AP2S1 Recombinant antibody, PBS Only

AP2S1 Uni-rAbTM Recombinant Antibody for WB, IHC, IF/ICC, Indirect ELISA
Cat No. 84174-3-PBS
Clone No.241369F1

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse, rat

Applications

WB, IHC, IF/ICC, Indirect ELISA

AP17 DELTA, AP17, AP 2 complex subunit sigma, Adaptor-related protein complex 2 subunit sigma, Adaptor protein complex AP-2 subunit sigma

Formulation:  PBS Only
PBS and Azide
PBS Only
Conjugate:  Unconjugated
Size/Concentration: 

-/ -

Freight/Packing: -

Quantity

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Product Information

84174-3-PBS targets AP2S1 in WB, IHC, IF/ICC, Indirect ELISA applications and shows reactivity with human, mouse, rat samples.

Tested Reactivity human, mouse, rat
Host / Isotype Rabbit / IgG
Class Recombinant
Type Antibody
Immunogen AP2S1 fusion protein Ag8095 Predict reactive species
Full Name adaptor-related protein complex 2, sigma 1 subunit
Calculated Molecular Weight 142 aa, 17 kDa
Observed Molecular Weight15-17 kDa
GenBank Accession NumberBC006337
Gene Symbol AP2S1
Gene ID (NCBI) 1175
Conjugate Unconjugated
Form Liquid
Purification MethodProtein A purfication
UNIPROT IDP53680
Storage Buffer PBS Only
Storage ConditionsStore at -80°C.

Background Information

AP2S1 is a component of the adaptor protein complex 2 (AP-2). AP complexes are cytosolic heterotetramers that mediate the sorting of membrane proteins in the secretory and endocytic pathways. AP complexes form clathrin-coated vesicles (CCVs) by recruiting the scaffold protein, clathrin. AP complexes also play a pivotal role in cargo selection by recognizing the sorting signals within the cytoplasmic tail of integral membrane proteins. AP-2 is composed of two large adaptins (alpha-type subunit AP2A1 or AP2A2 and beta-type subunit AP2B1), a medium adaptin (mu-type subunit AP2M1), and a small adaptin (sigma-type subunit AP2S1). It works on the plasma membrane to internalize cargo in clathrin-mediated endocytosis. Missense mutations of AP2S1 affect Arg15 and lead to familial hypocalciuric hypercalcemia type 3 (FHH3), an extracellular calcium homeostasis disorder affecting the parathyroids, kidneys, and bone (PMID: 23222959).

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