TBC14 Antibody (Center)
Affinity Purified Rabbit Polyclonal Antibody (Pab)
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Application
| IHC-P, WB, E |
---|---|
Primary Accession | Q9P2M4 |
Other Accession | NP_001106834.1, NP_001106832.1, NP_065824.2 |
Reactivity | Human, Mouse |
Host | Rabbit |
Clonality | Polyclonal |
Isotype | Rabbit IgG |
Calculated MW | 78137 Da |
Antigen Region | 259-286 aa |
Gene ID | 57533 |
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Other Names | TBC1 domain family member 14, TBC1D14, KIAA1322 |
Target/Specificity | This TBC14 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 259-286 amino acids from the Central region of human TBC14. |
Dilution | WB~~1:1000 IHC-P~~1:50~100 |
Format | Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification. |
Storage | Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. |
Precautions | TBC14 Antibody (Center) is for research use only and not for use in diagnostic or therapeutic procedures. |
Name | TBC1D14 |
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Synonyms | KIAA1322 |
Function | Plays a role in the regulation of starvation-induced autophagosome formation (PubMed:22613832). Together with the TRAPPIII complex, regulates a constitutive trafficking step from peripheral recycling endosomes to the early Golgi, maintaining the cycling pool of ATG9 required for initiation of autophagy. |
Cellular Location | Golgi apparatus, cis-Golgi network. Golgi apparatus, trans-Golgi network Note=After amino acid starvation, Golgi apparatus-associated protein levels increase compared with fed conditions. May be cycling between the Golgi apparatus and an endosomal pool, redistributing to the Golgi apparatus upon starvation |
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Provided below are standard protocols that you may find useful for product applications.
Background
May act as a GTPase-activating protein for Rab family protein(s) (By similarity).
References
Rose, J.E., et al. Mol. Med. 16 (7-8), 247-253 (2010) :
Ishibashi, K., et al. Genes Cells 14(1):41-52(2009)
Tempel, W., et al. Proteins 71(1):497-502(2008)
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