Hipersensibilidade Imediata (Tipo I): A Resposta Imune É Mediada Por Células Th2

Lab Reagents

Hipersensibilidade Laboratories manufactures the hipersensibilidade imediata (tipo i): a resposta imune é mediada por células th2 reagents distributed by Genprice. The Hipersensibilidade Imediata (Tipo I): A Resposta Imune É Mediada Por Células Th2 reagent is RUO (Research Use Only) to test human serum or cell culture lab samples. To purchase these products, for the MSDS, Data Sheet, protocol, storage conditions/temperature or for the concentration, please contact Hipersensibilidade. Other Hipersensibilidade products are available in stock. Specificity: Hipersensibilidade Category: Imediata Group: (Tipo I):

(Tipo I): information

POR Antibody
47179-100ul 100ul
EUR 252

Human Colon Cancer Primer Library I
HCCP-I 1 set
EUR 548

Human DNA Repair Primer Library I
HDRL-I 1 set
EUR 548

Human Drug Transporter I Primer Library
HDTP-I 1 set
EUR 548

Mouse DNA Repair Primer Library I
MDRL-I 1 set
EUR 645

Human Interferon Type I Signaling Primer Library
HIFN-I 1 set
EUR 548

Human Cancer Driver Gene I Primer Library
HCDG-I 1 set
EUR 645

anti-Apolipoprotein A-I (Apo A-I) (1D8)
LF-MA0377 100 ul
EUR 334
Description: Mouse monoclonal to Apolipoprotein A-I (Apo A-I)

anti-Apolipoprotein A-I (Apo A-I) (10E9)
LF-MA0379 100 ul
EUR 334
Description: Mouse monoclonal to Apolipoprotein A-I (Apo A-I)

anti-Apolipoprotein A-I (Apo A-I) (26H8)
LF-MA0380 100 ul
EUR 334
Description: Mouse monoclonal to Apolipoprotein A-I (Apo A-I)

Apolipoprotein A-I
MO27002 20 ug
EUR 318

Apolipoprotein A-I
PR27175 20 ug
EUR 186

POR cloning plasmid
CSB-CL018378HU-10ug 10ug
EUR 682
Description: A cloning plasmid for the POR gene.

pCMV-SPORT6-POR
PVT14093 2 ug
EUR 391

POR Polyclonal Antibody
A57874 100 µg
EUR 570.55
Description: The best epigenetics products

Anti-POR antibody
STJ110441 100 µl
EUR 413
Description: This gene encodes an endoplasmic reticulum membrane oxidoreductase with an FAD-binding domain and a flavodoxin-like domain. The protein binds two cofactors, FAD and FMN, which allow it to donate electrons directly from NADPH to all microsomal P450 enzymes. Mutations in this gene have been associated with various diseases, including apparent combined P450C17 and P450C21 deficiency, amenorrhea and disordered steroidogenesis, congenital adrenal hyperplasia and Antley-Bixler syndrome.

POR Conjugated Antibody
C47179 100ul
EUR 397