CD241 rabbit pAb

CD241 rabbit pAb

AO-06-ES4014-100

CD241 rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES4014
Product nameCD241 rabbit pAb
ReactivityHuman;Rat;Mouse;
ApplicationsWB;IHC;IF;ELISA
Other nameRHAG; RH50; Ammonium transporter Rh type A; Erythrocyte membrane glycoprotein Rh50; Erythrocyte plasma membrane 50 kDa glycoprotein; Rh50A; Rhesus blood group family type A glycoprotein;Rh family type A glycoprotein; Rh type A glycoprotein; Rhesus blood group-associated ammonia channel; Rhesus blood group-associated glycoprotein; CD241
Size100μL
Unit price ($)248
Human gene ID6005
Human Swiss-ProtQ02094
SourceRabbit
IsotypeIgG
TargetCD241
Fields
Gene nameRHAG
Protein nameAmmonium transporter Rh type A
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID19743
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtQ9QUT0
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID65207
Rat gene linkView Rat Gene
Rat Swiss-ProtQ7TNK7
Rat Swiss linkView Rat Swiss-Prot
ImmunogenThe antiserum was produced against synthesized peptide derived from the N-terminal region of human RHAG. AA range:1-50
SpecificityCD241 Polyclonal Antibody detects endogenous levels of CD241 protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. 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)44kD
BackgroundThe protein encoded by this gene is erythrocyte-specific and is thought to be part of a membrane channel that transports ammonium and carbon dioxide across the blood cell membrane. The encoded protein appears to interact with Rh blood group antigens and Rh30 polypeptides. Defects in this gene are a cause of regulator type Rh-null hemolytic anemia (RHN), or Rh-deficiency syndrome.[provided by RefSeq, Mar 2009],
Functiondisease:Defects in RHAG are the cause of regulator type Rh-null hemolytic anemia (RHN) [MIM:268150]; also called Rh-deficiency syndrome. RHN is a form of chronic hemolytic anemia in which the red blood cells have a stomatocytosis and spherocytosis morphology, an increased osmotic fragility, an altered ion transport system, and abnormal membrane phospholipid organization.,function:Associated with rhesus blood group antigen expression. May be part of an oligomeric complex which is likely to have a transport or channel function in the erythrocyte membrane.,similarity:Belongs to the ammonium transporter (TC 2.A.49) family. Rh subfamily.,subunit:Heterotetramer.,tissue specificity:Erythrocytes.,
Subcellular locationMembrane ; Multi-pass membrane protein.
ExpressionErythrocytes.

Additional Images

Image 1
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Western Blot analysis of K562 cells using CD241 Polyclonal Antibody. Secondary antibody(catalog#:RS0002) was diluted at 1:20000
Image 2
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Immunohistochemical analysis of paraffin-embedded human-liver, antibody was diluted at 1:100
Image 3
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Immunohistochemical analysis of paraffin-embedded human-liver, antibody was diluted at 1:100
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Immunohistochemical analysis of paraffin-embedded human-brain, antibody was diluted at 1:100
: AO-06-ES4014-100
: 10 Produits
Hurry! only 10 items left in stock.

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