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AB3528

Sigma-Aldrich

Anti-Red Fluorescent Protein Antibody

Chemicon®, from chicken

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Synonym(s):
RFP
eCl@ss:
32160702
NACRES:
NA.41

biological source

chicken

Quality Level

antibody form

purified immunoglobulin

antibody product type

primary antibodies

clone

polyclonal

species reactivity (predicted by homology)

all

manufacturer/tradename

Chemicon®

technique(s)

western blot: suitable

UniProt accession no.

shipped in

dry ice

target post-translational modification

unmodified

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This Item
G6795MAB3836MAB10765
antibody form

purified immunoglobulin

antibody form

purified immunoglobulin

antibody form

purified immunoglobulin

antibody form

ascites fluid

biological source

chicken

biological source

mouse

biological source

mouse

biological source

mouse

UniProt accession no.

Q9U6Y8

UniProt accession no.

-

UniProt accession no.

P42212

UniProt accession no.

Q9U6Y8

manufacturer/tradename

Chemicon®

manufacturer/tradename

-

manufacturer/tradename

Chemicon®

manufacturer/tradename

-

clone

polyclonal

clone

GSN24, monoclonal

clone

monoclonal

clone

1DS-1A6, monoclonal

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Specificity

Red fluorescent protein (RFP). Shows no reactivity to GFP.

Immunogen

Recombinant red fluorescent protein (RFP) highly purified by affinity chromatography on Nickel column.

Application

Anti-Red Fluorescent Protein Antibody is an antibody against Red Fluorescent Protein for use in WB.
Immunoblotting: 1:10,000-1:30,000 when detected with an anti-chicken horseradish peroxidase-conjugated secondary by ECL or by a colorimetric assay using DAB.

Optimal working dilutions must be determined by the end user.
Research Category
Epitope Tags & General Use
Research Sub Category
Epitope Tags

Physical form

Format: Purified
Purified immunoglobulin - Ig fraction. Liquid. Buffer = PBS with 0.02% sodium azide

Storage and Stability

Maintain at -20°C in undiluted aliquots for up to 6 months after date of receipt. Avoid repeated freeze/thaw cycles.

Other Notes

Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.

Legal Information

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany

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.

Storage Class

12 - Non Combustible Liquids

wgk_germany

nwg

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificates of Analysis (COA)

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Zhongan Yang et al.
BMC developmental biology, 7, 97-97 (2007-08-22)
GATA-2 is a transcription factor required for hematopoietic stem cell survival as well as for neuronal development in vertebrates. It has been shown that specific expression of GATA-2 in blood progenitor cells requires distal cis-acting regulatory elements. Identification and characterization
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Neuron, 108(3), 512-525 (2020-08-14)
Animals actively sample the sensory world by generating complex patterns of movement that evolve in three dimensions. Whether or how such movements affect neuronal activity in sensory cortical areas remains largely unknown, because most experiments exploring movement-related modulation have been
Carlos P Descovich et al.
eLife, 12 (2023-04-06)
Oriented cell divisions balance self-renewal and differentiation in stratified epithelia such as the skin epidermis. During peak epidermal stratification, the distribution of division angles among basal keratinocyte progenitors is bimodal, with planar and perpendicular divisions driving symmetric and asymmetric daughter
Chitra C Iyer et al.
Human molecular genetics, 24(21), 6160-6173 (2015-08-16)
Spinal Muscular Atrophy (SMA) is an autosomal recessive disorder characterized by loss of lower motor neurons. SMA is caused by deletion or mutation of the Survival Motor Neuron 1 (SMN1) gene and retention of the SMN2 gene. The loss of
Vicki L McGovern et al.
Human molecular genetics, 24(19), 5524-5541 (2015-07-25)
Proximal spinal muscular atrophy (SMA) is the most frequent cause of hereditary infant mortality. SMA is an autosomal recessive neuromuscular disorder that results from the loss of the Survival Motor Neuron 1 (SMN1) gene and retention of the SMN2 gene.

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