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  • KD/KO Validated

GMPPB Polyclonal antibody

GMPPB Polyclonal Antibody for WB, IHC, IF/ICC, ELISA

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse, rat and More (1)

Applications

WB, IHC, IF/ICC, ELISA

Conjugate

Unconjugated

Cat no : 15094-1-AP

Synonyms

Mannose-1-phosphate guanyltransferase beta, KIAA1851, GTP-mannose-1-phosphate guanylyltransferase beta, GDP-mannose pyrophosphorylase B, EC:2.7.7.13


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Tested Applications

Positive WB detected inmouse skeletal muscle tissue, mouse brain tissue, rat brain tissue
Positive IHC detected inhuman ovary cancer tissue
Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0
Positive IF/ICC detected inHEK-293 cells

Recommended dilution

ApplicationDilution
Western Blot (WB)WB : 1:200-1:1000
Immunohistochemistry (IHC)IHC : 1:50-1:500
Immunofluorescence (IF)/ICCIF/ICC : 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.

Product Information

15094-1-AP targets GMPPB in WB, IHC, IF/ICC, ELISA applications and shows reactivity with human, mouse, rat samples.

Tested Reactivity human, mouse, rat
Cited Reactivityhuman, mouse, zebrafish
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen GMPPB fusion protein Ag7168 相同性解析による交差性が予測される生物種
Full Name GDP-mannose pyrophosphorylase B
Calculated molecular weight 40 kDa
Observed molecular weight 40-43 kDa
GenBank accession numberBC001141
Gene symbol GMPPB
Gene ID (NCBI) 29925
RRIDAB_2111064
Conjugate Unconjugated
Form Liquid
Purification MethodAntigen affinity purification
Storage Buffer PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
Storage ConditionsStore at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

Background Information

GMPPB is a cytoplasmic enzyme that catalyzes the formation of GDP-mannose, a key substrate for several glycosylation pathways, including O-mannosylation of α-DG. GMPPB facilitates the formation of the sugar donor GDP-mannose and pyrophosphate from mannose-1-phosphate and GTP, a very early step in the glycosylation pathway (PMID: 37834154, 27147698). GMPPB mutations correlate with several congenital diseases, including severe congenital muscular dystrophy (CMD) with abnormalities in the brain and eye (PMID: 26310427, 30684953). Western blot analysis detected GMPPB at an apparent molecular mass of 40 kDa.

Protocols

Product Specific Protocols
WB protocol for GMPPB antibody 15094-1-APDownload protocol
IHC protocol for GMPPB antibody 15094-1-APDownload protocol
IF protocol for GMPPB antibody 15094-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols

Publications

SpeciesApplicationTitle
humanWB

iScience

A Trace Amount of Galactose, a Major Component of Milk Sugar, Allows Maturation of Glycoproteins during Sugar Starvation.

Authors - Norio Sasaoka
mouseWB

Front Mol Biosci

Altered Glycosylation in the Aging Heart.

Authors - Patricia Franzka
zebrafishWB

Mol Biomed

GMPPB-congenital disorders of glycosylation associate with decreased enzymatic activity of GMPPB.

Authors - Zhe Liu
human,mouseWB

Front Nutr

Altered mannose metabolism in chronic stress and depression is rapidly reversed by vitamin B12

Authors - Patricia Franzka
humanWB,IHC

Int J Mol Sci

Silencing GMPPB Inhibits the Proliferation and Invasion of GBM via Hippo/MMP3 Pathways

Authors - Zi-Lu Huang
  • KD Validated
mouseWB,IF

Front Mol Neurosci

Consequences of GMPPB deficiency for neuromuscular development and maintenance

Authors - Mona K Schurig