PA540232

Phospho-EPB41 (Tyr660) Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PA540232-Each-of-1 In Stock ₹ 48,104.50

PA540232 - Each of 1

₹ 48,104.50

In Stock

Quantity

1

Base Price: ₹ 48,104.50

GST (18%): ₹ 8,658.81

Total Price: ₹ 56,763.31

Antigen

Phospho-EPB41 (Tyr660)

Classification

Polyclonal

Conjugate

Unconjugated

Gene

EPB41

Gene Alias

4.1R; AI415518; Band 4.1; D4Ertd442e; E41P; EL1; elliptocytosis 1, RH-linked; Elp1; Elp-1; EPB4.1; EPB41; erythrocyte membrane protein band 4.1; erythrocyte membrane protein band 4.1 (elliptocytosis 1, RH-linked); erythrocyte protein band 4.1; erythrocyte skeletal protein; erythrocyte surface protein band 4.1; HE; Kiaa4056; mKIAA4056; P4.1; protein 4.1; Protein 4.1R; RGD1564762

Host Species

Rabbit

Purification Method

Antigen affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

2035, 269587

Content And Storage

-20° C, Avoid Freeze/Thaw Cycles

Form

Liquid

Applications

ELISA, Immunohistochemistry, Western Blot

Concentration

1 mg/mL

Formulation

PBS with 0.5% BSA, 50% glycerol and 0.02% sodium azide; pH 7.4

Gene Accession No.

P11171, P48193

Gene Symbols

EPB41

Immunogen

Synthesized peptide derived from human 4.1R around the phosphorylation site of Y660.

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human, Mouse

Product Type

Antibody

Isotype

IgG

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Description

  • This antibody is predicted to react with mouse based on sequence homology
  • Elliptocytosis is a hematologic disorder characterized by elliptically shaped erythrocytes and a variable degree of hemolytic anemia
  • Inherited as an autosomal dominant, elliptocytosis results from mutation in any one of several genes encoding proteins of the red cell membrane skeleton
  • The form discussed here is the one found in the 1950s to be linked to Rh blood group and more recently shown to be caused by a defect in protein 4
  • 1
  • 'Rh-unlinked' forms of elliptocytosis are caused by mutation in the alpha-spectrin gene, the beta-spectrin gene, or the band 3 gene.