PSPH Polyclonal Antibody #abs118216

abs118216-50ul

In Stock

228

Other names

PSP;PSPHD

Source

Rabbit

Species Reactivity

Human;Mouse;Rat

Application

WB 1:500 - 1:2000
IHC 1:50 - 1:200

Immunogen

PSPH1-225（NP_004568.2）。，。

Properties

Some of the cell lines used in research laboratories include HeLa, Jurkat, and A-431. Other commonly studied tissues include mouse brain, mouse testis, and rat liver. Additionally, HepG2 and U-251MG cells are often utilized in various experiments. These diverse samples provide researchers with valuable insights into a wide array of biological processes and pathways. The ability to study different tissues and cell types has greatly expanded our understanding of human physiology and the mechanisms underlying diseases. Ongoing research efforts continue to shed light on these important topics, and new discoveries are constantly emerging as a result.

Properties

Purification

Affinity purification

Clonality

Polyclonal Antibody

Isotype

IgG

Stability & Storage

Store at -20℃. Avoid freeze / thaw cycles.

Storage buffer

Store at -20℃. Avoid freeze / thaw cycles.
A solution of PBS containing 0.02% sodium azide and 50% glycerol at a pH of 7.3 is known to us as buffer.

Target

Background

The gene in question encodes a protein that belongs to a specific subgroup of phosphotransferases. This particular enzyme is responsible for the final step in the production of L-serine. Its primary function involves the hydrolysis of L-phosphoserine, a process that relies on the presence of magnesium. Additionally, this enzyme is also involved in a reciprocal reaction between L-serine and L-phosphoserine. Research suggests that a deficiency of this protein may potentially be associated with Williams syndrome. Altering the presentation, I would say something like:

Part of a larger family of phosphotransferases, this gene's protein product plays a crucial role within its own subcategory. Specifically, it acts as an enzyme responsible for the third and final stage in the formation of L-serine. By catalyzing the hydrolysis of L-phosphoserine, this protein relies on magnesium and plays a key role. Furthermore, it takes part in an exchange reaction involving L-serine and L-phosphoserine. Perturbations in the functioning of this protein have been hypothesized to be connected to Williams syndrome.

UniPort

P78330