Mouse Monoclonal Crystallin-alphaB antibody [1D11C6E6] (STJ97971)


Reactivity: Human
Applications: WB, IHC, ELISA
Conjugation: Unconjugated
Supplier: St John’s Laboratory Ltd.

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Mouse Monoclonal Crystallin-alphaB antibody [1D11C6E6] (STJ97971)

Supplier: St John’s Laboratory Ltd.

Recommended applications: WB, IHC, ELISA

Recommended dilution: WB 1:500-1:2000; IHC 1:200-1:1000; ELISA 1:10000

Recommended protocols: check protocols

Image descriptions:

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Alternative names:

Check alternative names for the antibody


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 Monoclonal Antibody

Catalogue No.





Crystallin-alphaB Monoclonal Antibody detects endogenous levels of Crystallin-alphaB protein.


Purified recombinant fragment of Crystallin-alphaB (aa1-175) expressed in E Coli





Recommended dilution

WB 1:500-1:2000; IHC 1:200-1:1000; ELISA 1:10000








Crystallin-alphaB Antibody was tube-contained. Ascitic fluid containing 0.03% sodium azide.


1 mg/ml


Crystallin-alphaB Antibody was purified using affinity purification.


-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

Database links

Human UniProt/Swiss-Prot:P02511;Mouse UniPort/Swiss-Prot: P23927;Rat UniProt/Swiss-Port: P23928;Human Entrez Gene: 1410;Mouse Entrez Gene: 12955;Rat Entrez Gene: Rn.98208

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

Research area

All research areas>Kinases and Phosphatases>Alpha B Crystallin
(View all antibody categories related to Kinases and Phosphatases)


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St John’s Laboratory Ltd.

Product type

Primary antibody


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