4.1R rabbit pAb

4.1R rabbit pAb

AO-06-ES5123-100

4.1R rabbit pAb 100μL

check En Stock
Hurry! only 10 items left in stock.
429,00 €
HT
Quantité

Antibody Product Overview

ELK.NoES5123
Product name4.1R rabbit pAb
ReactivityHuman;Mouse
ApplicationsWB;ELISA
Other nameEPB41; E41P; Protein 4.1; P4.1; 4.1R; Band 4.1; EPB4.1
Size100μL
Unit price ($)248
Human gene ID2035
Human Swiss-ProtP11171
SourceRabbit
IsotypeIgG
Target4.1R
Fields
Gene nameEPB41
Protein nameProtein 4.1
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID269587
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtP48193
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 EPB41. AA range:626-675
Specificity4.1R Polyclonal Antibody detects endogenous levels of 4.1R protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. 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)60kD
BackgroundThe protein encoded by this gene, together with spectrin and actin, constitute the red cell membrane cytoskeletal network. This complex plays a critical role in erythrocyte shape and deformability. Mutations in this gene are associated with type 1 elliptocytosis (EL1). Alternatively spliced transcript variants encoding different isoforms have been described for this gene.[provided by RefSeq, Oct 2009],
Functiondisease:Defects in EPB41 are a cause of hereditary pyropoikilocytosis (HPP) [MIM:266140]. HPP is an autosomal recessive hematologic disorder characterized by hemolytic anemia, microspherocytosis, poikilocytosis, and an unusual thermal sensitivity of red cells.,disease:Defects in EPB41 are the cause of elliptocytosis type 1 (EL1) [MIM:611804]. EL1 is a Rhesus-linked form of hereditary elliptocytosis, a genetically heterogeneous, autosomal dominant, hematologic disorder. It is characterized by variable hemolytic anemia and elliptical or oval red cell shape.,function:Protein 4.1 is a major structural element of the erythrocyte membrane skeleton. It plays a key role in regulating membrane physical properties of mechanical stability and deformability by stabilizing spectrin-actin interaction. Recruits DLG1 to membranes.,PTM:O-glycosylated; contains N-acetylglucosamine side chains in the C-ter
Subcellular locationCytoplasm, cytoskeleton . Cytoplasm, cell cortex . Nucleus .
ExpressionBrain,PCR rescued clones,Reticulocyte,Spleen,

Additional Images

Image 1
No image
Western blot analysis of lysates from HepG2 cells treated with PMA 125ng/ml 30', using EPB41 Antibody. The lane on the right is blocked with the synthesized peptide.
No image
No image
No image
: AO-06-ES5123-100
: 10 Produits
Hurry! only 10 items left in stock.

Use collapsible tabs for more detailed information that will help customers make a purchasing decision.

Ex: Shipping and return policies, size guides, and other common questions.

  • Paste the label on a flat surface on the package
  • Make sure that both 1D and 2D barcodes are clearly visible
  • Ensure that the label is smooth and isn’t creased or wrinkled
  • Check for any tears, dents, holes or scratches
  • Pack your product tightly, with the right size packaging
  • Ensure both barcodes are on a flat surface of the package