Anti-Proinsulin monoclonal antibody (DMABT-H4145MH)

Mouse Anti-Human Proinsulin monoclonal antibody for EIA, IHC-Fr, Pr*

Specifications


Host Species
Mouse
Antibody Isotype
IgG1
Clone
5C3
Species Reactivity
Human
Immunogen
Purified human proinsulin
Conjugate
Unconjugated

Applications


Application Notes
EIA, IHC-Fr, Pr*
We recommend the following for sandwich ELISA (Capture - Detection):
DMABT-H4145MH - DMAB3823MH
*Suggested working dilutions are given as a guide only. It is recommended that the user titrates the product for use in their own experiment using appropriate negative and positive controls.

Target


Alternative Names
INS; insulin; proinsulin; ILPR; IRDN; IDDM2
Entrez Gene ID
UniProt ID

Product Background


Pathway
ATF-2 transcription factor network, organism-specific biosystem; Adipogenesis, organism-specific biosystem; Aldosterone-regulated sodium reabsorption, organism-specific biosystem; Aldosterone-regulated sodium reabsorption, conserved biosystem; Amyloids, organism-specific biosystem; Arf6 trafficking events, organism-specific biosystem; Developmental Biology, organism-specific biosystem;

Citations


Have you cited DMABT-H4145MH in a publication? Let us know and earn a reward for your research.

Custom Antibody Labeling


We offer labeled antibodies using our catalogue antibody products and a broad range of intensely fluorescent dyes and labels including HRP, biotin, ALP, Alexa Fluor® dyes, DyLight® Fluor dyes, R-phycoerythrin (R-PE), at scales from less than 100 μg up to 1 g of IgG antibody. Learn More

Customer Reviews


Write a review, share your experiences with others and get rewarded !
Product Name Cat. No. Applications Host Species Datasheet Price Add to Basket

References


Ferroelectric low-voltage ON/OFF switching of chiral benzene-1,3,5-tricarboxamide derivative

JOURNAL OF MATERIALS CHEMISTRY C

Authors: Wu, Jianyun; Takeda, Takashi; Hoshino, Norihisa; Akutagawa, Tomoyuki

The phase transition behaviour, molecular assemblies, and dielectric responses of a nN,N ',N ''-trialkylbenzene-1,3,5-tricarboxamide derivative bearing chiral (S)-3,7-dimethyloctyl chains (S-3BC) were compared with those of anN,N ',N ''-trioctadecylbenzene-1,3,5-tricarboxamide derivative (3BC) bearing achiral -CONHC(14)H(29)chains. ChiralS-3BCshowed a similar phase transition behaviour to achiral3BC, and ferroelectric polarization-electric field (P-E) hysteresis curves were observed in the discotic hexagonal columnar (Col(h)) liquid crystal phase. Interestingly, the magnitudes ofP(r)andE(t)values ofS-3BCwere 5.5-times larger and 13-times smaller than those of3BCbecause of the introduction of the chiral alkyl chains, indicating a useful method to obtain low voltage ON/OFF ratios for the switching device. Much stronger N-H center dot center dot center dot O = hydrogen-bonding interactions were observed inS-3BCthan in3BCbecause of much shorter pi-stacking distance and blue-shift of the intermolecular asymmetrical N-H vibrational band in the former, which effectively decreased the potential energy barrier for the dipole inversion between N-H center dot center dot center dot O = and = O center dot center dot center dot H-N orientations and theE(t)value.

Application of enzyme-assisted extraction of baicalin fromScutellaria baicalensisGeorgi

PREPARATIVE BIOCHEMISTRY & BIOTECHNOLOGY

Authors: Ma, Xiao-Di; Zhang, Xin-Guo; Guo, Si-Jia; Ma, Guo-Yan; Liu, Wen-Jie; Wang, Nan; Feng, Ming; Su, Yu

Endophytes may depend on degrading the plant cell wall with cellulases for their survival. Therefore, cellulase produced by endophytes may be useful in releasing the active ingredient of medicinal plants.Scutellaria baicalensisGeorgi is a traditional Chinese medicinal plant widely used in China and baicalin is one of its main active ingredients. In this study, freshS. baicalensisGeorgi was used to isolate endophytes, Congo red staining was used to screen cellulase-producing strains, and HPLC was used to determine the content of baicalin inS. baicalensisGeorgi. As a result, a highly active strain of endophyte capable of the extraction of high levels of baicalin was obtained. The strain was named HG-5 and identified asBacillussp. Scanning electron microscopy analysis confirmed that the enzyme better promotes the dissolution of plant active ingredients. After optimizing the enzyme production and extraction processes, we found that when compared with the traditional extraction method, the baicalin yield was increased 79.31% after extraction with the HG-5 enzyme. The current study provides a novel approach and method for the use of endophyte cellulase to improve the extraction of compounds from medicinal plants.

Online Inquiry

Name:
Phone: *
E-mail Address: *
Technology Interest:
Type of Organization:
Service & Products Interested: *
Project Description:
Verification code
Click image to refresh the verification code.

Online Inquiry

  Interested in larger quantities ? request a quote!
  Protocol may be improved. Please feel free to contact us to obtain the latest version.!

Ordering Information

Payment methods we support:
Invoice / Purchase Order
Credit card

OUR PROMISE TO YOU Guaranteed product quality expert customer support

Inquiry Basket