Sox-9 (phospho Ser181) rabbit pAb

Sox-9 (phospho Ser181) rabbit pAb

AO-06-ES7254-50

Sox-9 (phospho Ser181) rabbit pAb 50μL

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Antibody Product Overview

ELK.NoES7254
Product nameSox-9 (phospho Ser181) rabbit pAb
ReactivityHuman;Mouse
ApplicationsWB;IHC;IF;ELISA
Other nameSOX9; Transcription factor SOX-9
Size50μL
Unit price ($)148
Human gene ID6662
Human Swiss-ProtP48436
SourceRabbit
IsotypeIgG
TargetSox-9
Fields>>cAMP signaling pathway
Gene nameSOX9
Protein nameTranscription factor SOX-9
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID20682
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtQ04887
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID
Rat gene link
Rat Swiss-Prot
Rat Swiss link
ImmunogenThe antiserum was produced against synthesized peptide derived from human SOX-9 around the phosphorylation site of Ser181. AA range:147-196
SpecificityPhospho-Sox-9 (S181) Polyclonal Antibody detects endogenous levels of Sox-9 protein only when phosphorylated at S181.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. Immunofluorescence: 1/200 - 1/1000. ELISA: 1/5000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)65kD
BackgroundSRY-box 9(SOX9) Homo sapiens The protein encoded by this gene recognizes the sequence CCTTGAG along with other members of the HMG-box class DNA-binding proteins. It acts during chondrocyte differentiation and, with steroidogenic factor 1, regulates transcription of the anti-Muellerian hormone (AMH) gene. Deficiencies lead to the skeletal malformation syndrome campomelic dysplasia, frequently with sex reversal. [provided by RefSeq, Jul 2008],
Functiondisease:Defects in SOX9 are the cause of campomelic dysplasia (CMD1) [MIM:114290]. CMD1 is a rare, often lethal, dominantly inherited, congenital osteochondrodysplasia, associated with male-to-female autosomal sex reversal in two-thirds of the affected karyotypic males. A disease of the newborn characterized by congenital bowing and angulation of long bones, unusually small scapulae, deformed pelvis and spine and a missing pair of ribs. Craniofacial defects such as cleft palate, micrognatia, flat face and hypertelorism are common. Various defects of the ear are often evident, affecting the cochlea, malleus incus, stapes and tympanum. Most patients die soon after birth due to respiratory distress which has been attributed to hypoplasia of the tracheobronchial cartilage and small thoracic cage.,function:Plays an important role in the normal skeletal development. May regulate the expression
Subcellular locationNucleus .
ExpressionEye,PNS,Testis,

Additional Images

Image 1
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Western blot analysis of Sox-9 (phospho Ser181) Polyclonal Antibody, using Hela, HepG2 cell treated or untreated with UV, 4° over night, secondary antibody(cat: RS0002 was diluted at 1:10000, 37° 1hour.
Image 2
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Immunofluorescence analysis of A549 cells, using SOX-9 (Phospho-Ser181) Antibody. The picture on the right is blocked with the phospho peptide.
Image 3
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Immunohistochemistry analysis of paraffin-embedded human brain, using SOX-9 (Phospho-Ser181) Antibody. The picture on the right is blocked with the phospho peptide.
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Western blot analysis of lysates from 293 cells treated with PBS 60', using SOX-9 (Phospho-Ser181) Antibody. The lane on the right is blocked with the phospho peptide.
: AO-06-ES7254-50
: 10 Items
Hurry! only 10 items left in stock.

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