anti- ALADIN antibody

Delve into the world of alacrima, achalasia, and adrenal insufficiency syndrome (ALADIN) with our highly specialized Anti-ALADIN Antibody, now available in a convenient 100µg size.

ALADIN is a key component of the nuclear pore complex, and mutations in the ALADIN gene are associated with a rare autosomal recessive disorder known as triple A syndrome. Our antibody is meticulously crafted to provide unparalleled specificity and sensitivity, making it an ideal choice for various applications, from immunohistochemistry to co-immunoprecipitation and more.

What truly distinguishes our Anti-ALADIN Antibody is its outstanding performance. Rigorously tested and validated, it ensures consistent and reproducible results, effectively reducing experimental variability and saving you valuable time and resources.

With a 100µg size, this product strikes the perfect balance between cost-effectiveness and practicality, offering ample antibody for multiple experiments while minimizing wastage. This aligns with our commitment to sustainable research practices.

Engineered for user-friendliness, our Anti-ALADIN Antibody is suitable for researchers at all levels, from novices to seasoned experts. It seamlessly integrates into various laboratory techniques, enhancing the precision and reliability of your experiments.

Empower your research with confidence, knowing you have the support of a high-quality, meticulously crafted Anti-ALADIN Antibody. Step into the forefront of scientific discovery in nuclear pore biology and genetic disorders with this essential tool and contribute to groundbreaking insights in the field.

Product Name

ALADIN antibody

Size

100µg

Form

liquid

Purification

Immunogen affinity purified

Purity

≥95% as determined by SDS-PAGE

Host

Rabbit

Clonality

polyclonal

Isotype

IgG

Storage

PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20℃ for 12 months (Avoid repeated freeze / thaw cycles.)

BACKGROUND

The protein encoded by this gene is a member of the WD-repeat family of regulatory proteins and may be involved in normal development of the peripheral and central nervous system. The encoded protein is part of the nuclear pore complex and is anchored there by NDC1. Defects in this gene are a cause of achalasia-addisonianism-alacrima syndrome (AAAS), also called triple-A syndrome or Allgrove syndrome. Two transcript variants encoding different isoforms have been found for this gene.

IMMUNOGEN INFORMATION

Immunogen

achalasia, adrenocortical insufficiency, alacrimia (Allgrove, triple-A)

Synonyms

AAA, AAAS, AAASb, ADRACALA, ADRACALIN, ALADIN, DKFZp586G1624, GL003

Observed MW

60 kDa

APPLICATION

Tested Application

ELISA, WB, IHC, IF

Recommended Dilution

WB: 1:500 - 1:2000; IHC: 1:50 - 1:200; IF: 1:50 - 1:200

UNIPROT INFORMATION

UniProt ID

Q9NRG9

IMAGES