Recombinant MYL9 Antibody - Primary antibody, specific to MYL9, Rabbit IgG

Features and benefits
  • Short Overview:

    Recombinant; Rabbit anti Human MYL9 Antibody; WB; Unconjugated

  • Species reactivity(Reacts with): Human,Mouse,Rat
  • Isotype: Rabbit IgG
    Application:
  • WB
Item Number
Ab116779
Grouped product items
SKUSizeAvailabilityPrice Qty
Ab116779-10μl
10μl
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$69.90
Ab116779-50μl
50μl
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$199.90
Ab116779-100μl
100μl
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$309.90
Ab116779-1ml
1ml
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$2,799.90

Recombinant; Rabbit anti Human MYL9 Antibody; WB; Unconjugated

Basic Description

Product NameRecombinant MYL9 Antibody - Primary antibody, specific to MYL9, Rabbit IgG
Synonyms20 kDa myosin light chain | LC20 | MLC-2C | Myosin regulatory light chain 2, smooth muscle isoform | Myosin regulatory light chain 9 | Myosin regulatory light chain MRLC1 | Myosin RLC | MYL9 | LC20 | MLC-2C | MLC2 | MMIHS4 | MRLC1 | MYRL2 | 20 kDa myosin
Specifications & PurityExactAb™, Validated, Recombinant, 1.2 mg/mL
Host speciesRabbit
SpecificityMYL9
ImmunogenA synthetic peptide derived from human MYL9 (AA 60-80)
Positive ControlWB: A431, HeLa and U-2 OS cell lysates.
ConjugationUnconjugated
GradeExactAb™, Recombinant, Validated
Product Description

Rabbit anti Human MYL9 Antibody, Recombinant, could be used for WB and so on.
Application:
WB: 1/500-1/1000
Protein Function:
Myosin regulatory subunit that plays an important role in regulation of both smooth muscle and nonmuscle cell contractile activity via its phosphorylation. Implicated in cytokinesis, receptor capping, and cell locomotion.

Product Properties

IsotypeRabbit IgG
Light Chain Typekappa
SDS-PAGE150 kDa
Purification MethodProtein A purified
FormLiquid
Concentration1.2 mg/mL
Storage TempStore at -20°C,Avoid repeated freezing and thawing
Shipped InIce chest + Ice pads
Stability And StorageStore at 4°C short term (1-2 weeks). Store at -20°C long term (24 months). Upon delivery aliquot. Avoid freeze/thaw cycle.

Associated Targets(Human)

MYL9 Tbio Myosin regulatory light polypeptide 9 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Application

ApplicationDilution info
WB

1/500-1/1000

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

Find and download the COA for your product by matching the lot number on the packaging.

2 results found

Lot NumberCertificate TypeDateItem
ZJ24F0708950Certificate of AnalysisJul 29, 2024 Ab116779
ZJ24F0708949Certificate of AnalysisJul 29, 2024 Ab116779

Related Documents

References

1. Deloukas P, Matthews LH, Ashurst J, Burton J, Gilbert JG, Jones M, Stavrides G, Almeida JP, Babbage AK, Bagguley CL, Bailey J, Barlow KF, Bates KN, Beard LM, Beare DM, Beasley OP, Bird CP, Blakey SE, Bridgeman AM, Brown AJ, Buck D, Burrill W, Butler AP, Carder C, Carter NP, Chapman JC, Clamp M, Clark G, Clark LN, Clark SY, Clee CM, Clegg S, Cobley VE, Collier RE, Connor R, Corby NR, Coulson A, Coville GJ, Deadman R, Dhami P, Dunn M, Ellington AG, Frankland JA, Fraser A, French L, Garner P, Grafham DV, Griffiths C, Griffiths MN, Gwilliam R, Hall RE, Hammond S, Harley JL, Heath PD, Ho S, Holden JL, Howden PJ, Huckle E, Hunt AR, Hunt SE, Jekosch K, Johnson CM, Johnson D, Kay MP, Kimberley AM, King A, Knights A, Laird GK, Lawlor S, Lehvaslaiho MH, Leversha M, Lloyd C, Lloyd DM, Lovell JD, Marsh VL, Martin SL, McConnachie LJ, McLay K, McMurray AA, Milne S, Mistry D, Moore MJ, Mullikin JC, Nickerson T, Oliver K, Parker A, Patel R, Pearce TA, Peck AI, Phillimore BJ, Prathalingam SR, Plumb RW, Ramsay H, Rice CM, Ross MT, Scott CE, Sehra HK, Shownkeen R, Sims S, Skuce CD, Smith ML, Soderlund C, Steward CA, Sulston JE, Swann M, Sycamore N, Taylor R, Tee L, Thomas DW, Thorpe A, Tracey A, Tromans AC, Vaudin M, Wall M, Wallis JM, Whitehead SL, Whittaker P, Willey DL, Williams L, Williams SA, Wilming L, Wray PW, Hubbard T, Durbin RM, Bentley DR, Beck S, Rogers J.  (2001)  The DNA sequence and comparative analysis of human chromosome 20..  Nature,  414  (6866): (865-71).  [PMID:11780052]
2. Kumar, C C CC, Mohan, S R SR, Zavodny, P J PJ, Narula, S K SK and Leibowitz, P J PJ..  (1989)  Characterization and differential expression of human vascular smooth muscle myosin light chain 2 isoform in nonmuscle cells..  Biochemistry,    (2):   [PMID:2526655]
3. Iwasaki, T T, Murata-Hori, M M, Ishitobi, S S and Hosoya, H H..  (2001)  Diphosphorylated MRLC is required for organization of stress fibers in interphase cells and the contractile ring in dividing cells..  Cell structure and function,      [PMID:11942626]
4. Tan, Ivan I, Yong, Jeffery J, Dong, Jing Ming JM, Lim, Louis L and Leung, Thomas T..  (2008)  A tripartite complex containing MRCK modulates lamellar actomyosin retrograde flow..  Cell,    (3):   [PMID:18854160]
5. Shoval, Yishay Y, Berissi, Hanna H, Kimchi, Adi A and Pietrokovski, Shmuel S..  (2011)  New modularity of DAP-kinases: alternative splicing of the DRP-1 gene produces a ZIPk-like isoform..  PloS one,    (8):   [PMID:21408167]
6. Tan, Ivan I, Lai, Jesyin J, Yong, Jeffery J, Li, Sam F Y SF and Leung, Thomas T..  (2011)  Chelerythrine perturbs lamellar actomyosin filaments by selective inhibition of myotonic dystrophy kinase-related Cdc42-binding kinase..  FEBS letters,    (6):   [PMID:21457715]
7. Moreno, Carolina Araujo CA and 6 more authors..  (2018)  Homozygous deletion in MYL9 expands the molecular basis of megacystis-microcolon-intestinal hypoperistalsis syndrome..  European journal of human genetics : EJHG,      [PMID:29453416]
8. Kandler, Justin L and 5 more authors..  (2020)  Compound heterozygous loss of function variants in MYL9 in a child with megacystis-microcolon-intestinal hypoperistalsis syndrome..  Molecular genetics & genomic medicine,      [PMID:33031641]

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