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ALG9 Polyclonal Antibody

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ALG9 Polyclonal Antibody

ALG9 Polyclonal Antibody

Size: 200μL

Storage: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.

Shipping: The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.

Exp date: 12 months

Category ID_II: Primary Antibodies

Category ID_III: Polyclonal Antibodies

Abbreviation: ALG9

Target Synonym: ALG9;ALG9;Alpha-1;2-mannosyltransferase ALG9;Asparagine-linked glycosylation protein 9 homolog;Disrupted in bipolar disorder protein 1

Research Areas:

Conjugation: Unconjugated

Host: Rabbit

Species reactivity: Human;Mouse

Application: IHC

Isotype: IgG

Clonality: Polyclonal

Clone NO.:

UNIProt ID: Q9H6U8

Accession:

Background: This gene encodes an alpha-1,2-mannosyltransferase enzyme that functions in lipid-linked oligosaccharide assembly. Mutations in this gene result in congenital disorder of glycosylation type Il. Multiple transcript variants encoding different isoforms have been found for this gene.

Concentration: 0.1 mg/mL

Immunogen: Recombinant protein of human ALG9

Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4

Purification method: Affinity purification

Dilution: IHC 1:50-1:200

Calculated MW:

ObservedMW:

$460.42

Original: $1,534.73

-70%
ALG9 Polyclonal Antibody

$1,534.73

$460.42

Product Information

Shipping & Returns

Description

Size: 200μL

Storage: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.

Shipping: The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.

Exp date: 12 months

Category ID_II: Primary Antibodies

Category ID_III: Polyclonal Antibodies

Abbreviation: ALG9

Target Synonym: ALG9;ALG9;Alpha-1;2-mannosyltransferase ALG9;Asparagine-linked glycosylation protein 9 homolog;Disrupted in bipolar disorder protein 1

Research Areas:

Conjugation: Unconjugated

Host: Rabbit

Species reactivity: Human;Mouse

Application: IHC

Isotype: IgG

Clonality: Polyclonal

Clone NO.:

UNIProt ID: Q9H6U8

Accession:

Background: This gene encodes an alpha-1,2-mannosyltransferase enzyme that functions in lipid-linked oligosaccharide assembly. Mutations in this gene result in congenital disorder of glycosylation type Il. Multiple transcript variants encoding different isoforms have been found for this gene.

Concentration: 0.1 mg/mL

Immunogen: Recombinant protein of human ALG9

Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4

Purification method: Affinity purification

Dilution: IHC 1:50-1:200

Calculated MW:

ObservedMW: