VPS13B Polyclonal antibody

VPS13B Polyclonal Antibody for IF, IHC, ELISA

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse

Applications

WB, IF, IHC, ELISA

Conjugate

Unconjugated

Cat no : 24505-1-AP

Synonyms

CHS1, COH1, Cohen syndrome protein 1, KIAA0532, VPS13B



Tested Applications

Positive IHC detected inhuman liver tissue, mouse brain tissue
Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0
Positive IF detected inHepG2 cells

Recommended dilution

ApplicationDilution
Immunohistochemistry (IHC)IHC : 1:50-1:500
Immunofluorescence (IF)IF : 1:10-1:100
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

Product Information

24505-1-AP targets VPS13B in WB, IF, IHC, ELISA applications and shows reactivity with human, mouse samples.

Tested Reactivity human, mouse
Cited Reactivityhuman, mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen VPS13B fusion protein Ag21368
Full Name vacuolar protein sorting 13 homolog B (yeast)
Calculated Molecular Weight 4022 aa, 449 kDa
GenBank Accession NumberBC132978
Gene Symbol VPS13B
Gene ID (NCBI) 157680
RRIDAB_2879579
Conjugate Unconjugated
Form Liquid
Purification MethodAntigen affinity purification
Storage Buffer PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
Storage ConditionsStore at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. 20ul sizes contain 0.1% BSA.

Background Information

VPS13 (vacuolar protein sorting 13 ) acts at membrane contact sites between intracellular organelles to transport lipids. There are four VPS13 family members in human - VPS13A, VPS13B, VPS13C and VPS13D. Mutations in human VPS13 genes are linked to rare neurodegenerative disorders: chorea- acanthocytosis (VPS13A), Cohen syndrome (VPS13B), predispose to early onset into Parkinson disease (VPS13C) and lead to ataxia/spastic paraplegia (VPS13D) (PMID: 30656912).

Protocols

Product Specific Protocols
IHC protocol for VPS13B antibody 24505-1-APDownload protocol
IF protocol for VPS13B antibody 24505-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols

Publications

SpeciesApplicationTitle
mouseIF

Nat Commun

Identification of genes associated with cortical malformation using a transposon-mediated somatic mutagenesis screen in mice.

Authors - I-Ling Lu
mouseIF

Cell Mol Life Sci

Vps13b is required for acrosome biogenesis through functions in Golgi dynamic and membrane trafficking.

Authors - Romain Da Costa
humanWB

bioRxiv

VPS13B is localized at the cis-trans Golgi complex interface and is a functional partner of FAM177A1

Authors - Berrak Ugur