PA550308

Aladin Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PA550308-Each-of-1 In Stock ₹ 46,502.50

PA550308 - Each of 1

₹ 46,502.50

In Stock

Quantity

1

Base Price: ₹ 46,502.50

GST (18%): ₹ 8,370.45

Total Price: ₹ 54,872.95

Antigen

Aladin

Classification

Polyclonal

Conjugate

Unconjugated

Gene

AAAS

Gene Alias

AAA; Aaas; AAASb; achalasia, adrenocortical insufficiency, alacrimia; achalasia, adrenocortical insufficiency, alacrimia (Allgrove, triple-A); ADRACALA; Adracalin; ALADIN; aladin WD repeat nucleoporin; Allgrove, triple-A; D030041N15Rik; GL003

Host Species

Rabbit

Purification Method

Antigen affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

8086

Content And Storage

-20°C

Form

Liquid

Applications

Immunohistochemistry (Paraffin), Western Blot

Concentration

1 mg/mL

Formulation

PBS with 40% glycerol and 0.05% sodium azide; pH 7.4

Gene Accession No.

Q9NRG9

Gene Symbols

AAAS

Immunogen

Fusion protein corresponding to residues near the C terminal of human achalasia, adrenocortical insufficiency, alacrimia

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human

Product Type

Antibody

Isotype

IgG

Related Products

Img

Thermo Scientific

PA550301

--

Img

Thermo Scientific

PA550382

--

Img

Thermo Scientific

PA550338

--

Img

Thermo Scientific

PA550433

--

Img

Thermo Scientific

PA550378

--

Img

Thermo Scientific

PA550874

--

Img

Thermo Scientific

PA550868

--

Img

Thermo Scientific

PA550388

--

Description

  • The antibody detects endogenous levels of total Aladin protein
  • 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.