午夜插插,噜噜噜影院,啪啪伊人网,欧美熟夫,景甜吻戏视频,男人强操性感蕾丝美女视频在线网站,日本美女跳舞视频

Welcome to chemicalbook!
+1 (818) 612-2111
RFQ
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

RFQ
skype
MY Account
Top
Postion:Product Catalog >Coagulation factor XIII B/F13B Protein, Human, Recombinant (His)
Coagulation factor XIII B/F13B  Protein, Human, Recombinant (His)
  • Coagulation factor XIII B/F13B  Protein, Human, Recombinant (His)

Coagulation factor XIII B/F13B Protein, Human, Recombinant (His) NEW

Price $386
Package 50μg
Min. Order:
Supply Ability: 10g
Update Time: 2025-07-21

Product Details

Product Name: Coagulation factor XIII B/F13B Protein, Human, Recombinant (His) Purity: SDS-PAGE: 97.9%; SEC-HPLC: 99.6%
Supply Ability: 10g Release date: 2025/07/21

Product Introduction

Bioactivity

NameCoagulation factor XIII B/F13B Protein, Human, Recombinant (His)
DescriptionCoagulation factor XIII B chain, also known as Fibrin-stabilizing factor B subunit, Protein-glutamine gamma-glutamyltransferase B chain, Transglutaminase B chain and F13B, is a secreted protein which contains 1 Sushi ( CCP / SCR ) domains. Coagulation factor XIII is the last zymogen to become activated in the blood coagulation cascade. Plasma factor XIII is a heterotetramer composed of 2 A subunits and 2 B subunits. The A subunits have catalytic function, and the B subunits do not have enzymatic activity and may serve as a plasma carrier molecules. Platelet factor XIII is composed of just 2 A subunits, which are identical to those of plasma origin. The B chain of factor XIII is not catalytically active, but is thought to stabilize the A subunits and regulate the rate of transglutaminase formation by thrombin. Factor XIII acts as a transglutaminase to catalyze the formation of gamma-glutamyl-epsilon-lysine crosslinking between fibrin molecules, thus stabilizing the fibrin clot. Factor XIII deficiency is classified into two categories: type I deficiency, characterized by the lack of both the A and B subunits; and type II deficiency, characterized by the lack of the A subunit alone. These defects can result in a lifelong bleeding tendency, defective wound healing, and habitual abortion. Defects in F13B are the cause of factor XIII subunit B deficiency ( FA13BD ) which is an autosomal recessive disorder characterized by a life-long bleeding tendency, impaired wound healing and spontaneous abortion in affected women.
StorageShipping with blue ice/Shipping at ambient temperature.

Company Profile Introduction

Target Molecule Corp. (TargetMol) is a global high-tech enterprise, headquartered in Boston, MA, specializing in chemical and biological research product and service to meet the research needs of global customers. TargetMol has evolved into one of the biggest global compound library and small molecule suppliers and a customer based on 40+ countries. TargetMol offers over 80 types of compound libraries and a wide range of high-quality research chemicals including inhibitors, activator, natural compounds, peptides, inhibitory antibodies, and novel life-science kits, for laboratory and scientific use. Besides, virtual screening service is also available for customers who would like to conduct the computer-aided drug discovery.

You may like

Recommended supplier

Product name Price   Suppliers Update time
$1830.00/1mg
VIP2Y
TargetMol Chemicals Inc.
2025-06-24
$451.00/50μg
VIP3Y
TargetMol Chemicals Inc.
2024-11-18
$0.00/10Box
VIP2Y
Shandong Hanjiang Chemical Co., Ltd
2024-10-12
  • Since: 2011-01-07
  • Address: 36 Washington Street, Wellesley Hill, MA
INQUIRY