• IHC staining of FFPE human skeletal muscle with CACNA1S antibody. HIER: boil tissue sections in pH8 EDTA for 20 min and allow to cool before testing.
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NSJ Bioreagents

RQ6164

CACNA1S Antibody

CACNA1S Antibody

$449.00 USD
$449.00 USD
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Cav1.1 also known as the calcium channel, voltage-dependent, L type, alpha 1S subunit, (CACNA1S), is a protein which in humans is encoded by the CACNA1S gene. This gene encodes one of the five subunits of the slowly inactivating L-type voltage-dependent calcium channel in skeletal muscle cells. Mutations in this gene have been associated with hypokalemic periodic paralysis, thyrotoxic periodic paralysis and malignant hyperthermia susceptibility.

Specifications

Family Primary antibody
Formulation 0.5mg/ml if reconstituted with 0.2ml sterile DI water
Format Antigen affinity purified
Host Animal Rabbit
Clonality Polyclonal (rabbit origin)
Isotype Rabbit IgG
Species Reactivity Human, Mouse, Rat, Monkey
Application WB, IHC-P, FACS, Direct ELISA
Application Details Western blot: 1-2ug/ml,Immunohistochemistry (FFPE): 2-5ug/ml,Flow cytometry: 1-3ug/million cells,Direct ELISA: 0.1-0.5ug/ml
Application Note Optimal dilution of the CACNA1S antibody should be determined by the researcher.
Immunogen A human recombinant partial protein (amino acids E1583-C1779) was used as the immunogen for the CACNA1S antibody.
Buffer Lyophilized from 1X PBS with 2% Trehalose and 0.0125% sodium azide
Purity Affinity purified
Storage After reconstitution, the CACNA1S antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
Limitation This CACNA1S antibody is available for research use only.
Uniprot # Q13698
Status Available
PDF Link https://www.nsjbio.com/tds-pdf/cacna1s-antibody-rq6164
Title CACNA1S Antibody
Description Cav1.1 also known as the calcium channel, voltage-dependent, L type, alpha 1S subunit, (CACNA1S), is a protein which in humans is encoded by the CACNA1S gene. This gene encodes one of the five subunits of the slowly inactivating L-type voltage-dependent calcium channel in skeletal muscle cells. Mutations in this gene have been associated with hypokalemic periodic paralysis, thyrotoxic periodic paralysis and malignant hyperthermia susceptibility.
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