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The antibody against STX16 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 1-300 of human STX16 (NP_001128244.1) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.
The antibody against STX16 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 1-300 of human STX16 (NP_001128244.1) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.
| Cat.No | ADA-01757A | Clonality | Polyclonal |
|---|---|---|---|
| Host Species | Rabbit | Target Name | STX16 |
| Target Synonyms | SYN16; SYN-16; STX16 | Form | Liquid |
| Species Reactivity | Human | Isotype | IgG |
| Storage Buffer | 50% Glycerol, PBS with 0.02% sodium azide, pH7.3. | Purification Method | Affinity purification |
| Positive Samples | MCF7, SH-SY5Y, SKOV3 | Application | ELISA, WB |
| Immunogen Description | Recombinant fusion protein containing a sequence corresponding to amino acids 1-300 of human STX16 (NP_001128244.1). | Target Species | Human |
|---|---|---|---|
| Uniprot ID | O14662 | Immunogen Sequence |
Uniprot Id
O14662
Target Species
Human
Target Name
STX16
Target Full Name
Syntaxin-16
Target Function
SNARE involved in vesicular transport from the late endosomes to the trans-Golgi network.
Target Involvement
Pseudohypoparathyroidism 1B (PHP1B)
Target Subcellular Location
Golgi apparatus membrane; Single-pass type IV membrane protein.; [Isoform C]: Cytoplasm.
Target Protein Families
Syntaxin family
Target Tissue Specificity
Ubiquitous.
Target Synonyms
STX16; Syntaxin-16; Syn16
Target Background
This gene encodes a protein that is a member of the syntaxin or t-SNARE (target-SNAP receptor) family. These proteins are found on cell membranes and serve as the targets for V-SNARES (vesicle-SNAP receptors) permitting specific synaptic vesicle docking and fusion. A microdeletion in the region of chromosome 20 where this gene is located has been associated with pseudohypoparathyroidism type Ib. Multiple transcript variants have been found for this gene. Read-through transcription also exists between this gene and the neighboring downstream aminopeptidase-like 1 (NPEPL1) gene.
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