COH1 Antilichaam
Gecertificeerd

COH1 Antilichaam

Catalog #: 6931-01
Maat: 0.02 mg

Kwaliteit

ISO Gecertificeerd

Levering

24-48 uur

Prijs -1%
Login voor prijs
BTW niet inbegrepen
Gratis verzending vanaf €100
Technische Documentatie

Technische Specificaties

Background

COH1 Antibody: COH1 (Cohen syndrome protein 1), also known as VPS13B (vacuolar protein sorting-associated protein 13B) or CHS1, belongs to the VPS13 family and may function in vesicle-mediated transport and sorting of proteins within the cell. COH1 is widely expressed and multiple alternatively spliced transcript variants have been observed. Mutations in this gene have been associated with Cohen syndrome. COH1 is a Golgi-localized peripheral membrane protein and plays a critical role in Golgi (re) assembly.

NCBI Gene ID

157680

Swiss Prot

Q7Z7G8

Accession Number

NP_056058

Host

• Rabbit

Reactivity

Human, Mouse, Rat

Clonality

• Polyclonal

Conjugation

Unconjugated

Type

Primary Antibodies

Field of Research

Homeostasis

Purification

COH1 Antibody is affinity chromatography purified via peptide column.

Positive Control

Cat. No. 1220 - SK-N-SH Cell Lysate

Concentration

1 mg/mL

Buffer

COH1 Antibody is supplied in PBS containing 0.02% sodium azide.

Modification

None

Shipping Conditions

Blue Ice

Storage Conditions

COH1 antibody can be stored at 4˚ C for three months and -20˚ C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Fragment

IgG

Specificity

At least five alternatively spliced transcript variants have been observed. COH1 detects two isoforms.

Symbol

VPS13B

Positive Control 2

Cat. No. 10-301 - Human Brain Tissue Slide

NCBI Official Name

Vacuolar protein sorting 13 homolog B (yeast)

NCBI Organism

Homo sapiens

Background Reference 01

Velayos-Baeza A, Vettori A, Copley RR, et al. Analysis of the human VPS13 gene family. Genomics 2004; 84:536-49.

Background Reference 02

Kolehmainen J, Black GC, Saarinen A, et al. Cohen syndrome is caused by mutations in a novel gene, COH1, encoding a transmembrane protein with a presumed role in vesicle-mediated sorting and intracellular protein transport. Am. J. Hum. Genet. 2003; 72:1359-69.

Background Reference 03

Seifert W, Kühnisch J, Maritzen T, et al. Cohen syndrome-associated protein, COH1, is a novel, giant Golgi matrix protein required for Golgi integrity. J. Biol. Chem. 2011; 286:37665-75.

Other Product Names

COH1 Antibody: CHS1, COH1, CHS1, KIAA0532, Vacuolar protein sorting-associated protein 13B, Cohen syndrome protein 1

Tested Applications

ELISA, WB, IF

Protein ID

35493725

Physical Properties

Liquid

Beschrijving

COH1 Antilichaam Beschikbaar in 0.02 mg. Bestel eenvoudig online met snelle levering.

Specificaties

ProductnaamCOH1 Antilichaam
Categorie
Beschikbare grootte0.02 mg
Catalogusnummer6931-01