Adracalin antibody (AA 287-546)

Catalog No. ABIN6136308

Product Details anti-Adracalin Antibody

Target: Adracalin (AAAS) (Achalasia, Adrenocortical Insufficiency, Alacrimia (AAAS))

Binding Specificity: AA 287-546

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Adracalin antibody is un-conjugated

Application: Western Blotting (WB)

Sequence: GGGVTNLLWS PDGSKILATT PSAVFRVWEA QMWTCERWPT LSGRCQTGCW SPDGSRLLFT VLGEPLIYSL SFPERCGEGK GCVGGAKSAT IVADLSETTI QTPDGEERLG GEAHSMVWDP SGERLAVLMK GKPRVQDGKP VILLFRTRNS PVFELLPCGI IQGEPGAQPQ LITFHPSFNK GALLSVGWST GRIAHIPLYF VNAQFPRFSP VLGRAQEPPA GGGGSIHDLP LFTETSPTSA PWDPLPGPPP VLPHSPHSHL

Cross-Reactivity: Human

Characteristics: Polyclonal Antibodies

Purification: Affinity purification

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 287-546 of human AAAS (NP_056480.1).

Isotype: IgG

Application Details

Application Notes: WB,1:500 - 1:2000

Comment:

HIGH QUALITY

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for Adracalin

Target: Adracalin (AAAS) (Achalasia, Adrenocortical Insufficiency, Alacrimia (AAAS))

Alternative Name: AAAS (AAAS Products)

Synonyms: zgc:85873 antibody, aladin antibody, Aladin antibody, AAA antibody, AAASb antibody, ADRACALA antibody, ADRACALIN antibody, ALADIN antibody, D030041N15Rik antibody, GL003 antibody, aladin WD repeat nucleoporin antibody, achalasia, adrenocortical insufficiency, alacrimia antibody, aladin WD repeat nucleoporin L homeolog antibody, Aaas antibody, aaas antibody, aaas.L antibody, AAAS antibody

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.,AAAS,AAA,AAASb,ADRACALA,ADRACALIN,ALADIN,GL003,aladin,Neuroscience,AAAS

Molecular Weight: 55 kDa/59 kDa

Gene ID: 8086

UniProt: Q9NRG9