STXBP5L Antibodies

AND STXBP5L ELISA kits, STXBP5L Proteins

Many biological assays use antibodies to detect STXBP5L, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with STXBP5L in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop STXBP5L antibodies...

We validate the specificity of these antibodies to STXBP5L by testing them on tissues known to express STXBP5L positively and negatively. Browse below to find the STXBP5L antibody that suites your experiment. We have 0 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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STXBP5L Infographic by Boster Bio

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STXBP5L Overview

Facts about Syntaxin-binding protein 5-like.

STXBP5L 3D structure. Source: alphafold

Syntaxin-binding protein 5-like (STXBP5L)

May play a role in vesicle trafficking and exocytosis. .

Gene Information

Human
Gene Name:	STXBP5L
Uniprot:	Q9Y2K9
Entrez:	9515

Family

Belongs to:

WD repeat L(2)GL family

Alternative Names

Syntaxin-binding protein 5-like

Molecular Weight

Mass (kDA):
131.887 kDA

Genomic Context


Human

Location:	3q13.33
Sequence:	3; NC_000003.12 (120908205..121424761)

Tissue Specificity

Detected in kidney, hippocampus and lung carcinoma.

Subcellular Localizations

Cytoplasm. Cell membrane; Peripheral membrane protein. Membrane; Peripheral membrane protein. Cytoplasmic, and associated with vesicular membranes and the plasma membrane.

PTMs

Acetylation
Methylation

Phosphoprotein
Ubl conjugation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/STXBP5L

References

PMID: 14767561 by Katoh M., et al. Identification and characterization of human LLGL4 gene and mouse Llgl4 gene in silico.

PMID: 25504045 by Kumar R., et al. Homozygous mutation of STXBP5L explains an autosomal recessive infantile-onset neurodegenerative disorder.