MABS1713MI

MilliporeSigma™ Synaptotagmin-like Protein 4 (SYTL4), Mouse, Unlabeled, Clone: 7D2.2,

Manufacturer: MilliporeSigma™

Select a Size

Pack Size SKU Availability Price
Each of 1 MABS1713MI-Each-of-1 In Stock ₹ 38,958.86

MABS1713MI - Each of 1

₹ 38,958.86

In Stock

Quantity

1

Base Price: ₹ 38,958.86

GST (18%): ₹ 7,012.595

Total Price: ₹ 45,971.455

Antigen

Synaptotagmin-like Protein 4 (SYTL4)

Classification

Monoclonal

Concentration

Please refer to lot specific datasheet.

Formulation

Purified mouse IgG2aκ in buffer containing 0.1M Tris-Glycine (pH 7.4), 150mM NaCl with 0.05% Sodium Azide.

Gene Accession No.

Q96C24

Immunogen

GST-tagged recombinant human synaptotagmin-like protein 4 (SYTL4) internal fragment.

Quantity

100 μg

Research Discipline

Signaling

Gene ID (Entrez)

NP_001123368

Target Species

Human

Form

Purified

Applications

Western Blot

Clone

7D2.2

Conjugate

Unconjugated

Gene

SYTL4, SLP4

Host Species

Mouse

Purification Method

Protein G Purified

Regulatory Status

RUO

Primary or Secondary

Primary

Test Specificity

Clone 7D2.2 epitope resides within an internal region mostly missing in human spliced isoform 2. Reactivity toward isoform 2 has not been confirmed.

Content And Storage

Stable for 1 year at 2°-8°C from date of receipt.

Isotype

IgG2a κ

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Description

  • Synaptotagmin-like protein 4 (UniProt Q96C24; also known as Exophilin-2, Granuphilin) is encoded by the SYTL4 (also known as SLP4) gene (Gene ID 94121) in human
  • SYLT4 belongs to the synaptotagmin-like protein family, which contains an N-terminal RabBD (Rab-binding) domain and two C-terminal C2 domains
  • The characteristic feature of this family is the N-terminal domain, which is not found in other C-type tandem C2 proteins
  • SYLT4 is detected close to the plasma membrane and on secretory granules
  • Interacts with vesicles containing negatively charged phospholipids in a Ca2+-independent manner
  • It can bind to both the GTP- and GDP-bound forms of Rab27A and inhibits a specific GTP/GDP exchange cycle required for dense-core vesicle exocytosis
  • It is the first regulatory in the exocytosis pathway that functions by directly connecting Rab and SNARE
  • It modulates exocytosis of dense-core granules and secretion of hormones in the pancreas and the pituitary
  • It is not only essential for the docking of insulin granules, but also simultaneously imposes a fusion constraint on them through an interaction with syntaxin-1alpha fusion machinery.