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SAB4300571

Sigma-Aldrich

Anti-MAP1LC3A antibody

rabbit polyclonal

Synonym(s):

Anti-LC3 antibody produced in rabbit, Anti-LC3A antibody produced in rabbit, Anti-MAP1ALC3 antibody produced in rabbit, Anti-MAP1BLC3 antibody produced in rabbit, Anti-microtubule-associated protein 1 light chain 3 alpha antibody produced in rabbit

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About This Item

UNSPSC Code:
12352203
NACRES:
NA.41

product name

Anti-MAP1LC3A antibody produced in rabbit, affinity isolated antibody

biological source

rabbit

Quality Level

100

conjugate

unconjugated

antibody form

affinity isolated antibody

antibody product type

primary antibodies

clone

polyclonal

form

buffered aqueous solution

mol wt

~16 kDa
 ~18 kDa

species reactivity

rat, human, mouse

concentration

1 mg/mL

technique(s)

indirect immunofluorescence: 1:100-1:200
western blot: 1:500-1:1000

isotype

IgG

immunogen sequence

(R-P-F-K-Q)

NCBI accession no.

NP_115903.1

UniProt accession no.

Q9H492

shipped in

wet ice

storage temp.

−20°C

target post-translational modification

unmodified

Gene Information

human ... MAP1LC3A(84557)

Immunogen

Peptide sequence around aa. 5-10 (R-P-F-K-Q), according to the protein MAP1LC3A.

Features and Benefits

Evaluate our antibodies with complete peace of mind. If the antibody does not perform in your application, we will issue a full credit or replacement antibody. Learn more.

Target description

Probably involved in formation of autophagosomal vacuoles (autophagosomes).

Physical form

Solution in phosphate-buffered saline containing 0.02% sodium azide and 50% glycerol

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 Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Cell death & disease, 8(12), 3223-3223 (2017-12-21)
Spinal muscular atrophy (SMA) is a recessive autosomal neuromuscular disease, due to homozygous mutations or deletions in the telomeric survival motoneuron gene 1 (SMN1). SMA is characterized by motor impairment, muscle atrophy, and premature death following motor neuron (MN) degeneration.

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