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Anti-ANKRD26 Antibody (aa1-15) LS-C19104


Wt. Vol. Conc. Price
100 µg - - Unavailable

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Rabbit Polyclonal to Mouse ANKRD26
Western blot, ELISA


Mouse ANKRD26
Mouse (tested or 100% immunogen sequence identity)
Immunoaffinity purified


  • Western blot (1:500 - 1:3000)
  • ELISA (1:20000 - 1:80000)

Specificity and Use

ANKRD26 antibody was raised against synthetic peptide from mouse ANKRD26.
Amino acids 1-15 of mouse Ankrd26 protein.
This affinity purified antibody has been tested for use in ELISA and by western blot. Specific conditions for reactivity should be optimized by the end user. Expect a band approximately 81 kD in size corresponding to Ankrd26 by western blotting in the appropriate mouse tissue.


0.02 M potassium phosphate, 0.15 M sodium chloride, pH 7.2, 0.01% sodium azide.
Store vial at -20 C prior to opening. Dilute only prior to immediate use. For extended storage aliquot contents and freeze at -20 C or below. Avoid cycles of freezing and thawing.
For research use only.

About ANKRD26

Q9UPS8 AB028997 BAA83026.2

ANKRD26 Antibody, BA145E8.1 Antibody, KIAA1074 Antibody, THC2 Antibody, Ankyrin repeat domain 26 Antibody

ANKRD26 encodes a protein containing N-terminal ankyrin repeats which function in protein-protein interactions. Mutations in this gene are associated with autosomal dominant thrombocytopenia-2. Pseudogenes of this gene are found on chromosome 7, 10, 13 and 16. Multiple transcript variants encoding different isoforms have been found for this gene.

Western blot

Western blot
Anti-Ankrd26 Antibody - Western Blot. Western blot of affinity purified anti-Ankrd26 antibody shows detection of a band at ~81 kD corresponding to mouse Ankrd26 protein. Lane 1 Blank, Lane 2 MES cell lysate - 80 ug, Lane 3 MES cell lysate - 40 ug, Lane 4 293T-ANKRD26 transfected cell lysate - 20 ug, Lane 5 control 293T cell lysate - 20 ug, Lane 6 BSA-ANKRD26 conjugate 20 ng, Lane 7 BSA - 500 ng, Lane 8 BSA - 100 ng, Lane 9 BSA 20 ng and Lane 10 Protein standards. Detection of endogenous Ankrd26 protein in MES cell lysates may occur when detection methods with higher sensitivity are used. Proteins were separated by SDS-PAGE, transferred to nitrocellulose, and probed with the primary antibody diluted to 1:1000 followed by detection using ALP conjugated Gt-a-Rabbit IgG (LS-C60866 is suggested) diluted to 1:3000. Size estimation was made by comparison to prestained MW markers as indicated. Personal Communication. Ira Pastan, NIH, CCR, Bethesda, MD.

Requested From: 
Date Requested: 3/25/2017

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