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S1700

Sigma-Aldrich

Anti-Synip (N-terminal) antibody produced in rabbit

enhanced validation

~1.5 mg/mL, affinity isolated antibody, buffered aqueous solution

Synonym(s):

Anti-STX4-interacting protein, Anti-STXBP4, Anti-Syntaxin 4-interacting protein, Anti-Syntaxin-binding protein 4

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About This Item

UNSPSC Code:
12352203
NACRES:
NA.41

biological source

rabbit

conjugate

unconjugated

antibody form

affinity isolated antibody

antibody product type

primary antibodies

clone

polyclonal

form

buffered aqueous solution

mol wt

antigen ~65 kDa

species reactivity

human

packaging

antibody small pack of 25 μL

enhanced validation

recombinant expression
Learn more about Antibody Enhanced Validation

concentration

~1.5 mg/mL

technique(s)

western blot: 0.2-0.4 μg/mL using HEK-293T cell lysate expressing human Synip and 0.3-0.6 mg/mL using a HepG2 cell lysate

UniProt accession no.

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

Gene Information

human ... STXBP4(252983)

General description

Syntaxin-4 interacting protein (STXBP4) is also known as synip. It is expressed at high level in insulin-secreting pancreatic β cell line, βHC-9 cells. STXBP4 gene is located on human chromosome 17q22.

Specificity

Anti-Synip (N-terminal) specifically recognizes human Synip.

Application

Anti-Synip (N-terminal) antibody produced in rabbit may be used in immunoblotting.
Applications in which this antibody has been used successfully, and the associated peer-reviewed papers, are given below.
Immunofluorescence (1 paper)

Biochem/physiol Actions

Syntaxin-4 interacting protein (STXBP4) serve as functional links between the insulin signaling cascade and insulin-responsive glucose transporter (GLUT4) vesicles. It interacts with syntaxin 4. Synip inhibits the translocation of GLUT4 from intracellular vesicles to the plasma membrane by binding to syntaxin 4 and preventing the interaction between syntaxin 4 and vesicle-associated membrane protein (VAMP2). STXBP4 can control ΔNp63 ubiquitination. Hence it may act as a squamous cell carcinoma (SCC) biomarker.

Physical form

Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.

Storage and Stability

Store at –20 °C. For continuous use, the product may be stored at 2–8 °C for up to one month. For extended storage, freeze in working aliquots –20 °C. Repeated freezing and thawing, or storage in “frost-free” freezers, is not recommended. If slight turbidity occurs upon prolonged storage, clarify solution by centrifugation before use. Working dilutions should be discarded if not used within 12 hours.

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Storage Class

10 - Combustible liquids

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)


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Synip: A Novel Insulin-Regulated Syntaxin 4-Binding Protein Mediating GLUT4 Translocation in Adipocytes
Min J, et al.
Molecular Cell, 3(6), 751-760 (1999)
STXBP4 drives tumor growth and is associated with poor prognosis through PDGF receptor signaling in lung squamous cell carcinoma
Otaka Y, et al.
Clinical Cancer Research, 23(13), 3442-3452 (2017)
Syntaxin 4 and SYNIP (syntaxin 4 interacting protein) regulate insulin secretion in the pancreatic beta HC-9 cell
Saito T, et al.
The Journal of Biological Chemistry, 278(38), 36718-36725 (2003)
Vidya K Nagalakshmi et al.
Acta physiologica (Oxford, England), 238(4), e14014-e14014 (2023-06-13)
Ureteral obstruction leads to significant changes in kidney renin expression. It is unclear whether those changes are responsible for the progression of kidney damage, repair, or regeneration. In the current study, we aimed to elucidate the contribution of renin-producing cells
D E Korzhevskii et al.
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova, 117(4), 50-55 (2017-06-16)
To determine the cytochemical characteristics of unchanged neurons of the human substantia nigra using a wide range of immunocytochemical markers some of which (glutamate decarboxylase-65, PGP 9.5, non-phosphorylated neurofilament proteins, alpa-tubulin) have never been used for study of human dopaminergic

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