Products for Research Use Only

ISPD Antibody

CAT: 0013-GTR17905866-02Size: 100 µgDry Ice: NoHazardous: No
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CAT#:0013-GTR17905866-02Size:100 µg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
This ISPD Antibody is an unconjugated polyclonal product. It tagets ISPD using a Recombinant Human Isoprenoid synthase domain-containing protein (1-264AA) as the immunogen. This antibody is suitable for ELISA, IF, IHC. Purification: >95%, Protein G purified.
Product Name Alternative
2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase-like protein antibody; Isoprenoid synthase domain-containing protein antibody; ispD antibody; ISPD_HUMAN antibody
UniProt
A4D126
Reactivity
Human
Immunogen
Recombinant Human Isoprenoid synthase domain-containing protein (1-264AA)
Target
ISPD
Clonality
Polyclonal
Conjugation
Unconjugated
Purification
>95%, Protein G purified
Dilution
IHC-P:1:20-200, IF:1:50-200
Form
Liquid
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
ELISA, IF, IHC
Host or Source
Rabbit
Preservative
Preservative: 0.03% Proclin 300. Constituents: 50% Glycerol
Isotype
IgG

UniProtKB · A4D126

D-ribitol-5-phosphate cytidylyltransferase

ISPD_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
A4D126
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
CRPPA
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
2.7.7.40
Processing
—
Secondary accessions
A8MU35, H9KVB2
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Coding sequence diversity

Alternative splicing

Disease

Congenital muscular dystrophyDisease variantDystroglycanopathyLimb-girdle muscular dystrophyLissencephaly

Cellular component

Cytoplasm

Molecular function

NucleotidyltransferaseTransferase

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