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CLIC2 Mouse Monoclonal Antibody [A5G10] (HA600064)

Price: Regular price $350.00

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Catalog# HA600064

Mouse Monoclonal to CLIC2

Tested for

  • WB

  • IF-Cell

  • IHC-P

  • FC

Reacts with

  • Human

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Specifications

Product Type

Mouse monoclonal primary

Product Name

CLIC2 Mouse Monoclonal Antibody [A5G10] (HA600064)

Immunogen

Recombinant protein within human clic2 aa 50-247 / 247.

Host

Mouse

Positive Control

K562 cell lysates, HepG2, human fetal skeletal muscle tissue, human liver tissue, SH-SY5Y.

Conjugation

Unconjugated

Clonality

Monoclonal

Clone Number

A5G10

RRID

AB_3071681

APPLICATION DILUTION

  • WB

  • 1:500-1:2,000

  • IF-Cell

  • 1:50-1:100

  • IHC-P

  • 1:100-1:500

  • FC

  • 1:100-1:500

PROPERTIES

Form

Liquid

Storage Condition

Store at +4C after thawing. Aliquot store at -20C. Avoid repeated freeze / thaw cycles.

Storage Buffer

1*TBS (pH7.4), 0.2% BSA, 50% Glycerol. Preservative: 0.05% Sodium Azide.

Concentration

2ug/ul

Purification

Protein G affinity purified.

Molecular Weight

28 kDa

Isotype

IgG1

TARGET

UNIPROT #

O15247

PROTEIN NAME

CLIC2

SYNONYMS

Chloride intracellular channel 2 antibody;Chloride intracellular channel protein 2 antibody;CLIC 2b antibody;CLIC2 antibody;CLIC2_HUMAN antibody;CLIC2b antibody;MRXS32 antibody;OTTHUMP00000196471 antibody;XAP 121 antibody;XAP121 antibody

SUBCELLULAR LOCATION

Cytoplasm, Membrane.

FUNCTION

Chloride intracellular channel protein 2 is a protein that in humans is encoded by the CLIC2 gene. Chloride channels are a diverse group of proteins that regulate fundamental cellular processes including stabilization of cell membrane potential, transepithelial transport, maintenance of intracellular pH, and regulation of cell volume. Chloride intracellular channel 2 is a member of the p64 family; the protein is detected in fetal liver and adult skeletal muscle tissue. This gene maps to the candidate region on chromosome X for incontinentia pigmenti. This protein plays a role in inhibiting the function of ryanodine receptor 2. A mutation in this gene is the cause of an X-linked form of cognitive disability.

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