ELK Biotechnology
HNF-4α (Acetyl Lys106) Rabbit Polyclonal Antibody - ES8628
HNF-4α (Acetyl Lys106) Rabbit Polyclonal Antibody - ES8628
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HNF-4α (Acetyl Lys106) Rabbit Polyclonal Antibody
Sizes: 50μL, 100μL
Catalogue Numbers: ES8628-50, ES8628-100
Lead times: 1-2 weeks, if manufacturer has product in stock
Manufacturer/Ship Location: China
Background: The protein encoded by this gene is a nuclear transcription factor which binds DNA as a homodimer. The encoded protein controls the expression of several genes, including hepatocyte nuclear factor 1 alpha, a transcription factor which regulates the expression of several hepatic genes. This gene may play a role in development of the liver, kidney, and intestines. Mutations in this gene have been associated with monogenic autosomal dominant non-insulin-dependent diabetes mellitus type I. Alternative splicing of this gene results in multiple transcript variants encoding several different isoforms. [provided by RefSeq, Apr 2012],
Reactivity: Human, Rat, Mouse
Host: Rabbit
Applications: WB, ELISA
Alternate Names: Hepatocyte nuclear factor 4-alpha (HNF-4-alpha) (Nuclear receptor subfamily 2 group A member 1) (Transcription factor 14) (TCF-14) (Transcription factor HNF-4)
Clonality: Polyclonal
Immunogen: Synthetic Acetyl peptide from human protein at AA range: 106
Isotype: IgG
Target: HNF4α
Specificity: The antibody detects endogenous HNF-4α when Acetyl occurs at Lys106
Dilution: WB 1:500-2000, ELISA 1:10000-20000
Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration: 1 mg/ml,
Formlation: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Expression: Kidney, Liver,
Observed Band (KD): 55kD
Fields: AMPK signaling pathway, Maturity onset diabetes of the young
Function: Alternative Products: Additional isoforms seem to exist,Disease: Defects in HNF4A are the cause of maturity onset diabetes of the young type 1 (MODY1) [MIM: 125850], also shortened MODY-1. MODY [MIM: 606391] is a form of diabetes that is characterized by an autosomal dominant mode of inheritance, onset in childhood or early adulthood (usually before 25 years of age) and a primary defect in insulin secretion. The clinical phenotype of MODY1 is characterized by severe insulin secretory defects, and by major hyperglycemia associated with microvascular complications
Function: Transcriptionally controlled transcription factor. Binds to DNA sites required for the transcription of alpha 1-antitrypsin, apolipoprotein CIII, transthyretin genes and HNF1-alpha. May be essential for development of the liver, kidney and intestine
Miscellaneous: Binds fatty acids
Online Information: Hepatocyte nuclear fac
Subcellular Location: Nucleus
Storage and Stability: -20°C/1 year
Gene Name: HNF4A HNF4 NR2A1 TCF14
Protein Name: Hepatocyte nuclear factor 4-alpha (HNF-4-alpha) (Nuclear receptor subfamily 2 group A member 1) (Transcription factor 14) (TCF-14) (Transcription factor HNF-4)
Mouse SwissProt Number: P49698
Rat SwissProt Number: P22449
Research Use Only
