KLC2 Rabbit pAb (APR23964N)

CAT: 0882-APR23964N-01Size: 50 µLDry Ice: NoHazardous: No

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CAT#:0882-APR23964N-01Size:50 µL

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24/48H Stock Items & 2 to 6 Weeks non Stock Items.

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Background

The protein encoded by this gene is a light chain of kinesin, a molecular motor responsible for moving vesicles and organelles along microtubules. Defects in this gene are a cause of spastic paraplegia, optic atrophy, and neuropathy (SPOAN) syndrome. [provided by RefSeq, Mar 2016]

Overview

We constantly strive to ensure we provide our customers with the best antibodies. As a result of this work we offer this antibody in purified format. We are in the process of updating our datasheets. If you have any questions regarding this update, please feel free to contact our technical support team. This product is a high quality KLC2 Rabbit pAb (APR23964N) .

Synonyms

KLC2; SPOAN

Gene ID

64837

UniProt

Q9H0B6

Dilution

WB 1:500 - 1:2000

Form

Liquid

Buffer

Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

Molecular Weight

Calculated MW: 60kDa/68kDa Observed MW: 69kDa

Storage Conditions

Store at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

Gene ID URL

https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=gene&cmd=Retrieve&dopt=Graphics&list_uids=64837

Uniprot URL

https://www.uniprot.org/uniprot/Q9H0B6

AA Sequence

MAMMVFPREEKLSQDEIVLGTKAVIQGLETLRGEHRALLAPLVAPEAGEAEPGSQERCILLRRSLEAIELGLGEAQVILALSSHLGAVES

UniProtKB · Q9H0B6

Kinesin light chain 2

KLC2_HUMAN · Homo sapiens

View on UniProt ↗

Primary accession: Q9H0B6
Review status: UniProtKB reviewed (Swiss-Prot)
Gene: KLC2
Protein existence: 1: Evidence at protein level
Organism: Homo sapiens (Human)
Taxonomy ID: 9606
Alternative names: KLC 2
EC number: —
Processing: —
Secondary accessions: A8MXL7, B2RDY4, Q9H9C8, Q9HA20

Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Coding sequence diversity

Alternative splicing

Domain

Coiled coilRepeatTPR repeat

Cellular component

CytoplasmCytoskeletonLysosomeMembraneMicrotubule

Disease

Hereditary spastic paraplegiaNeurodegenerationNeuropathy

Molecular function

Motor protein

PTM

Phosphoprotein

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