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Merck
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SAB2900809

Sigma-Aldrich

Anti-BCAS1 / NABC1 antibody produced in rabbit

affinity isolated antibody

Sinónimos:

AIBC1, BCAS1, NABC1

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About This Item

UNSPSC Code:
12352203
NACRES:
NA.41

biological source

rabbit

conjugate

unconjugated

antibody form

affinity isolated antibody

antibody product type

primary antibodies

clone

polyclonal

form

buffered aqueous solution

species reactivity

human, mouse

technique(s)

western blot: 1-2 μg/mL (Recombinant Protein)
western blot: 5 μg/mL (Cell Lysate)

UniProt accession no.

O75363

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

Gene Information

human ... BCAS1(8537)

Immunogen

BCAS1 antibody was raised against a 16 amino acid peptide near the carboxy terminus of human BCAS1.
NABC1/BCAS1 antibody was raised against a 16 amino acid peptide near the carboxy terminus of human BCAS1.

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.

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_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Visite la Librería de documentos

Fan Yang et al.
Molecular brain, 12(1), 17-17 (2019-03-15)
Hypomyelination in the central nerves system (CNS) is one of the most obviously pathological features in Niemann-Pick Type C disease (NPC), which is a rare neurodegenerative disorder caused by mutations in the NPC intracellular cholesterol transporter 1 or 2 (Npc1

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