AP3D1 antibody

Catalog No. ABIN6292609

Product Details anti-AP3D1 Antibody

Target: AP3D1 (Adaptor-Related Protein Complex 3, delta 1 Subunit (AP3D1))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This AP3D1 antibody is un-conjugated

Application: Western Blotting (WB)

Purification: Affinity purification

Immunogen: Recombinant Protein of human AP3D1

Isotype: IgG

Application Details

Application Notes: WB 1:500 - 1:2000

Comment:

Present in all adult tissues examined with the highest levels in skeletal muscle, heart, pancreas and testis

Restrictions: For Research Use only

Handling

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 -20C. Avoid freeze / thaw cycles.

Target Details for AP3D1

Target: AP3D1 (Adaptor-Related Protein Complex 3, delta 1 Subunit (AP3D1))

Alternative Name: AP3D1 (AP3D1 Products)

Synonyms: wu:fj51g01 antibody, si:ch211-129c21.6 antibody, ADTD antibody, hBLVR antibody, AA407035 antibody, Ap3d antibody, Bolvr antibody, mBLVR1 antibody, mh antibody, mocha antibody, BLVR antibody, adaptor-related protein complex 3, delta 1 subunit antibody, AP-3 complex subunit delta-1 antibody, adaptor related protein complex 3 delta 1 subunit antibody, ap3d1 antibody, EDI_172030 antibody, EHI_158840 antibody, Tsp_04773 antibody, AP3D1 antibody, Ap3d1 antibody

Background: The protein encoded by this gene is a subunit of the AP3 adaptor-like complex, which is not clathrin-associated, but is associated with the golgi region, as well as more peripheral structures. The AP-3 complex facilitates the budding of vesicles from the golgi membrane, and may be directly involved in trafficking to lysosomes. This subunit is implicated in intracellular biogenesis and trafficking of pigment granules, and possibly platelet dense granules and neurotransmitter vesicles. Defects in this gene are a cause of a new type of Hermansky-Pudlak syndrome.

Molecular Weight: 130.158 kDa

Gene ID: 8943

UniProt: O14617