 1b, Albright hereditary osteodystrophy, pseudopseudohypoparathyroidism, McCune-Albright syndrome, progressive osseus heteroplasia, polyostotic fibrous dysplasia of bone, and some pituitary tumors.This gene has a highly complex imprinted expression pattern. It encodes maternally, paternally, and biallelically expressed proteins which are derived from alternatively spliced transcripts with alternate 5' exons. Each of the upstream exons is within a differentially methylated region, commonly found in imprinted genes. However, the close proximity (14 kb) of two oppositely expressed promoter regions is unusual. In addition, one of the alternate 5' exons introduces a frameshift relative to the other transcripts, resulting in one isoform which is structurally unrelated to the others. An antisense transcript exists, and may regulate imprinting in this region. Mutations in this gene result in pseudohypoparathyroidism type 1a (PHP1a), which has an atypical autosomal dominant inheritance pattern requiring maternal transmission for full penetrance. There are RefSeqs representing four transcript variants of this gene. Other transcript variants including four additional exons have been described; however, their full length sequences have not been determined.
Alternative Names AHO
C20orf45
GNAS1
GNASXL
GPSA
GSA
GSP
NESP
NESP55
PHP1A
PHP1B
POH
XL2
XLalphas
PHP1C
Molecular Weight(MW) 42kDa
Sequence 380 amino acids
Database Links
Entrez Gene 2778
SwissProt ID Q5FWY2
Protein Accession NP_536351
Application

Western blot

2.5ug/mlPositive Control: Jurkat 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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