PDX-1 rabbit pAb

PDX-1 rabbit pAb

AO-06-ES5913-50

PDX-1 rabbit pAb 50μL

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Antibody Product Overview

ELK.NoES5913
Product namePDX-1 rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;IHC
Other namePDX1; IPF1; Pancreas/duodenum homeobox protein 1; PDX-1; Glucose-sensitive factor; GSF; Insulin promoter factor 1; IPF-1; Insulin upstream factor 1; IUF-1; Islet/duodenum homeobox-1; IDX-1; Somatostatin-transactivating factor 1; STF-1
Size50μL
Unit price ($)148
Human gene ID3651
Human Swiss-ProtP52945
SourceRabbit
IsotypeIgG
TargetPDX1
Fields>>Insulin secretion;>>Type II diabetes mellitus;>>Maturity onset diabetes of the young
Gene namePDX1
Protein namePancreas/duodenum homeobox protein 1
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID18609
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtP52946
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID29535
Rat gene linkView Rat Gene
Rat Swiss-ProtP52947
Rat Swiss linkView Rat Swiss-Prot
ImmunogenThe antiserum was produced against synthesized peptide derived from human PDX1. AA range:27-76
SpecificityPDX-1 Polyclonal Antibody detects endogenous levels of PDX-1 protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWB 1:500-2000;IHC-p 1:50-300
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)42kD
BackgroundThe protein encoded by this gene is a transcriptional activator of several genes, including insulin, somatostatin, glucokinase, islet amyloid polypeptide, and glucose transporter type 2. The encoded nuclear protein is involved in the early development of the pancreas and plays a major role in glucose-dependent regulation of insulin gene expression. Defects in this gene are a cause of pancreatic agenesis, which can lead to early-onset insulin-dependent diabetes mellitus (NIDDM), as well as maturity onset diabetes of the young type 4 (MODY4). [provided by RefSeq, Jul 2008],
Functiondisease:Defects in PDX1 are a cause of pancreatic agenesis [MIM:260370]. This autosomal recessive disorder is characterized by absence or hypoplasia of pancreas, leading to early-onset insulin-dependent diabetes mellitus. This was found in a frameshift mutation that produces a truncated protein and results in a second initiation that produces a second protein that act as a dominant negative mutant.,disease:Defects in PDX1 are the cause of maturity onset diabetes noninsulin-dependent diabetes mellitus (NIDDM) [MIM:125853]; also known as diabetes mellitus type II.,disease:Defects in PDX1 are the cause of maturity onset diabetes of the young type 4 (MODY4) [MIM:606392]; also symbolized MODY-4. MODY [MIM:606391] is a form of diabetes mellitus characterized by an autosomal dominant mode of inheritance, age of onset of 25 years or younger and a primary defect in insulin secretion.,domain:The A
Subcellular locationNucleus. Cytoplasm, cytosol .
ExpressionDuodenum and pancreas (Langerhans islet beta cells and small subsets of endocrine non-beta-cells, at low levels in acinar cells).

Additional Images

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Western blot analysis of lysates from PC12 cells, primary antibody was diluted at 1:1000, 4°over night
Image 2
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Immunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).
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: AO-06-ES5913-50
: 10 Items
Hurry! only 10 items left in stock.

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