AP3D1 antibody (AA 520-700)

Catalog No. ABIN6136969

The Rabbit Polyclonal anti-AP3D1 antibody has been validated for WB. It is suitable to detect AP3D1 in samples from Human.

Quick Overview for AP3D1 antibody (AA 520-700) (ABIN6136969)

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

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This AP3D1 antibody is un-conjugated

Application: Western Blotting (WB)

Product Details anti-AP3D1 Antibody

Binding Specificity: AA 520-700

Sequence: AVYVQNVVKL YASILQQKEQ AGEAEGAQAV TQLMVDRLPQ FVQSADLEVQ ERASCILQLV KHIQKLQAKD VPVAEEVSAL FAGELNPVAP KAQKKVPVPE GLDLDAWINE PLSDSESEDE RPRAVFHEEE QRRPKHRPSE ADEEELARRR EARKQEQANN PFYIKSSPSP QKRYQDTPGV E

Cross-Reactivity: Human, Mouse

Characteristics: Polyclonal Antibodies

Purification: Affinity purification

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 520-700 of human AP3D1 (NP_003929.4).

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 AP3D1

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

Alternative Name: AP3D1

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.,AP3D1,ADTD,HPS10,hBLVR,Signal Transduction,AP3D1

Molecular Weight: 111 kDa/114 kDa/125 kDa/130 kDa/136 kDa

Gene ID: 8943

UniProt: O14617