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MYH9 Antibody

MYH9 Antibody

Item no.	PRS-59-654-400ul
Manufacturer	ProSci
Amount	400 ul
Category	Oncology Antibodies Western Blot Primary Antibodies By Organ Colorectal Cancer
Type	Antibody Polyclonal
Format	Liquid
Applications	WB
Specific against	Human, Mouse
Host	Rabbit
ECLASS 10.1	32160702
ECLASS 11.0	32160702
UNSPSC	12352203
Alias	Myosin-9, Cellular myosin heavy chain, type A, Myosin heavy chain 9, Myosin heavy chain, non-muscle IIa, Non-muscle myosin heavy chain A, NMMHC-A, Non-muscle myosin heavy chain IIa, NMMHC II-a, NMMHC-IIA, MYH9
Available
Shipping	blue ice or RT
By Research Area	Signal Transduction
Immunogen	This MYH9 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 1840-1867 amino acids from the C-terminal region of human MYH9.
Applications	For WB starting dilution is: 1:2000
Predicted Molecular Weight	227 kDa
Purification	This antibody is purified through a protein A column, followed by peptide affinity purification.
Clonality	Polyclonal
Isotype	Rabbit Ig
Conjugate	Unconjugated
Buffer	Supplied in PBS with 0.09% (W/V) sodium azide.
Concentration	batch dependent
Storage Conditions	Store at 4˚ C for three months and -20˚ 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.
Disclaimer	Optimal dilutions/concentrations should be determined by the end user. The information provided is a guideline for product use. This product is for research use only.
Modifications	None
Ncbi Official Symbol	MYH9
Accession #	P35579
Protein Gi #	6166599
Ncbi Gene Id #	4627
User Note	Optimal dilutions for each application to be determined by the researcher.
Ncbi Official Symbol	MYH9
Ncbi Official Full Name	Myosin-9
Ncbi Organism	Homo sapiens
Swissprot #	P35579
Background	This gene encodes a myosin IIA heavy chain that containsan IQ domain and a myosin head-like domain. The protein is involvedin several important functions, including cytokinesis, cellmotility and maintenance of cell shape. Defects in MYH9 are thecause of non-syndromic sensorineural deafness autosomal dominanttype 17, Epstein syndrome, Alport syndrome withmacrothrombocytopenia, Sebastian syndrome, Fechtner syndrome andmacrothrombocytopenia with progressive sensorineural deafness.
Background References 1	Arii, J., et al. Nature 467(7317):859-862(2010)
Background References 2	Genovese, G., et al. Kidney Int. 78(7):698-704(2010)
Background References 3	Tzur, S., et al. Hum. Genet. 128(3):345-350(2010)
Background References 4	Bostrom, M.A., et al. Hum. Genet. 128(2):195-204(2010)
1st Image Caption	Western Blot at 1:2000 dilution + mouse kidney lysate Lysates/proteins at 20 ug per lane.
2nd Image Caption	Western Blot at 1:2000 dilution Lane 1: A431 whole cell lysate Lane 2: Hela whole cell lysate Lane 3: HT-29 whole cell lysate Lysates/proteins at 20 ug per lane.

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

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Amount: 400 ul

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Delivery expected until 9/6/2024

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