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| Cat.No | ACP00101 | Target Name | RAB27A |
|---|---|---|---|
| Target Synonyms | Rab-27;GTP-binding protein Ram | Form | Liquid or Lyophilized powder |
| Expression System | Yeast | Expression Range | 2-221aa |
| Mol Weight | 26.2 kDa | Protein Length | Full Length of Mature Protein |
| Purity | Greater than 95% as determined by SDS-PAGE. | Storage Buffer | 5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0. |
| Target Species | Human | Uniprot ID | P51159 |
|---|
Uniprot Id
P51159
Target Species
Human
Target Name
RAB27A
Target Full Name
Ras-related protein Rab-27A
Target Function
Small GTPase which cycles between active GTP-bound and inactive GDP-bound states. In its active state, binds to a variety of effector proteins to regulate homeostasis of late endocytic pathway, including endosomal positioning, maturation and secretion. Plays a role in cytotoxic granule exocytosis in lymphocytes. Required for both granule maturation and granule docking and priming at the immunologic synapse.
Target Involvement
Griscelli syndrome 2 (GS2)
Target Subcellular Location
Membrane; Lipid-anchor. Melanosome. Late endosome. Lysosome.
Target Protein Families
Small GTPase superfamily, Rab family
Target Tissue Specificity
Found in all the examined tissues except in brain. Low expression was found in thymus, kidney, muscle and placenta. Detected in melanocytes, and in most tumor cell lines examined. Expressed in cytotoxic T-lymphocytes (CTL) and mast cells.
Target Research Area
Signal Transduction
Target Synonyms
GS2; GTP-binding protein Ram; HsT18676; MGC117246; Mutant Ras related protein Rab-27A; Rab-27; RAB-27A; RAB27; RAB27A; RAB27A member RAS oncogene family; RAM; Ras-related protein Rab-27A; Ras-related protein Rab27A; RB27A_HUMAN
Target Background
The protein encoded by this gene belongs to the small GTPase superfamily, Rab family. The protein is membrane-bound and may be involved in protein transport and small GTPase mediated signal transduction. Mutations in this gene are associated with Griscelli syndrome type 2. Alternative splicing occurs at this locus and four transcript variants encoding the same protein have been identified.
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