GTX32019
AP3M1 antibody
Cannot supply to this region.
- SKU:
- GTX32019
- Additional Names:
- adaptor related protein complex 3 subunit mu 1
- Application:
- ELISA, WB, IHC-P
- Concentration:
- 1 mg/ml
- Physical State:
- Liquid
- Species Reactivity:
- Human
- Purification:
- Affinity Purified
- Storage Conditions:
- -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
- Supplier:
- Genetex
- Host:
- Rabbit
- Reactivities:
- Human, Mouse, Rat
- Buffer:
- PBS, 0.02% Sodium azide.
- Immunogen:
- AP3M1 antibody was raised against a 15 amino acid synthetic peptide near the carboxy terminus of human AP3M1.The immunogen is located within amino acids 340 - 390 of AP3M1.
- Uniprot:
- Q9Y2T2
- Synonyms:
- adapter-related protein complex 3 mu-1 subunit;adaptor related protein complex 3 mu 1 subunit;Adaptor-related protein complex 3 subunit mu-1;AP-3 adapter complex mu3A subunit;AP-3 adaptor complex mu3A subunit;AP-3 complex subunit mu-1;clathrin adaptor complex AP3, mu-3A subunit;mu-adaptin 3A;mu3A-adaptin
- Extra Details:
- The protein encoded by this gene is the medium subunit of AP-3, which is an adaptor-related protein complex associated with the Golgi region as well as more peripheral intracellular structures. AP-3 facilitates the budding of vesicles from the Golgi membrane and may be directly involved in protein sorting to the endosomal/lysosomal system. AP-3 is a heterotetrameric protein complex composed of two large subunits (delta and beta3), a medium subunit (mu3), and a small subunit (sigma 3). Mutations in one of the large subunits of AP-3 have been associated with the Hermansky-Pudlak syndrome, a genetic disorder characterized by defective lysosome-related organelles. Alternatively spliced transcript variants encoding the same protein have been observed. [provided by RefSeq, Jul 2008]
- Shipping Conditions:
- Blue Ice