Products for Research Use Only

SPTAN1 Antibody

CAT: 0013-GTR18194436-01Size: 20 µgDry Ice: NoHazardous: No
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CAT#:0013-GTR18194436-01Size:20 µg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
Mouse monoclonal antibody to Fodrin / Alpha Spectrin II (SPTAN1) / NEAS
Product Name Alternative
Alpha-II spectrin; brain; EIEE5; Fodrin alpha chain; NEAS; Non erythrocytic spectrin alpha; non-erythroid alpha chain; SPECA; Spectrin alpha chain brain; Spectrin, alpha, non-erythrocytic 1 (alpha-fodrin) ; Spna2; SPTA2
UniProt
Q13813
Reactivity
Human
Immunogen
Recombinant fragment of human SPTAN1 protein (around aa 2351-2475) (exact sequence is proprietary)
Target
SPTAN1
Clonality
Monoclonal
Clone
SPTAN1/3351
Conjugation
Unconjugated
Field of Research
Neuroscience
Purification
Protein A
Form
200ug/ml of Ab Purified from Bioreactor Concentrate by Protein A/G. Prepared in 10mM PBS with 0.05% rAlbumin & 0.05% azide. Also available WITHOUT rAlbumin & azide at 1.0mg/ml.
Molecular Weight
240kDa
Storage Conditions
Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Notes
For research use only.
Tested Applications
IHC
Host or Source
Mouse
Isotype
IgG2b

UniProtKB · Q13813

Spectrin alpha chain, non-erythrocytic 1

SPTN1_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q13813
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
SPTAN1
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
—
Secondary accessions
Q13186, Q15324, Q16606, Q59EF1, Q5VXV5, Q5VXV6, Q7Z6M5, Q9P0V0
Protein keywords

Technical term

3D-structureDirect protein sequencingProteomics identificationReference proteome

PTM

AcetylationPhosphoprotein

Molecular function

Actin cappingActin-bindingCalmodulin-binding

Coding sequence diversity

Alternative splicing

Ligand

CalciumMetal-binding

Cellular component

CytoplasmCytoskeleton

Disease

Disease variantEpilepsyHereditary spastic paraplegiaIntellectual disabilityNeurodegenerationNeuropathy

Domain

RepeatSH3 domain

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