RAB38, Member RAS Oncogene Family (RAB38) Antibody (HRP)

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169€ (20 µg)

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935106861
info@markelab.com
name
RAB38, Member RAS Oncogene Family (RAB38) Antibody (HRP)
category
Primary Antibodies
provider
Abbexa
reference
abx305017
tested applications
ELISA

Description

RAB38 Antibody (HRP) is a Rabbit Polyclonal against RAB38 conjugated to HRP.

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
RAB38, Member RAS Oncogene Family (RAB38)
Host
Rabbit
Reactivity
Human
Recommended Dilution
Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
HRP
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
Tested Applications
ELISA
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
P57729
Gene ID
23682
OMIM
606281
Alias
rrGTPbp,NY-MEL-1,Melanoma antigen NY-MEL-1,Ras-related protein Rab-38
Background
Antibody anti-RAB38
Status
RUO

Descripción

RAB38, member RAS oncogene family (RAB38) is involved in regulating vesicular trafficking, with a primary focus on the sorting and delivery of cargo proteins within the secretory pathway It plays a key role in the movement of vesicles from the Golgi apparatus to other cellular compartments such as the plasma membrane or lysosomes, which are essential for proper cell function and membrane recycling RAB38 is involved in the maintenance of cell signaling by regulating the trafficking of receptor proteins and enzymes, ensuring their correct localization and function Additionally, RAB38 participates in autophagy, a critical cellular process for degrading and recycling cellular components RAB38’s dysfunction is associated with disorders related to impaired vesicular trafficking, including certain types of cancer and neurodegenerative diseases where disturbed cellular function contributes to pathological changes

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