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SPTAN1 Rabbit Polyclonal Antibody

CAT: 0013-GTR17874827Size: 100 µLDry Ice: NoHazardous: No
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CAT#:0013-GTR17874827Size:100 µL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
Rabbit polyclonal antibody to SPTAN1
Product Name Alternative
DEE5, NEAS, EIEE5, SPTA2
UniProt
Q13813
Reactivity
Human, Mouse
Immunogen
The immunogen is a synthetic peptide directed towards the N terminal region of human SPTAN1
Target
SPTAN1
Clonality
Polyclonal
Conjugation
Unconjugated
Sequence
Synthetic peptide located within the following region: MDPSGVKVLETAEDIQERRQQVLDRYHRFKELSTLRRQKLEDSYRFQFFQ
Field of Research
Neuroscience
Purification
Affinity Purified
Concentration
0.5 mg/ml
Form
Liquid. Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
Molecular Weight
285 kDa
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.
Prediction Reactivity
Bovine, Canine, Equine, Porcine, Rabbit, Rat, Zebrafish
Tested Applications
IHC, IP, WB
NCBI Accession Number
NP_003118
Host or Source
Rabbit
Preservative
Liquid. Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.

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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