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Rabbit Polyclonal Phospho-Crystallin-alphaB (S45) antibody (STJ90896)
Supplier: St John’s Laboratory Ltd.
Recommended applications: WB, IHC, ELISA
Recommended dilution: WB 1:500-1:2000; IHC 1:100-1:300; ELISA 1:10000;
Recommended protocols: check protocols
Click or hover above images to see image description for Crystallin-alphaB (phospho Ser45) Polyclonal Antibody.
Check alternative names for the antibodyExpand
CRYAB antibody, CRYA2 antibody, HSPB5 antibody,|AACRYA antibody|Alpha B crystallin antibody|Alpha crystallin B chain antibody|Alpha(B)-crystallin antibody|Alpha-crystallin B chain antibody|CRYA2 antibody|Cryab antibody|CRYAB_HUMAN antibody|Crystallin alpha B antibody|Crystallin alpha polypeptide 2 antibody|CTPP2 antibody|Heat shock 20 kD like protein antibody|Heat shock protein beta 5 antibody|Heat shock protein beta-5 antibody|HspB5 antibody|Renal carcinoma antigen NY REN 27 antibody|Renal carcinoma antigen NY-REN-27 antibody|Rosenthal fiber component antibody|Anti-Alpha B Crystallin antibody [1B6.1-3G4] (ab13496)
SCBT cat No: sc-365088|sc-137143|sc-398079|sc-137144|sc-137129|sc-22744|sc-22391|sc-51745|sc-398395|sc-134243|
Crystallin-alphaB (phospho Ser45) Polyclonal Antibody
|Catalogue No.|| |
Human, Mouse, Rat, Monkey
Phospho-Crystallin-alphaB (S45) Polyclonal Antibody detects endogenous levels of Crystallin-alphaB protein only when phosphorylated at S45.
Synthesized phospho-peptide derived from Crystallin-alphaB (phospho Ser45) at AA range 40-120
WB, IHC, ELISA
|Recommended dilution|| |
WB 1:500-1:2000; IHC 1:100-1:300; ELISA 1:10000;
|Molecular weight|| |
Crystallin-alphaB (phospho Ser45) Antibody was tube-contained. Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Crystallin-alphaB (phospho Ser45) Antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
-20 Celsius degree. Avoid repeated freeze/thaw cycles.
|Alternative antibody names|| |
Alpha-crystallin B chain antibody, Alphaantibody, B antibody,-crystallin antibody, Heat shock protein beta-5 antibody, HspB5 antibody, Renal carcinoma antigen NY-REN-27 antibody, Rosenthal fiber component antibody
|Protein names|| |
Alpha-crystallin B chain , Alpha, B ,-crystallin , Heat shock protein beta-5 , HspB5 , Renal carcinoma antigen NY-REN-27 , Rosenthal fiber component
|Protein function|| |
May contribute to the transparency and refractive index of the lens. Has chaperone-like activity, preventing aggregation of various proteins under a wide range of stress conditions.
|Protein tissue specificity|| |
Lens as well as other tissues.
|Involvement in disease|| |
Myopathy, myofibrillar, 2 (MFM2) [MIM:608810]: A neuromuscular disorder that results in weakness of the proximal and distal limb muscles, weakness of the neck, velopharynx and trunk muscles, hypertrophic cardiomyopathy, and cataract in a subset of patients. . Note: The disease is caused by mutations affecting the gene represented in this entry.; Cataract 16, multiple types (CTRCT16) [MIM:613763]: An opacification of the crystalline lens of the eye that frequently results in visual impairment or blindness. Opacities vary in morphology, are often confined to a portion of the lens, and may be static or progressive. In general, the more posteriorly located and dense an opacity, the greater the impact on visual function. CTRCT16 includes posterior polar cataract, among others. Posterior polar cataract is a subcapsular opacity, usually disk-shaped, located at the back of the lens. . Note: The disease is caused by mutations affecting the gene represented in this entry.; Myopathy, myofibrillar, fatal infantile hypertonic, alpha-B crystallin-related (MFMFIH-CRYAB) [MIM:613869]: A muscular dystrophy with onset in the first weeks of life after a normal neonatal period. Affected infants show rapidly progressive muscular rigidity of the trunk and limbs associated with increasing respiratory difficulty resulting in death before age 3 years. . Note: The disease is caused by mutations affecting the gene represented in this entry.; Cardiomyopathy, dilated 1II (CMD1II) [MIM:615184]: A disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death. . Note: The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the small heat shock protein (HSP20) family.
|Protein cellular localization|| |
Cytoplasm / Nucleus
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St John’s Laboratory Ltd.
|Product type|| |
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