DENND5A Antibody (FITC)

Este producto es parte de DENND - DENN domain containing
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169€ (20 µg)

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935106861
info@markelab.com
name
DENND5A Antibody (FITC)
category
Primary Antibodies
provider
Abbexa
reference
abx308009

Description

DENND5A Antibody (FITC) is a Rabbit Polyclonal against DENND5A conjugated to FITC.

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
DENND5A
Host
Rabbit
Reactivity
Human
Recommended Dilution
Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
FITC
Isotype
IgG
Purity
> 95%
Purification
Purified by Protein G.
Size 1
20 µg
Size 2
50 µg
Size 3
100 µg
Size 4
200 µg
Size 5
1 mg
Form
Liquid
Buffer
0.01 M PBS, pH 7.4, 0.03% Proclin-300 and 50% Glycerol.
Availability
Shipped within 5-10 working days.
Storage
Aliquot and store at -20°C. Avoid exposure to light. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
Q6IQ26
Gene ID
23258
NCBI Accession
NP_001230183.1, NM_001243254.1, NP_001335677.1, NM_001348748.1
OMIM
617278
Alias
DEE49,EIEE49,RAB6IP1,Rab6-interacting protein 1
Background
Antibody anti-DENND5A
Status
RUO

Descripción

DENN domain containing 5A (DENND5A) is a member of the DENN domain protein family, functioning as a guanine nucleotide exchange factor (GEF) for Rab GTPases, particularly Rab39. DENND5A plays a vital role in regulating endosomal trafficking, exocytosis, and lysosomal function by activating Rab39 through GDP-to-GTP exchange. This activity is critical for vesicular transport and recycling of proteins, such as receptors and ion channels, involved in signaling and nutrient uptake. DENND5A also contributes to autophagy by mediating the trafficking and fusion of autophagosomes and lysosomes, which are essential for the degradation of damaged organelles and proteins. It is expressed ubiquitously, with higher levels in tissues undergoing rapid turnover or high trafficking demands, such as neurons and epithelial cells. Dysregulation of DENND5A has been associated with neurological disorders and lysosomal storage diseases, where defects in vesicle transport disrupt cellular proteostasis and signaling pathways. Further research into its specific substrates and pathways may uncover additional roles in maintaining cellular health.

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