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Western Blot (WB) (Western blot analysis of INF2 in (A) human tonsil and (B) rat stomach tissue lysate with INF2 antibody at 1 μg/mL.)

Rabbit anti-Human INF2 Polyclonal Antibody | anti-INF2 antibody

INF2 Antibody

Gene Names
INF2; FSGS5; CMTDIE; pp9484; C14orf151; C14orf173
Reactivity
Human
Applications
ELISA, Western Blot
Purity
Affinity chromatography purified via peptide column.
Synonyms
INF2; Polyclonal Antibody; INF2 Antibody; FSGS5; CMTDIE; C14orf151; C14orf173; anti-INF2 antibody
Ordering
For Research Use Only!
Host
Rabbit
Reactivity
Human
Clonality
Polyclonal
Isotype
IgG
Specificity
INF2 Antibody is predicted to not cross-react with other INF1.
Purity/Purification
Affinity chromatography purified via peptide column.
Form/Format
Liquid
Concentration
1 mg/mL (varies by lot)
Sequence Length
1249
Applicable Applications for anti-INF2 antibody
ELISA (EIA), Western Blot (WB)
Application Notes
Western blot at 1 - 2 mug/mL.
Conjugate
Unconjugated
Immunogen
INF2 antibody was raised against a peptide corresponding to 14 amino acids near the amino terminus of human INF2.
Buffer
INF2 Antibody is supplied in PBS containing 0.02% sodium azide.
Species
Human
Preparation and Storage
Store at 4 degree C for three months and -20 degree C, stable for up to one year.
As with all antibodies care should be taken to avoid repeated freeze thaw cycles
Antibodies should not be exposed to prolonged high temperatures.

Western Blot (WB)

(Western blot analysis of INF2 in (A) human tonsil and (B) rat stomach tissue lysate with INF2 antibody at 1 μg/mL.)

Western Blot (WB) (Western blot analysis of INF2 in (A) human tonsil and (B) rat stomach tissue lysate with INF2 antibody at 1 μg/mL.)
Related Product Information for anti-INF2 antibody
INF2 is a member of the formin family of proteins. It is considered a diaphanous formin due to the presence of a diaphanous inhibitory domain located at the N-terminus of the encoded protein. Studies of a similar mouse protein indicate that the protein encoded by this locus may function in polymerization and depolymerization of actin filaments. Mutations at this locus have been associated with focal segmental glomerulosclerosis 5
Product Categories/Family for anti-INF2 antibody

NCBI and Uniprot Product Information

NCBI GI #
NCBI GeneID
NCBI Accession #
NCBI GenBank Nucleotide #
UniProt Accession #
Molecular Weight
Predicted: 137 kDa
Observed: 160 kDa
NCBI Official Full Name
inverted formin-2 isoform 1
NCBI Official Synonym Full Names
inverted formin, FH2 and WH2 domain containing
NCBI Official Symbol
INF2
NCBI Official Synonym Symbols
FSGS5; CMTDIE; pp9484; C14orf151; C14orf173
NCBI Protein Information
inverted formin-2
UniProt Protein Name
Inverted formin-2
Protein Family
UniProt Gene Name
INF2
UniProt Synonym Gene Names
C14orf151; C14orf173

NCBI Description

This gene represents a member of the formin family of proteins. It is considered a diaphanous formin due to the presence of a diaphanous inhibitory domain located at the N-terminus of the encoded protein. Studies of a similar mouse protein indicate that the protein encoded by this locus may function in polymerization and depolymerization of actin filaments. Mutations at this locus have been associated with focal segmental glomerulosclerosis 5.[provided by RefSeq, Aug 2010]

Uniprot Description

INF2: Severs actin filaments and accelerates their polymerization and depolymerization. Defects in INF2 are the cause of focal segmental glomerulosclerosis type 5 (FSGS5). A renal pathology defined by the presence of segmental sclerosis in glomeruli and resulting in proteinuria, reduced glomerular filtration rate and edema. Renal insufficiency often progresses to end-stage renal disease, a highly morbid state requiring either dialysis therapy or kidney transplantation. Defects in INF2 are the cause of Charcot-Marie-Tooth disease, dominant intermediate type E (CMTDIE). A form of Charcot-Marie-Tooth disease, a disorder of the peripheral nervous system, characterized by progressive weakness and atrophy, initially of the peroneal muscles and later of the distal muscles of the arms. The dominant intermediate type E is characterized by clinical and pathologic features intermediate between demyelinating and axonal peripheral neuropathies, and motor median nerve conduction velocities ranging from 25 to 45 m/sec. Patients additionally manifest focal segmental glomerulonephritis, proteinuria, progression to end- stage renal disease, and a characteristic histologic pattern on renal biopsy. Belongs to the formin homology family. 3 isoforms of the human protein are produced by alternative splicing.

Protein type: Unknown function

Chromosomal Location of Human Ortholog: 14q32.33

Cellular Component: perinuclear region of cytoplasm

Disease: Charcot-marie-tooth Disease, Dominant Intermediate E; Focal Segmental Glomerulosclerosis 5

Research Articles on INF2

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Product Notes

The INF2 inf2 (Catalog #AAA154460) is an Antibody produced from Rabbit and is intended for research purposes only. The product is available for immediate purchase. The INF2 Antibody reacts with Human and may cross-react with other species as described in the data sheet. AAA Biotech's INF2 can be used in a range of immunoassay formats including, but not limited to, ELISA (EIA), Western Blot (WB). Western blot at 1 - 2 mug/mL. Researchers should empirically determine the suitability of the INF2 inf2 for an application not listed in the data sheet. Researchers commonly develop new applications and it is an integral, important part of the investigative research process. It is sometimes possible for the material contained within the vial of "INF2, Polyclonal Antibody" to become dispersed throughout the inside of the vial, particularly around the seal of said vial, during shipment and storage. We always suggest centrifuging these vials to consolidate all of the liquid away from the lid and to the bottom of the vial prior to opening. Please be advised that certain products may require dry ice for shipping and that, if this is the case, an additional dry ice fee may also be required.

Precautions

All products in the AAA Biotech catalog are strictly for research-use only, and are absolutely not suitable for use in any sort of medical, therapeutic, prophylactic, in-vivo, or diagnostic capacity. By purchasing a product from AAA Biotech, you are explicitly certifying that said products will be properly tested and used in line with industry standard. AAA Biotech and its authorized distribution partners reserve the right to refuse to fulfill any order if we have any indication that a purchaser may be intending to use a product outside of our accepted criteria.

Disclaimer

Though we do strive to guarantee the information represented in this datasheet, AAA Biotech cannot be held responsible for any oversights or imprecisions. AAA Biotech reserves the right to adjust any aspect of this datasheet at any time and without notice. It is the responsibility of the customer to inform AAA Biotech of any product performance issues observed or experienced within 30 days of receipt of said product. To see additional details on this or any of our other policies, please see our Terms & Conditions page.

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