MESP1 Antibody

Code CSB-PA871559ESR2HU
Size US$166
Order now
Image
  • Immunohistochemistry of paraffin-embedded human pancreatic tissue using CSB-PA871559ESR2HU at dilution of 1:100

  • Immunohistochemistry of paraffin-embedded human pancreatic cancer using CSB-PA871559ESR2HU at dilution of 1:100

Have Questions? Leave a Message or Start an on-line Chat

Product Details

Full Product Name
Rabbit anti-Homo sapiens (Human) MESP1 Polyclonal antibody
Uniprot No.
Target Names
MESP1
Alternative Names
bHLHc5 antibody; Class C basic helix-loop-helix protein 5 antibody; Mesoderm posterior 1 antibody; Mesoderm posterior 1 homolog (mouse) antibody; Mesoderm posterior 1 homolog antibody; Mesoderm posterior protein 1 antibody; MESP 1 antibody; Mesp1 antibody; MESP1_HUMAN antibody; MGC10676 antibody; MGC159208 antibody; MGC159210 antibody; OTTMUSP00000030151 antibody
Raised in
Rabbit
Species Reactivity
Human
Immunogen
Recombinant Human Mesoderm posterior protein 1 protein (149-268AA)
Immunogen Species
Homo sapiens (Human)
Conjugate
Non-conjugated
Clonality
Polyclonal
Isotype
IgG
Purification Method
Antigen Affinity Purified
Concentration
It differs from different batches. Please contact us to confirm it.
Buffer
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Form
Liquid
Tested Applications
ELISA, IHC
Recommended Dilution
Application Recommended Dilution
IHC 1:20-1:200
Troubleshooting and FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time
Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.

Customer Reviews and Q&A

 Customer Reviews

There are currently no reviews for this product.

Submit a Review here

Target Background

Function
Transcription factor. Plays a role in the epithelialization of somitic mesoderm and in the development of cardiac mesoderm. Defines the rostrocaudal patterning of the somites by participating in distinct Notch pathways.
Gene References into Functions
  1. The present study firstly provided experimental evidence supporting the concept that a MESP1 lossoffunction mutation may contribute to the development of double outlet right ventricle in humans, which presents a significant insight into the molecular pathogenesis of congenital heart disease. PMID: 28677747
  2. results suggest that pathologic variants in MESP1 may contribute to the development of congenital heart disease (CHD) and that additional protein partners and downstream targets could likewise contribute to the wide range of causes for CHD PMID: 26694203
  3. The MESP1-NKX2-5 hESC reporter line allows us to identify molecular cues crucial for specification and expansion of human cardiac mesoderm and early progenitors and their differentiation to specific cardiovascular derivatives. PMID: 25187301
  4. MESP1 SNPs are associated with congenital heart disease in patients and altered transcription in vitro. PMID: 24056064
  5. Transcription factors ETS2 and MESP1 transdifferentiate human dermal fibroblasts into cardiac progenitors. PMID: 22826236
  6. MesP1 drives vertebrate cardiovascular differentiation through Dkk-1-mediated blockade of Wnt-signalling PMID: 18297060

Show More

Hide All

Subcellular Location
Nucleus.
Database Links

HGNC: 29658

OMIM: 608689

KEGG: hsa:55897

STRING: 9606.ENSP00000300057

UniGene: Hs.447531

icon of phone
Call us
301-363-4651 (Available 9 a.m. to 5 p.m. CST from Monday to Friday)
icon of address
Address
7505 Fannin St., Ste 610, Room 7 (CUBIO Innovation Center), Houston, TX 77054, USA
icon of social media
Join us with

Subscribe newsletter

Leave a message

* To protect against spam, please pass the CAPTCHA test below.
CAPTCHA verification
© 2007-2024 CUSABIO TECHNOLOGY LLC All rights reserved. 鄂ICP备15011166号-1
Place an order now

I. Product details

*
*
*
*

II. Contact details

*
*

III. Ship To

*
*
*
*
*
*
*

IV. Bill To

*
*
*
*
*
*
*
*