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Purified Mouse Anti-Adaptin γ
Purified Mouse Anti-Adaptin γ

Western blot analysis of Adaptin γ on PC12 cell lysate.  Lane 1: 1:5000, lane 2: 1:10000, lane 3: 1:20000 dilution of anti-Adaptin γ.

Purified Mouse Anti-Adaptin γ

Immunofluorescent staining of Rat Neurons with anti-Adaptin γ antibody.

Western blot analysis of Adaptin γ on PC12 cell lysate.  Lane 1: 1:5000, lane 2: 1:10000, lane 3: 1:20000 dilution of anti-Adaptin γ.

Immunofluorescent staining of Rat Neurons with anti-Adaptin γ antibody.

Product Details
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BD Transduction Laboratories™
Rat (QC Testing), Human, Mouse, Dog (Tested in Development)
Mouse IgG2a
Mouse Adaptin γ aa. 642-821
Western blot (Routinely Tested), Immunofluorescence, Immunohistochemistry, Immunoprecipitation (Tested During Development)
104 kDa
250 µg/ml
Aqueous buffered solution containing BSA, glycerol, and ≤0.09% sodium azide.

Preparation And Storage

Store undiluted at -20°C. The monoclonal antibody was purified from tissue culture supernatant or ascites by affinity chromatography.

Product Notices

  1. Since applications vary, each investigator should titrate the reagent to obtain optimal results.
  2. Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before discarding to avoid accumulation of potentially explosive deposits in plumbing.
  3. Sodium azide is a reversible inhibitor of oxidative metabolism; therefore, antibody preparations containing this preservative agent must not be used in cell cultures nor injected into animals. Sodium azide may be removed by washing stained cells or plate-bound antibody or dialyzing soluble antibody in sodium azide-free buffer. Since endotoxin may also affect the results of functional studies, we recommend the NA/LE (No Azide/Low Endotoxin) antibody format, if available, for in vitro and in vivo use.
  4. Source of all serum proteins is from USDA inspected abattoirs located in the United States.
  5. Please refer to for technical protocols.
610386 Rev. 2
Antibody Details
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88/Adaptin γ

Sorting of integral membrane proteins at various stages of the endocytic and secretory pathways is mediated by vesicular trafficking between a variety of organelles. Two sorting signals are tyrosine-based and dileucine-based signals that interact with heterotetrameric adaptor protein complexes (AP-1, AP-2, AP-3, and AP-4), which are associated with the vesicle coats. These coatomers contain two large Adaptin proteins (γ, α, δ, or ε and β1, β2, β3, or β4, respectively) that are noncovalently linked to one medium chain (µ1, µ2, µ3, or µ4) and one small chain ( σ1, σ2, σ3, or σ4). The AP-1 and AP-3 complexes are involved in protein sorting from the TGN and endosomes, while AP-2 adaptor complexes are involved in clathrin-mediated endocytosis. Adaptin γ shows more homology with Adaptin α than with Adaptin β. The conserved regions between Adaptins γ and α could be important for binding to other components of the AP-1 and AP-2 complexes, respectively.

610386 Rev. 2
Format Details
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Tissue culture supernatant is purified by either protein A/G or affinity purification methods. Both methods yield antibody in solution that is free of most other soluble proteins, lipids, etc. This format provides pure antibody that is suitable for a number of downstream applications including: secondary labeling for flow cytometry or microscopy, ELISA, Western blot, etc.
610386 Rev.2
Citations & References
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Development References (5)

  1. Eskelinen EL, Illert AL, Tanaka Y. Role of LAMP-2 in lysosome biogenesis and autophagy. Mol Biol Cell. 2002; 13(9):3355-3368. (Clone-specific: Electron microscopy). View Reference
  2. Kalthoff C, Groos S, Kohl R, Mahrhold S, Ungewickell EJ. Clint: a novel clathrin-binding ENTH-domain protein at the Golgi. Mol Biol Cell. 2002; 13(11):4060-4073. (Clone-specific: Immunoprecipitation). View Reference
  3. Nagahama M, Suzuki M, Hamada Y, et al. SVIP is a novel VCP/p97-interacting protein whose expression causes cell vacuolation. Mol Biol Cell. 2003; 14(1):262-273. (Clone-specific: Immunofluorescence). View Reference
  4. Robinson MS. Cloning and expression of gamma-adaptin, a component of clathrin-coated vesicles associated with the Golgi apparatus. J Cell Biol. 1990; 111(6 Pt 1):2319-2326. (Biology). View Reference
  5. Wasiak S, Legendre-Guillemin V, Puertollano R, et al. Enthoprotin: a novel clathrin-associated protein identified through subcellular proteomics. J Cell Biol. 2002; 158(5):855-862. (Clone-specific: Immunofluorescence, Western blot). View Reference
View All (5) View Less
610386 Rev. 2

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