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  • Featured Product
  • KD/KO Validated

CoraLite® Plus 488-conjugated MGP Polyclonal antibody

MGP Polyclonal Antibody for IF-P

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse

Applications

IF-P

Conjugate

CoraLite® Plus 488 Fluorescent Dye

Cat no : CL488-10734

Print datasheet

Synonyms

GIG36, matrix Gla protein, MGLAP, MGP, NTI

验证数据展示

  • IF Staining of mouse liver using CL488-10734

    IF Staining of mouse liver using CL488-10734

    Immunofluorescent analysis of (4% PFA) fixed paraffin-embedded mouse liver tissue using CoraLite® Plus 488 MGP antibody (CL488-10734) at dilution of 1:200. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0).

经过测试的应用

Positive IF-P detected inmouse liver tissue
For other applications, we recommend the unconjugated version of this antibody, 10734-1-AP

推荐稀释比

ApplicationDilution
Immunofluorescence (IF)-PIF-P : 1:50-1:500
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

产品信息

CL488-10734 targets MGP in IF-P applications and shows reactivity with human, mouse samples.

Tested Applications IF-P Application Description
Tested Reactivity human, mouse
Immunogen MGP fusion protein Ag1091 种属同源性预测
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Full Name matrix Gla protein
Synonyms GIG36, matrix Gla protein, MGLAP, MGP, NTI
Calculated Molecular Weight 103 aa, 13 kDa
GenBank Accession NumberBC005272
Gene Symbol MGP
Gene ID (NCBI) 4256
Conjugate CoraLite® Plus 488 Fluorescent Dye
Excitation/Emission Maxima Wavelengths493 nm / 522 nm
Form Liquid
Purification MethodAntigen affinity purification
UNIPROT IDP08493
Storage Buffer PBS with 50% Glycerol, 0.05% Proclin300, 0.5% BSA, pH 7.3.
Storage ConditionsStore at -20°C. Avoid exposure to light. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

背景介绍

Matrix Gla protein (MGP), a vitamin K-dependent protein, is recognized as a calcification inhibitor in vascular tissue. Defects in MGP are the cause of Keutel syndrome (KS), which is an autosomal recessive disorder characterized by abnormal cartilage calcification, peripheral pulmonary stenosis neural hearing loss and midfacial hypoplasia.

实验方案

Product Specific Protocols
IF protocol for CL Plus 488 MGP antibody CL488-10734Download protocol
Standard Protocols
Click here to view our Standard Protocols