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SMARCAL1 Antibody

ArtNr PRS-28-999-100ul
Hersteller ProSci
Menge 100 ul
Kategorie
Typ Antibody Polyclonal
Format Liquid
Applikationen WB, ELISA
Specific against Human, Rat
Host Rabbit
ECLASS 10.1 32160702
ECLASS 11.0 32160702
UNSPSC 12352203
Alias SMARCAL1, HARP, HHARP
Lieferbar
Shipping
blue ice or RT
By Research Area
Transcription
Immunogen
Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human SMARCAL1.
Applications
SMARCAL1 antibody can be used for detection of SMARCAL1 by ELISA at 1:312500. SMARCAL1 antibody can be used for detection of SMARCAL1 by western blot at 1.25 μ g/mL, and HRP conjugated secondary antibody should be diluted 1:50, 000 - 100, 000.
Positive Control 1
721_B Cell Lysate
Predicted Molecular Weight
106 kDa
Purification
Antibody is purified by protein A chromatography method.
Clonality
Polyclonal
Conjugate
Unconjugated
Buffer
Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
Concentration
batch dependent
Storage Conditions
For short periods of storage (days) store at 4˚ C. For longer periods of storage, store SMARCAL1 antibody at -20˚ C. As with any antibody avoid repeat freeze-thaw cycles.
Disclaimer
This product is for research use only.
Modifications
None
Ncbi Official Symbol
SMARCAL1
Accession #
NP_054859
Protein Gi #
21071060
Ncbi Gene Id #
50485
User Note
Optimal dilutions for each application to be determined by the researcher.
Ncbi Official Symbol
SMARCAL1
Ncbi Official Full Name
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1
Ncbi Organism
Homo sapiens
Swissprot #
Q9NZC9
Background
SMARCAL1 is a member of the SWI/SNF family of proteins. Members of this family have helicase and ATPase activities and are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. Mutations in SMARCAL1 gene are a cause of Schimke immunoosseous dysplasia (SIOD), an autosomal recessive disorder with the diagnostic features of spondyloepiphyseal dysplasia, renal dysfunction, and T-cell immunodeficiency.The protein encoded by this gene is a member of the SWI/SNF family of proteins. Members of this family have helicase and ATPase activities and are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. The encoded protein shows sequence similarity to the E. coli RNA polymerase-binding protein HepA. Mutations in this gene are a cause of Schimke immunoosseous dysplasia (SIOD), an autosomal recessive disorder with the diagnostic features of spondyloepiphyseal dysplasia, renal dysfunction, and T-cell immunodeficiency.
Background References 1
Clewing, J.M., (2007) Hum. Mutat. 28 (3), 273-283.
1st Image Caption
Antibody used in WB on Human 721_B at 1.25 ug/ml.

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Alle Produkte sind nur für Forschungszwecke bestimmt. Nicht für den menschlichen, tierärztlichen oder therapeutischen Gebrauch.

Menge: 100 ul
Lieferbar: In stock
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