Human CRYAA (Alpha-crystallin A chain) ELISA Kit

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935106861
info@markelab.com
name
Human CRYAA (Alpha-crystallin A chain) ELISA Kit
category
ELISA Kits
provider
FineTest
reference
EH1621
tested applications
ELISA

Documents del producto

Instrucciones
Descargar
Data sheet

Product specifications

Category
ELISA Kits
Reactivity
Human
Detection Method
Colorimetric
Assay Data
4 hours
Assay Type
Sandwich ELISA, Double Antibody
Test Range
0.781-50ng/ml
Sensitivity
0.469ng/ml
Size 1
96T
Tested Applications
ELISA
Sample Type
Serum, Plasma, Cell Culture Supernatant, cell or tissue lysate, Other liquid samples
Availability
Shipped within 10-14 working days.
Storage
2-8 °C for 12 months
UniProt ID
P02489
Alias
Alpha-crystallin A chain, Heat shock protein beta-4, HspB4, Alpha-crystallin A(1-172, Alpha-crystallin A(1-168, Alpha-crystallin A(1-162, CRYAA, CRYA1, HSPB4
Background
Elisa kits for CRYAA
Status
RUO

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Alpha-Crystallin A Chain (CRYAA) Antibody

CRYAA Antibody is a Rabbit Polyclonal antibody against CRYAA. Mammalian lens crystallins are divided into alpha, beta, and gamma families. Alpha crystallins are composed of two gene products: alpha-A and alpha-B, for acidic and basic, respectively. Alpha crystallins can be induced by heat shock and are members of the small heat shock protein (HSP20) family. They act as molecular chaperones although they do not renature proteins and release them in the fashion of a true chaperone; instead they hold them in large soluble aggregates. Post-translational modifications decrease the ability to chaperone. These heterogeneous aggregates consist of 30-40 subunits; the alpha-A and alpha-B subunits have a 3:1 ratio, respectively. Two additional functions of alpha crystallins are an autokinase activity and participation in the intracellular architecture. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. Alpha-A and alpha-B gene products are differentially expressed; alpha-A is preferentially restricted to the lens and alpha-B is expressed widely in many tissues and organs. Defects in this gene cause autosomal dominant congenital cataract (ADCC).

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