APOH Polyclonal Antibody #abs115493

APOH Polyclonal Antibody #abs115493

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Description

Catalog-specification

Delivery time

USD price

abs115493-50ul

In Stock

228

Please note that the price provided is for reference purposes only. For specific pricing information, please contact our sales representative, Vecent. Kindly refrain from using ChapGPT-generated content and instead, create unique text that accurately portrays the original message.


Overview

Other names

B2G1;B2GP1;BG

Source

Rabbit

Species Reactivity

Human

Application

WB 1:500 - 1:2000

Immunogen

A fusion protein has been created using a sequence encoding amino acids 21 to 345 of the human apolipoprotein H (APOH) protein (NP_000033.2). This recombinant protein is highly similar to the original APOH sequence and may have therapeutic applications.

Properties

22Rv1

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.
Rephrased: A solution containing 0.02% sodium azide and 50% glycerol in PBS, with a pH of 7.3 and preserved with sodium azide, is the buffer used.

Target

Background

Apolipoprotein H is known to play a role in several physiological processes, including the metabolism of lipoproteins, blood clotting, and the development of antiphospholipid autoantibodies. These autoantibodies are commonly found in the blood of individuals with lupus and primary antiphospholipid syndrome. Interestingly, it appears that APOH may be necessary as a co-factor for the binding of anionic phospholipids by these antiphospholipid autoantibodies in affected patients. However, it is worth noting that APOH does not appear to be crucial for the reactivity of antiphospholipid autoantibodies associated with infections.

Celluar localization

Secreted

UniPort

P02749


Data Examples

19

To analyze extracts of NB4 cells, a Western blot was performed using APOH antibody (abs115493) at a dilution of 1:1000. The lysates/proteins for each lane were 25ug, and the blocking buffer used was 3% nonfat dry milk in TBST. The secondary antibody used was HRP Goat Anti-Rabbit IgG (H+L) at a dilution of 1:10000. This enabled the detection of any APOH protein present in the cell extracts. The Western blot provided valuable insights into the expression level and localization of APOH in NB4 cells.


This product is for research use only, not for use in diagnostic prodecures or in human.


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