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Merck
CN

S3195

Anti-SR-A1 antibody produced in rabbit

affinity isolated antibody, ammonium sulfate suspension

Synonym(s):

Anti-Serine Arginine-rich Pre-mRNA Splicing Factor

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About This Item

UNSPSC Code:
12352203
NACRES:
NA.41
MDL number:
MFCD07370515
Conjugate:
unconjugated
Clone:
polyclonal
Application:
IHC, WB
Citations:
2

Key Documents

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biological source

rabbit

conjugate

unconjugated

antibody form

affinity isolated antibody

antibody product type

primary antibodies

clone

polyclonal

form

ammonium sulfate suspension

mol wt

antigen 139.3 kDa

species reactivity

rodent, human

technique(s)

immunohistochemistry: suitable, western blot: suitable

UniProt accession no.

Q9H7N4

storage temp.

−20°C

target post-translational modification

unmodified

Quality Level

200

Gene Information

human ... SCAF1(58506)

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Immunogen

synthetic peptide corresonding to human SR-A1 (amino acids 1203-1216), conjugated to BSA.

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves

Regulatory Information

常规特殊物品
低风险生物材料
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Certificates of Analysis (COA)

Lot/Batch Number
094K1495

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Yujiao Sun et al.
Experimental and therapeutic medicine, 19(6), 3787-3797 (2020-04-30)
The treatment of atherosclerosis remains complex. Pitavastatin serves an important role in the prevention and treatment of atherosclerosis. The present study aimed to investigate the effects of nanoparticle (NP)-mediated delivery of pitavastatin into atherosclerotic plaques as a novel treatment method
Shouta Miyatake et al.
Molecular therapy. Nucleic acids, 14, 520-535 (2019-02-15)
Exon skipping using phosphorodiamidate morpholino oligomers (PMOs) is a promising treatment strategy for Duchenne muscular dystrophy (DMD). The most significant limitation of these clinically used compounds is their lack of delivery systems that target muscles; thus, cell-penetrating peptides are being

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