PIGM Antibody

Code CSB-PA017976GA01HU
Size $600
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Product Details

Uniprot No.
Target Names
PIGM
Alternative Names
PIGM antibody; GPI mannosyltransferase 1 antibody; EC 2.4.1.- antibody; GPI mannosyltransferase I antibody; GPI-MT-I antibody; Phosphatidylinositol-glycan biosynthesis class M protein antibody; PIG-M antibody
Raised in
Rabbit
Species Reactivity
Human,Mouse,Rat
Immunogen
Human PIGM
Immunogen Species
Homo sapiens (Human)
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, pH 7.3. -20°C, Avoid freeze / thaw cycles.
Tested Applications
ELISA,WB,IHC
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.

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Target Background

Function
Mannosyltransferase involved in glycosylphosphatidylinositol-anchor biosynthesis. Transfers the first alpha-1,4-mannose to GlcN-acyl-PI during GPI precursor assembly.
Gene References into Functions
  1. B cells but not red cells are glycosylphosphatidylinositol deficient in PIGM-associated inherited glycosylphosphatidylinositol deficiency, caused by a core promoter mutation that abrogates Sp1 binding. PMID: 25293775
  2. Studies indicate that mutations in PGM1 by exome sequencing cause hypoglycemia and liver abnormalities. PMID: 23329837
  3. Mutation substantially reduces transcription of PIGM and blocks mannosylation of glycosylphosphatidylinositol(GPI), leading to partial but severe deficiency of GPI. PMID: 16767100
Involvement in disease
Glycosylphosphatidylinositol deficiency (GPID)
Subcellular Location
Endoplasmic reticulum membrane; Multi-pass membrane protein.
Protein Families
PIGM family
Database Links

HGNC: 18858

OMIM: 610273

KEGG: hsa:93183

STRING: 9606.ENSP00000357069

UniGene: Hs.552810

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