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VPS13D Polyclonal antibody

VPS13D Polyclonal Antibody for IF/ICC, WB, ELISA

Host / Isotype

Rabbit / IgG

Reactivity

Human

Applications

IF/ICC, WB, ELISA

Conjugate

Unconjugated

Cat No : 29387-1-AP

Print datasheet

Synonyms

FLJ23066, KIAA0453, VPS13D

验证数据展示

  • WB analysis using 29387-1-AP

    WB analysis using 29387-1-AP

    HeLa cells were subjected to Tris-Acetate gel system followed by western blot with 29387-1-AP (VPS13D antibody) at dilution of 1:500 incubated at room temperature for 1.5 hours.

  • IF Staining of U2OS using 29387-1-AP

    IF Staining of U2OS using 29387-1-AP

    Immunofluorescent analysis of (-20°C Methanol) fixed U2OS cells using VPS13D antibody (29387-1-AP) at dilution of 1:200 and Cy3-conjugated Affinipure Goat Anti-Rabbit IgG(H+L).

经过测试的应用

Positive WB detected inHeLa cells
Positive IF detected inU2OS cells

推荐稀释比

ApplicationDilution
Western Blot (WB)WB : 1:500-1:1000
Immunofluorescence (IF)IF : 1:50-1:500
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.

产品信息

29387-1-AP targets VPS13D in WB, IF, ELISA applications and shows reactivity with Human samples.

Tested Applications IF/ICC, WB, ELISA
Tested Reactivity Human
Immunogen VPS13D fusion protein Ag29933 种属同源性预测
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Full Name vacuolar protein sorting 13 homolog D (S. cerevisiae)
Synonyms FLJ23066, KIAA0453, VPS13D
Calculated Molecular Weight 492 kDa
Observed Molecular Weight~500 kDa
GenBank Accession NumberNM_015378
Gene Symbol VPS13D
Gene ID (NCBI) 55187
Conjugate Unconjugated
Form Liquid
Purification MethodAntigen affinity purification
UNIPROT IDQ5THJ4
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.

背景介绍

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).

实验方案

Product Specific Protocols
WB protocol for VPS13D antibody 29387-1-APDownload protocol
IF protocol for VPS13D antibody 29387-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols