Rabbit NFIX Polyclonal Antibody | anti-NFIX antibody

NFIX-Specific Rabbit Polyclonal

Cat. Num. AAA7601934

• Gene Names: NFIX; NF1A; MRSHSS; SOTOS2
• Reactivity: Human, Mouse, Rat
• Applications: ELISA, Western Blot
• Purity: >=95% as determined by SDS-PAGE; Immunogen Affinity Purified
• Synonyms: NFIX; Polyclonal Antibody; NFIX-Specific Rabbit Polyclonal; anti-NFIX antibody

• Host: Rabbit
• Reactivity: Human, Mouse, Rat
• Clonality: Polyclonal
• Isotype: IgG
• Purity/Purification: >=95% as determined by SDS-PAGE; Immunogen Affinity Purified
• Form/Format: Liquid
• Sequence Length: 440

• Applicable Applications for anti-NFIX antibody: ELISA (EIA), Western Blot (WB)
• Immunogen: Nuclear factor I/X (CCAAT-binding transcription factor)
• Preparation and Storage: PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20 degree C for 24 months (Avoid repeated freeze / thaw cycles.)

Western Blot (WB)

(mouse brain tissue were subjected to SDS PAGE followed by western blot with MBS7601934 (NFIX-Specific antibody) at dilution of 1:500)

NCBI and Uniprot Product Information

• NCBI GI #: 111599728
• NCBI GeneID: 4784
• Molecular Weight: 47,911 Da
• NCBI Official Full Name: NFIX protein
• NCBI Official Synonym Full Names: nuclear factor I X
• NCBI Official Symbol: NFIX
• NCBI Official Synonym Symbols: NF1A; MRSHSS; SOTOS2
• NCBI Protein Information: nuclear factor 1 X-type
• UniProt Protein Name: Nuclear factor 1 X-type
• Protein Family: Nuclear factor
• UniProt Gene Name: NFIX
• UniProt Synonym Gene Names: NF1-X; Nuclear factor 1/X; CTF; NF-I/X; NFI-X
• UniProt Entry Name: NFIX_HUMAN

NCBI Description

The protein encoded by this gene is a transcription factor that binds the palindromic sequence 5'-TTGGCNNNNNGCCAA-3 in viral and cellular promoters. The encoded protein can also stimulate adenovirus replication in vitro. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2012]

Uniprot Description

NFI-X: Recognizes and binds the palindromic sequence 5'- TTGGCNNNNNGCCAA-3' present in viral and cellular promoters and in the origin of replication of adenovirus type 2. These proteins are individually capable of activating transcription and replication. Defects in NFIX are the cause of Sotos syndrome 2 (SOTOS2). A form of Sotos syndrome, a childhood overgrowth syndrome characterized by pre- and postnatal overgrowth, developmental delay, mental retardation, advanced bone age, and abnormal craniofacial morphology. SOTOS2 patients have macrocephaly, long narrow face, high forehead, slender habitus, scoliosis, and unusual behavior characterized especially by anxiety. Defects in NFIX are the cause of Marshall-Smith syndrome (MRSHSS). A distinct malformation syndrome characterized by accelerated skeletal maturation, relative failure to thrive, respiratory difficulties, mental retardation, and unusual facies, including prominent forehead, shallow orbits, blue sclerae, depressed nasal bridge, and micrognathia. Additional skeletal findings include long and thin tubular bones, broad middle phalanges with relatively narrow distal phalanges, and scoliosis. Belongs to the CTF/NF-I family. 5 isoforms of the human protein are produced by alternative splicing.

Protein type: DNA-binding; Transcription factor

Chromosomal Location of Human Ortholog: 19p13.3

Cellular Component: nucleus

Molecular Function: DNA binding; protein binding; RNA polymerase II transcription factor activity, enhancer binding; transcription factor activity

Biological Process: DNA replication; negative regulation of transcription from RNA polymerase II promoter; positive regulation of transcription from RNA polymerase II promoter; transcription from RNA polymerase II promoter

Disease: Marshall-smith Syndrome; Sotos Syndrome 2